Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7371 |
| ensemblid | ENSG00000143179.16 |
| hgncid | 12562 |
| symbol | UCK2 |
| name | uridine-cytidine kinase 2 |
| refseq_nuc | NM_012474.5 |
| refseq_prot | NP_036606.2 |
| ensembl_nuc | ENST00000367879.9 |
| ensembl_prot | ENSP00000356853.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 165827614 |
| end | 165911618 |
| strand | + |
| ver | v1.2 |
| region | chr1:165827614-165911618 |
| region5000 | chr1:165822614-165916618 |
| regionname0 | UCK2_chr1_165827614_165911618 |
| regionname5000 | UCK2_chr1_165822614_165916618 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 261 | 319 | 89 | 62 | 120 | 14 | 34 | 94 | UCK2_chr1_165822614_165916618 | UCK2 | MAGDS others(256): Show |
chr1 | 165822614 | 165916618 |
| a0002 | 0/0 | 261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | MAGDS others(256): Show |
chr1 | 165822614 | 165916618 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 783 | 295 | 88 | 57 | 105 | 13 | 32 | UCK2_chr1_165822614_165916618 | UCK2 | ATGGC others(778): Show |
chr1 | 165822614 | 165916618 | ||
| a0001c0002 | 0/0 | 783 | 24 | 1 | 5 | 15 | 1 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | ATGGC others(778): Show |
chr1 | 165822614 | 165916618 | ||
| a0002c0003 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | ATGGC others(778): Show |
chr1 | 165822614 | 165916618 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4801 | 89 | 6 | 26 | 45 | 4 | 8 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0002 | 0/0 | 4800 | 43 | 11 | 10 | 8 | 4 | 10 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0003 | 0/0 | 4800 | 33 | 0 | 8 | 19 | 1 | 5 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0004 | 0/0 | 4800 | 29 | 16 | 2 | 10 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0005 | 0/0 | 4800 | 2 | 0 | 2 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0006 | 0/0 | 4800 | 22 | 22 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0007 | 0/0 | 4800 | 15 | 2 | 6 | 0 | 2 | 5 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0008 | 0/0 | 4801 | 10 | 0 | 3 | 4 | 0 | 3 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0009 | 0/0 | 4800 | 8 | 8 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0010 | 0/0 | 4800 | 6 | 0 | 0 | 6 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0011 | 0/0 | 4800 | 6 | 0 | 0 | 6 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0012 | 0/0 | 4801 | 4 | 4 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0013 | 0/0 | 4800 | 3 | 3 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0014 | 0/0 | 4800 | 3 | 0 | 0 | 3 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0016 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0017 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0018 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0019 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0021 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0022 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0023 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0024 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0025 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0026 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0027 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0028 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0029 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0030 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0031 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0032 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0033 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0035 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0036 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0001t0037 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4796): Show |
chr1 | 165822614 | 165916618 |
| a0001c0002t0005 | 0/0 | 4800 | 20 | 1 | 4 | 12 | 1 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0002t0015 | 0/0 | 4800 | 2 | 0 | 0 | 2 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0002t0020 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0001c0002t0034 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| a0002c0003t0009 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | GTAAA others(4795): Show |
chr1 | 165822614 | 165916618 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0010g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0011g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0011g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0013g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0013g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0013g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0014g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0014g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0016g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0016g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0017g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0019g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0021g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0022g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0023g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0024g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0025g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0026g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0027g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0028g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0029g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0030g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0031g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0032g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0033g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0035g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0036g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0001t0037g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0015g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0015g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0020g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0001c0002t0034g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| a0002c0003t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0267 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0023 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0171 | EUR | FIN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0263 | EUR | FIN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0271 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0265 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01106 | hp1 | a0001 | c0002 | t0005 | g0125 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01175 | hp2 | a0001 | c0002 | t0005 | g0101 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0269 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0255 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0082 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0264 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0129 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0140 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01515 | hp1 | a0001 | c0001 | t0032 | g0259 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0161 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0117 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0153 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02040 | hp2 | a0001 | c0002 | t0005 | g0186 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0292 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02080 | hp1 | a0001 | c0002 | t0005 | g0099 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02129 | hp1 | a0001 | c0002 | t0005 | g0226 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02132 | hp2 | a0001 | c0001 | t0010 | g0258 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02135 | hp1 | a0001 | c0001 | t0010 | g0247 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02135 | hp2 | a0001 | c0002 | t0005 | g0224 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0301 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02155 | hp2 | a0001 | c0002 | t0005 | g0305 | EAS | CDX | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02257 | hp1 | a0001 | c0001 | t0023 | g0300 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0315 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0037 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02300 | hp1 | a0001 | c0002 | t0034 | g0126 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02451 | hp1 | a0001 | c0001 | t0036 | g0136 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0079 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02572 | hp2 | a0001 | c0001 | t0022 | g0293 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02602 | hp1 | a0001 | c0002 | t0005 | g0081 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0105 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0280 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02809 | hp1 | a0001 | c0001 | t0029 | g0132 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0063 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0288 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0062 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0014 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02976 | hp2 | a0001 | c0001 | t0017 | g0004 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0276 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0012 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0296 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03195 | hp2 | a0001 | c0001 | t0016 | g0066 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03209 | hp1 | a0001 | c0001 | t0021 | g0135 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0282 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0127 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03453 | hp1 | a0001 | c0001 | t0027 | g0084 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0285 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0072 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0071 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03516 | hp1 | a0001 | c0001 | t0017 | g0004 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0083 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03540 | hp2 | a0002 | c0003 | t0009 | g0080 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0116 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03579 | hp2 | a0001 | c0001 | t0016 | g0286 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0022 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0060 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03927 | hp1 | a0001 | c0001 | t0030 | g0051 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04199 | hp1 | a0001 | c0002 | t0005 | g0088 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0090 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0103 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18747 | hp1 | a0001 | c0002 | t0020 | g0198 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18941 | hp2 | a0001 | c0002 | t0015 | g0225 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18944 | hp2 | a0001 | c0001 | t0011 | g0253 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0232 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18956 | hp1 | a0001 | c0001 | t0018 | g0196 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18957 | hp1 | a0001 | c0001 | t0011 | g0220 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18960 | hp1 | a0001 | c0002 | t0005 | g0141 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18964 | hp1 | a0001 | c0001 | t0026 | g0240 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18964 | hp2 | a0001 | c0001 | t0035 | g0199 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0093 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18980 | hp1 | a0001 | c0002 | t0005 | g0035 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18983 | hp2 | a0001 | c0002 | t0005 | g0147 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18984 | hp2 | a0001 | c0001 | t0010 | g0261 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18993 | hp2 | a0001 | c0002 | t0005 | g0146 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19000 | hp1 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19000 | hp2 | a0001 | c0002 | t0005 | g0235 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19005 | hp1 | a0001 | c0001 | t0011 | g0040 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19009 | hp1 | a0001 | c0001 | t0011 | g0145 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0252 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19030 | hp1 | a0001 | c0001 | t0025 | g0275 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0134 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19056 | hp2 | a0001 | c0002 | t0005 | g0183 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19062 | hp1 | a0001 | c0001 | t0014 | g0018 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19064 | hp2 | a0001 | c0001 | t0031 | g0231 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19065 | hp2 | a0001 | c0002 | t0005 | g0077 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19068 | hp2 | a0001 | c0001 | t0011 | g0244 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19070 | hp2 | a0001 | c0002 | t0015 | g0248 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19086 | hp2 | a0001 | c0001 | t0014 | g0019 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19091 | hp1 | a0001 | c0001 | t0014 | g0020 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19091 | hp2 | a0001 | c0001 | t0010 | g0170 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0290 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ASW | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | ASW | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0128 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20805 | hp2 | a0001 | c0002 | t0005 | g0057 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0091 | SAS | GIH | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0030 | SAS | GIH | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0281 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02486 | hp1 | a0001 | c0001 | t0028 | g0106 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02559 | hp1 | a0001 | c0001 | t0033 | g0010 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG02559 | hp2 | a0001 | c0001 | t0037 | g0287 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0277 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA21309 | hp1 | a0001 | c0001 | t0024 | g0078 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:165891238 | A | G | 1 | a0002 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.272A>G | p.Asn91Ser | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/7 | 492/4801 | 272/786 | 91/261 | chr1 | 165891238 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:165896241 | G | A | 1 | a0001c0002 | 24 | HG01106.hp1 HG01175.hp2 HG01192.hp1 others(21): Show |
synonymous_variant | LOW | c.408G>A | p.Gly136Gly | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/7 | 628/4801 | 408/786 | 136/261 | chr1 | 165896241 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:165827669 | C | T | 2 | a0001c0001t0017 a0001c0001t0037 |
3 | HG02559.hp2 HG02976.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-165C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/7 | 165 | chr1 | 165827669 | ||||||
| chr1:165827819 | G | C | 1 | a0001c0001t0018 | 1 | NA18956.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/7 | 15 | chr1 | 165827819 | ||||||
| chr1:165907909 | A | G | 1 | a0001c0001t0036 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 86 | chr1 | 165907909 | ||||||
| chr1:165908040 | A | G | 1 | a0001c0001t0035 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 217 | chr1 | 165908040 | ||||||
| chr1:165908102 | A | T | 2 | a0001c0001t0011 a0001c0002t0034 |
7 | HG02300.hp1 NA18944.hp2 NA18957.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*279A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 279 | chr1 | 165908102 | ||||||
| chr1:165908338 | A | C | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(9): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*515A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 515 | chr1 | 165908338 | ||||||
| chr1:165908423 | T | C | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*600T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 600 | chr1 | 165908423 | ||||||
| chr1:165908433 | CT | C | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(28): Show |
212 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*622delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 622 | INFO_REALIGN_3_PRIME | chr1 | 165908433 | |||||
| chr1:165908514 | G | A | 5 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0015 others(2): Show |
26 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 691 | chr1 | 165908514 | ||||||
| chr1:165908552 | C | T | 2 | a0001c0001t0007 a0001c0001t0032 |
16 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*729C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 729 | chr1 | 165908552 | ||||||
| chr1:165908751 | G | A | 1 | a0001c0001t0032 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 928 | chr1 | 165908751 | ||||||
| chr1:165908753 | C | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 930 | chr1 | 165908753 | ||||||
| chr1:165908909 | C | T | 1 | a0001c0001t0031 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1086 | chr1 | 165908909 | ||||||
| chr1:165909038 | A | C | 1 | a0001c0001t0010 | 6 | HG02132.hp2 HG02135.hp1 NA18979.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1215A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1215 | chr1 | 165909038 | ||||||
| chr1:165909183 | C | T | 3 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0036 |
3 | HG02451.hp1 HG02451.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1360C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1360 | chr1 | 165909183 | ||||||
| chr1:165909261 | C | T | 4 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(1): Show |
46 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1438C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1438 | chr1 | 165909261 | ||||||
| chr1:165909389 | C | G | 1 | a0001c0002t0015 | 2 | NA18941.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1566C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1566 | chr1 | 165909389 | ||||||
| chr1:165909477 | G | T | 1 | a0001c0002t0020 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1654G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1654 | chr1 | 165909477 | ||||||
| chr1:165909541 | T | C | 1 | a0001c0001t0027 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1718 | chr1 | 165909541 | ||||||
| chr1:165909566 | C | T | 1 | a0001c0001t0026 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1743 | chr1 | 165909566 | ||||||
| chr1:165909674 | C | T | 4 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0022 others(1): Show |
26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1851C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1851 | chr1 | 165909674 | ||||||
| chr1:165909766 | A | G | 1 | a0001c0001t0008 | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1943A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1943 | chr1 | 165909766 | ||||||
| chr1:165910021 | C | G | 1 | a0001c0001t0014 | 3 | NA19062.hp1 NA19086.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2198C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2198 | chr1 | 165910021 | ||||||
| chr1:165910042 | T | G | 1 | a0001c0001t0008 | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2219T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2219 | chr1 | 165910042 | ||||||
| chr1:165910385 | A | C | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(8): Show |
78 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2562A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2562 | chr1 | 165910385 | ||||||
| chr1:165910495 | C | T | 1 | a0001c0001t0023 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2672C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2672 | chr1 | 165910495 | ||||||
| chr1:165910500 | G | A | 1 | a0001c0001t0021 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2677G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2677 | chr1 | 165910500 | ||||||
| chr1:165910584 | A | G | 1 | a0001c0001t0033 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2761 | chr1 | 165910584 | ||||||
| chr1:165910608 | G | A | 1 | a0001c0001t0028 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2785G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2785 | chr1 | 165910608 | ||||||
| chr1:165910654 | A | G | 1 | a0001c0001t0008 | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2831A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2831 | chr1 | 165910654 | ||||||
| chr1:165910794 | A | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*2971A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2971 | chr1 | 165910794 | ||||||
| chr1:165910874 | T | A | 1 | a0001c0001t0016 | 2 | HG03195.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3051T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3051 | chr1 | 165910874 | ||||||
| chr1:165910874 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*3051T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3051 | chr1 | 165910874 | ||||||
| chr1:165910957 | G | A | 1 | a0001c0001t0013 | 3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3134G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3134 | chr1 | 165910957 | ||||||
| chr1:165911084 | C | G | 3 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0036 |
3 | HG02451.hp1 HG02451.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3261C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3261 | chr1 | 165911084 | ||||||
| chr1:165911193 | A | G | 3 | a0001c0001t0009 a0001c0001t0017 a0002c0003t0009 |
11 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3370A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3370 | chr1 | 165911193 | ||||||
| chr1:165911377 | C | G | 1 | a0001c0001t0022 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3554C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3554 | chr1 | 165911377 | ||||||
| chr1:165911465 | T | C | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3642T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3642 | chr1 | 165911465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:165828075 | G | C | 2 | a0001c0001t0005g0005 a0001c0001t0005g0006 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.99+143G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828075 | |||||||
| chr1:165828076 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0004g0009 |
3 | HG01978.hp1 NA18944.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.99+144T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828076 | |||||||
| chr1:165828081 | C | G | 1 | a0001c0001t0013g0315 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99+149C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828081 | |||||||
| chr1:165828103 | C | CG | 11 | a0001c0001t0001g0304 a0001c0001t0001g0310 a0001c0001t0001g0312 others(8): Show |
11 | HG01978.hp2 HG02129.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+173dupG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165828103 | ||||||
| chr1:165828112 | C | T | 40 | a0001c0001t0001g0289 a0001c0001t0001g0299 a0001c0001t0001g0304 others(37): Show |
41 | HG01978.hp2 HG02055.hp1 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.99+180C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828112 | |||||||
| chr1:165828312 | C | T | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+380C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828312 | |||||||
| chr1:165828619 | T | C | 18 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0011 others(15): Show |
19 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+687T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828619 | |||||||
| chr1:165828729 | C | A | 299 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(296): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.99+797C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828729 | |||||||
| chr1:165828774 | G | T | 101 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0165 others(98): Show |
101 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.99+842G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828774 | |||||||
| chr1:165829089 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.99+1157T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829089 | |||||||
| chr1:165829160 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.99+1228T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829160 | |||||||
| chr1:165829163 | T | C | 4 | a0001c0001t0004g0011 a0001c0001t0012g0012 a0001c0001t0025g0275 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1231T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829163 | |||||||
| chr1:165829406 | G | A | 1 | a0001c0001t0009g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+1474G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829406 | |||||||
| chr1:165829480 | G | T | 1 | a0001c0001t0010g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.99+1548G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829480 | |||||||
| chr1:165829596 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.99+1664C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829596 | |||||||
| chr1:165829643 | G | C | 1 | a0001c0001t0009g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+1711G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829643 | |||||||
| chr1:165829785 | G | A | 94 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0025 others(91): Show |
98 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.99+1853G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829785 | |||||||
| chr1:165829903 | A | G | 25 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(22): Show |
25 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+1971A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829903 | |||||||
| chr1:165830046 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+2114C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830046 | |||||||
| chr1:165830207 | G | C | 13 | a0001c0001t0001g0299 a0001c0001t0002g0294 a0001c0001t0004g0291 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+2275G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830207 | |||||||
| chr1:165830216 | C | T | 15 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(12): Show |
16 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+2284C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830216 | |||||||
| chr1:165830239 | A | G | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+2307A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830239 | |||||||
| chr1:165830318 | A | T | 5 | a0001c0001t0004g0011 a0001c0001t0012g0012 a0001c0001t0025g0275 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2386A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830318 | |||||||
| chr1:165830330 | AT | A | 253 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(250): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.99+2410delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165830330 | ||||||
| chr1:165830333 | T | A | 4 | a0001c0001t0004g0011 a0001c0001t0032g0259 a0001c0001t0033g0010 others(1): Show |
4 | HG01515.hp1 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2401T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830333 | |||||||
| chr1:165830417 | C | T | 1 | a0001c0001t0003g0257 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.99+2485C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830417 | |||||||
| chr1:165830482 | G | T | 94 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0025 others(91): Show |
98 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.99+2550G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830482 | |||||||
| chr1:165830566 | C | T | 1 | a0001c0001t0004g0303 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+2634C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830566 | |||||||
| chr1:165830571 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0009g0288 |
2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.99+2639C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830571 | |||||||
| chr1:165830615 | A | G | 240 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(237): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.99+2683A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830615 | |||||||
| chr1:165830617 | G | GC | 121 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0165 others(118): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.99+2687dupC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165830617 | ||||||
| chr1:165830619 | C | T | 1 | a0001c0001t0009g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+2687C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830619 | |||||||
| chr1:165830701 | A | G | 13 | a0001c0001t0001g0299 a0001c0001t0002g0294 a0001c0001t0004g0291 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+2769A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830701 | |||||||
| chr1:165830756 | G | A | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+2824G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830756 | |||||||
| chr1:165830772 | A | G | 146 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0165 others(143): Show |
147 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.99+2840A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830772 | |||||||
| chr1:165830819 | A | C | 2 | a0001c0001t0001g0100 a0001c0002t0005g0101 |
2 | HG01175.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.99+2887A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830819 | |||||||
| chr1:165830823 | C | T | 1 | a0001c0001t0004g0256 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.99+2891C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830823 | |||||||
| chr1:165831038 | G | A | 15 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(12): Show |
16 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+3106G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831038 | |||||||
| chr1:165831040 | C | T | 3 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 |
3 | HG01884.hp1 HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+3108C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831040 | |||||||
| chr1:165831217 | A | G | 2 | a0001c0001t0001g0098 a0001c0002t0005g0099 |
2 | HG02080.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.99+3285A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831217 | |||||||
| chr1:165831228 | G | A | 1 | a0001c0001t0004g0291 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+3296G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831228 | |||||||
| chr1:165831453 | A | G | 15 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(12): Show |
16 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+3521A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831453 | |||||||
| chr1:165831534 | G | T | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+3602G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831534 | |||||||
| chr1:165831541 | G | A | 1 | a0001c0001t0009g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+3609G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831541 | |||||||
| chr1:165831545 | T | C | 1 | a0001c0001t0004g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99+3613T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831545 | |||||||
| chr1:165831584 | C | T | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+3652C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831584 | |||||||
| chr1:165831677 | A | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0165 others(128): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.99+3745A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831677 | |||||||
| chr1:165831873 | C | A | 1 | a0001c0001t0008g0016 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.99+3941C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831873 | |||||||
| chr1:165831989 | G | A | 1 | a0001c0001t0012g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+4057G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831989 | |||||||
| chr1:165832013 | C | A | 10 | a0001c0001t0002g0279 a0001c0001t0004g0282 a0001c0001t0004g0284 others(7): Show |
10 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+4081C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832013 | |||||||
| chr1:165832084 | G | T | 10 | a0001c0001t0002g0279 a0001c0001t0004g0282 a0001c0001t0004g0284 others(7): Show |
10 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+4152G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832084 | |||||||
| chr1:165832397 | A | G | 18 | a0001c0001t0001g0299 a0001c0001t0002g0294 a0001c0001t0004g0011 others(15): Show |
18 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+4465A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832397 | |||||||
| chr1:165832488 | T | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0025 others(34): Show |
39 | HG00140.hp2 HG00733.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.99+4556T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832488 | |||||||
| chr1:165832516 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0006g0049 |
3 | HG02257.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.99+4584G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832516 | |||||||
| chr1:165832570 | T | C | 15 | a0001c0001t0001g0299 a0001c0001t0002g0294 a0001c0001t0003g0122 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+4638T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832570 | |||||||
| chr1:165832889 | T | G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99+4957T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832889 | |||||||
| chr1:165832946 | C | T | 3 | a0001c0001t0004g0011 a0001c0001t0012g0012 a0001c0001t0033g0010 |
3 | HG02145.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.99+5014C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832946 | |||||||
| chr1:165832947 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG00639.hp2 HG01358.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+5015G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832947 | |||||||
| chr1:165833089 | T | C | 33 | a0001c0001t0001g0289 a0001c0001t0002g0108 a0001c0001t0002g0109 others(30): Show |
34 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.99+5157T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833089 | |||||||
| chr1:165833145 | C | G | 19 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0114 others(16): Show |
19 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+5213C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833145 | |||||||
| chr1:165833191 | C | G | 13 | a0001c0001t0001g0304 a0001c0001t0001g0310 a0001c0001t0001g0312 others(10): Show |
13 | HG01192.hp2 HG01978.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+5259C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833191 | |||||||
| chr1:165833233 | G | A | 14 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(11): Show |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5301G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833233 | |||||||
| chr1:165833361 | C | G | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG01978.hp2 HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.99+5429C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833361 | |||||||
| chr1:165833438 | T | C | 14 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(11): Show |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5506T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833438 | |||||||
| chr1:165833480 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99+5548C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833480 | |||||||
| chr1:165833531 | C | T | 1 | a0001c0001t0008g0255 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.99+5599C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833531 | |||||||
| chr1:165833613 | T | G | 1 | a0001c0001t0003g0164 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99+5681T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833613 | |||||||
| chr1:165833709 | A | G | 14 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(11): Show |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5777A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833709 | |||||||
| chr1:165833794 | G | A | 14 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(11): Show |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5862G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833794 | |||||||
| chr1:165833926 | A | G | 5 | a0001c0001t0002g0133 a0001c0001t0013g0134 a0001c0001t0013g0315 others(2): Show |
5 | HG02258.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5994A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833926 | |||||||
| chr1:165833931 | T | C | 14 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(11): Show |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5999T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833931 | |||||||
| chr1:165834023 | T | A | 15 | a0001c0001t0001g0299 a0001c0001t0002g0294 a0001c0001t0003g0122 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+6091T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834023 | |||||||
| chr1:165834175 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.99+6243G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834175 | |||||||
| chr1:165834414 | T | G | 32 | a0001c0001t0001g0299 a0001c0001t0001g0304 a0001c0001t0001g0310 others(29): Show |
32 | HG01192.hp2 HG01978.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+6482T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834414 | |||||||
| chr1:165834580 | G | T | 20 | a0001c0001t0001g0299 a0001c0001t0002g0294 a0001c0001t0003g0122 others(17): Show |
20 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+6648G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834580 | |||||||
| chr1:165834681 | T | A | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+6749T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834681 | |||||||
| chr1:165834713 | C | T | 12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6781C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834713 | |||||||
| chr1:165834757 | G | A | 1 | a0001c0001t0029g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+6825G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834757 | |||||||
| chr1:165834818 | C | T | 1 | a0001c0001t0004g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+6886C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834818 | |||||||
| chr1:165834896 | G | A | 12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6964G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834896 | |||||||
| chr1:165834993 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.99+7061C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834993 | |||||||
| chr1:165835006 | CT | C | 12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+7082delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835006 | ||||||
| chr1:165835060 | A | G | 3 | a0001c0001t0004g0011 a0001c0001t0012g0012 a0001c0001t0033g0010 |
3 | HG02145.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.99+7128A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835060 | |||||||
| chr1:165835314 | T | TATATATA others(43): Show |
12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+7401_99+7402ins others(50): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835314 | ||||||
| chr1:165835359 | G | GTTA | 3 | a0001c0001t0006g0104 a0001c0001t0008g0166 a0001c0001t0036g0136 |
3 | HG02451.hp1 NA18522.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.99+7448_99+7450dup others(3): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835359 | ||||||
| chr1:165835359 | GTTA | G | 12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+7448_99+7450del others(3): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835359 | ||||||
| chr1:165835505 | C | A | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+7573C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835505 | |||||||
| chr1:165835659 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+7727A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835659 | |||||||
| chr1:165835667 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+7735A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835667 | |||||||
| chr1:165835792 | A | G | 1 | a0001c0001t0011g0253 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.99+7860A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835792 | |||||||
| chr1:165836119 | T | G | 2 | a0001c0001t0001g0289 a0001c0001t0009g0288 |
2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.99+8187T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836119 | |||||||
| chr1:165836214 | G | T | 1 | a0001c0001t0012g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+8282G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836214 | |||||||
| chr1:165836222 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(211): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.99+8290C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836222 | |||||||
| chr1:165836223 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(211): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.99+8291C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836223 | |||||||
| chr1:165836233 | C | A | 12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8301C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836233 | |||||||
| chr1:165836240 | C | A | 12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8308C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836240 | |||||||
| chr1:165836245 | C | A | 12 | a0001c0001t0001g0289 a0001c0001t0002g0279 a0001c0001t0004g0282 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8313C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836245 | |||||||
| chr1:165836347 | T | G | 1 | a0001c0002t0005g0305 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.99+8415T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836347 | |||||||
| chr1:165836396 | T | A | 12 | a0001c0001t0001g0304 a0001c0001t0001g0310 a0001c0001t0001g0312 others(9): Show |
12 | HG01192.hp2 HG01978.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8464T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836396 | |||||||
| chr1:165836405 | C | A | 4 | a0001c0001t0002g0017 a0001c0001t0014g0018 a0001c0001t0014g0019 others(1): Show |
4 | HG02027.hp2 NA19062.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+8473C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836405 | |||||||
| chr1:165836559 | C | T | 1 | a0001c0001t0010g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.99+8627C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836559 | |||||||
| chr1:165836595 | T | C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0056 a0001c0002t0005g0057 |
5 | HG01081.hp1 HG01099.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+8663T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836595 | |||||||
| chr1:165836600 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.99+8668A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836600 | |||||||
| chr1:165836688 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.99+8756G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836688 | |||||||
| chr1:165836757 | G | A | 1 | a0001c0001t0010g0170 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+8825G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836757 | |||||||
| chr1:165836800 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+8868T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836800 | |||||||
| chr1:165836873 | T | C | 3 | a0001c0001t0006g0167 a0001c0001t0006g0168 a0001c0001t0006g0277 |
3 | HG02486.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.99+8941T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836873 | |||||||
| chr1:165836941 | C | T | 1 | a0001c0001t0009g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+9009C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836941 | |||||||
| chr1:165837004 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.99+9072G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837004 | |||||||
| chr1:165837053 | A | C | 15 | a0001c0001t0001g0304 a0001c0001t0001g0310 a0001c0001t0001g0312 others(12): Show |
15 | HG01192.hp2 HG01978.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+9121A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837053 | |||||||
| chr1:165837152 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.99+9220T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837152 | |||||||
| chr1:165837240 | T | C | 1 | a0001c0001t0004g0059 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.99+9308T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837240 | |||||||
| chr1:165837315 | T | G | 1 | a0001c0001t0002g0017 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.99+9383T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837315 | |||||||
| chr1:165837847 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.99+9915C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837847 | |||||||
| chr1:165838575 | T | G | 24 | a0001c0001t0001g0052 a0001c0001t0001g0123 a0001c0001t0001g0124 others(21): Show |
24 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.99+10643T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838575 | |||||||
| chr1:165838610 | G | A | 2 | a0001c0001t0004g0118 a0001c0001t0033g0010 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.99+10678G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838610 | |||||||
| chr1:165838681 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.99+10749A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838681 | |||||||
| chr1:165838892 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99+10960A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838892 | |||||||
| chr1:165838966 | T | C | 1 | a0001c0001t0004g0175 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.99+11034T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838966 | |||||||
| chr1:165838979 | C | T | 140 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(137): Show |
142 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(139): Show |
intron_variant | MODIFIER | c.99+11047C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838979 | |||||||
| chr1:165839667 | G | A | 2 | a0001c0002t0005g0081 a0001c0002t0005g0082 |
2 | HG01256.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.99+11735G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839667 | |||||||
| chr1:165839738 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.99+11806G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839738 | |||||||
| chr1:165839750 | A | G | 156 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(153): Show |
158 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(155): Show |
intron_variant | MODIFIER | c.99+11818A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839750 | |||||||
| chr1:165839773 | T | C | 12 | a0001c0001t0002g0114 a0001c0001t0004g0112 a0001c0001t0004g0113 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+11841T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839773 | |||||||
| chr1:165839840 | C | T | 4 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0006g0283 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+11908C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839840 | |||||||
| chr1:165839851 | C | G | 133 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(130): Show |
135 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(132): Show |
intron_variant | MODIFIER | c.99+11919C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839851 | |||||||
| chr1:165839932 | C | T | 109 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(106): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+12000C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839932 | |||||||
| chr1:165839933 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+12001G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839933 | |||||||
| chr1:165839952 | G | A | 1 | a0001c0002t0005g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.99+12020G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839952 | |||||||
| chr1:165840023 | A | G | 1 | a0001c0001t0009g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+12091A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840023 | |||||||
| chr1:165840127 | C | G | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+12195C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840127 | |||||||
| chr1:165840164 | C | G | 2 | a0001c0001t0004g0284 a0001c0001t0006g0283 |
2 | HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.99+12232C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840164 | |||||||
| chr1:165840330 | A | G | 1 | a0001c0001t0009g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+12398A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840330 | |||||||
| chr1:165840353 | A | G | 193 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(190): Show |
195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.99+12421A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840353 | |||||||
| chr1:165840416 | A | G | 1 | a0001c0002t0015g0248 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.99+12484A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840416 | |||||||
| chr1:165840676 | G | A | 2 | a0001c0001t0003g0208 a0001c0001t0004g0256 |
2 | NA18992.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.99+12744G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840676 | |||||||
| chr1:165840693 | C | T | 12 | a0001c0001t0002g0114 a0001c0001t0004g0112 a0001c0001t0004g0113 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+12761C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840693 | |||||||
| chr1:165840926 | A | G | 73 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(70): Show |
75 | HG00673.hp2 HG01261.hp1 HG01943.hp2 others(72): Show |
intron_variant | MODIFIER | c.99+12994A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840926 | |||||||
| chr1:165841094 | C | T | 9 | a0001c0001t0002g0095 a0001c0001t0002g0273 a0001c0001t0002g0274 others(6): Show |
9 | HG01256.hp2 HG01258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+13162C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841094 | |||||||
| chr1:165841095 | G | T | 12 | a0001c0001t0002g0114 a0001c0001t0004g0112 a0001c0001t0004g0113 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+13163G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841095 | |||||||
| chr1:165841097 | A | ATG | 7 | a0001c0001t0002g0162 a0001c0001t0009g0062 a0001c0001t0009g0063 others(4): Show |
8 | HG02559.hp1 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+13179_99+13180d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841097 | ||||||
| chr1:165841097 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+13165A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841097 | |||||||
| chr1:165841109 | G | GTATATA | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0002g0263 others(5): Show |
8 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+13178_99+13179i others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841109 | ||||||
| chr1:165841109 | G | GTATATAT others(3): Show |
3 | a0001c0001t0009g0105 a0001c0001t0009g0276 a0001c0001t0028g0106 |
3 | HG02486.hp1 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.99+13178_99+13179i others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841109 | ||||||
| chr1:165841109 | GTGTA | G | 11 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0002g0139 others(8): Show |
11 | HG00673.hp1 HG01516.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+13179_99+13182d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841109 | ||||||
| chr1:165841111 | G | A | 13 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0002g0263 others(10): Show |
13 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+13179G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841111 | |||||||
| chr1:165841111 | G | GTA | 3 | a0001c0001t0002g0058 a0001c0001t0004g0061 a0001c0001t0007g0140 |
3 | HG01496.hp1 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.99+13200_99+13201d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | ||||||
| chr1:165841111 | G | GTATA | 8 | a0001c0001t0001g0052 a0001c0001t0001g0172 a0001c0001t0001g0266 others(5): Show |
8 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+13198_99+13201d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | ||||||
| chr1:165841111 | G | GTGTA | 11 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0279 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+13180_99+13181i others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | ||||||
| chr1:165841111 | GTA | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+13200_99+13201d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | ||||||
| chr1:165841111 | GTATA | G | 134 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(131): Show |
136 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(133): Show |
intron_variant | MODIFIER | c.99+13198_99+13201d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | ||||||
| chr1:165841111 | GTATATA | G | 3 | a0001c0001t0002g0241 a0001c0001t0010g0252 a0001c0001t0026g0240 |
3 | HG02132.hp1 NA18964.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.99+13196_99+13201d others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | ||||||
| chr1:165841113 | A | G | 5 | a0001c0001t0002g0160 a0001c0001t0004g0282 a0001c0001t0004g0284 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+13181A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841113 | |||||||
| chr1:165841115 | A | G | 113 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(110): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.99+13183A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841115 | |||||||
| chr1:165841117 | A | G | 1 | a0001c0001t0004g0009 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.99+13185A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841117 | |||||||
| chr1:165841407 | C | T | 3 | a0001c0001t0009g0105 a0001c0001t0025g0275 a0001c0001t0028g0106 |
3 | HG02486.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99+13475C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841407 | |||||||
| chr1:165841433 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+13501A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841433 | |||||||
| chr1:165841454 | G | C | 1 | a0001c0001t0008g0255 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.99+13522G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841454 | |||||||
| chr1:165841497 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.99+13565T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841497 | |||||||
| chr1:165841572 | C | T | 1 | a0001c0001t0006g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+13640C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841572 | |||||||
| chr1:165841673 | C | G | 2 | a0001c0001t0004g0011 a0001c0001t0004g0303 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+13741C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841673 | |||||||
| chr1:165841815 | T | G | 171 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(168): Show |
174 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(171): Show |
intron_variant | MODIFIER | c.99+13883T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841815 | |||||||
| chr1:165841824 | G | A | 2 | a0001c0001t0004g0118 a0001c0001t0033g0010 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.99+13892G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841824 | |||||||
| chr1:165841856 | C | T | 2 | a0001c0001t0010g0093 a0001c0001t0010g0247 |
2 | HG02135.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.99+13924C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841856 | |||||||
| chr1:165842176 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.99+14244C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842176 | |||||||
| chr1:165842249 | C | A | 154 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(151): Show |
156 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(153): Show |
intron_variant | MODIFIER | c.99+14317C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842249 | |||||||
| chr1:165842447 | A | G | 15 | a0001c0001t0001g0052 a0001c0001t0001g0123 a0001c0001t0001g0124 others(12): Show |
15 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+14515A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842447 | |||||||
| chr1:165842464 | T | C | 1 | a0001c0001t0003g0209 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.99+14532T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842464 | |||||||
| chr1:165842492 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+14560C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842492 | |||||||
| chr1:165842505 | G | A | 3 | a0001c0001t0002g0162 a0001c0001t0012g0012 a0001c0001t0017g0004 |
4 | HG02976.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+14573G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842505 | |||||||
| chr1:165842705 | C | G | 1 | a0001c0001t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+14773C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842705 | |||||||
| chr1:165842848 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+14916C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842848 | |||||||
| chr1:165842870 | A | G | 2 | a0001c0001t0003g0158 a0001c0001t0003g0159 |
2 | HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.99+14938A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842870 | |||||||
| chr1:165842883 | A | C | 155 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(152): Show |
157 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(154): Show |
intron_variant | MODIFIER | c.99+14951A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842883 | |||||||
| chr1:165842932 | C | G | 6 | a0001c0001t0002g0139 a0001c0001t0002g0161 a0001c0001t0002g0174 others(3): Show |
6 | HG00673.hp1 HG01516.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+15000C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842932 | |||||||
| chr1:165843047 | G | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0094 a0001c0001t0004g0302 |
3 | HG02280.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+15115G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843047 | |||||||
| chr1:165843090 | TTC | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+15160_99+15161d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165843090 | ||||||
| chr1:165843457 | A | C | 1 | a0001c0001t0009g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+15525A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843457 | |||||||
| chr1:165843562 | G | A | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+15630G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843562 | |||||||
| chr1:165843769 | C | T | 172 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(169): Show |
174 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.99+15837C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843769 | |||||||
| chr1:165843802 | A | G | 1 | a0001c0002t0005g0082 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99+15870A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843802 | |||||||
| chr1:165843884 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0007g0264 |
2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.99+15952A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843884 | |||||||
| chr1:165843941 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0002g0003 a0001c0001t0002g0036 others(1): Show |
5 | HG01261.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+16009A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843941 | |||||||
| chr1:165844008 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.99+16076G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844008 | |||||||
| chr1:165844171 | G | A | 2 | a0001c0001t0004g0011 a0001c0001t0004g0303 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+16239G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844171 | |||||||
| chr1:165844173 | C | A | 2 | a0001c0001t0009g0105 a0001c0001t0028g0106 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+16241C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844173 | |||||||
| chr1:165844271 | G | A | 307 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(304): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.99+16339G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844271 | |||||||
| chr1:165844279 | C | T | 1 | a0001c0002t0015g0248 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.99+16347C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844279 | |||||||
| chr1:165844280 | A | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0006g0049 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+16348A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844280 | |||||||
| chr1:165844483 | C | G | 143 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(140): Show |
145 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(142): Show |
intron_variant | MODIFIER | c.99+16551C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844483 | |||||||
| chr1:165844523 | T | G | 1 | a0001c0001t0002g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+16591T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844523 | |||||||
| chr1:165844625 | G | A | 133 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.99+16693G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844625 | |||||||
| chr1:165844783 | TTGAA | T | 4 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0006g0283 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+16855_99+16858d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165844783 | ||||||
| chr1:165844807 | A | G | 1 | a0001c0001t0003g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.99+16875A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844807 | |||||||
| chr1:165844844 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.99+16912G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844844 | |||||||
| chr1:165844864 | T | G | 19 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0162 others(16): Show |
20 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+16932T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844864 | |||||||
| chr1:165844965 | C | T | 6 | a0001c0001t0001g0299 a0001c0001t0004g0065 a0001c0001t0004g0148 others(3): Show |
6 | HG01243.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+17033C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844965 | |||||||
| chr1:165845041 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.99+17109C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845041 | |||||||
| chr1:165845332 | C | T | 2 | a0001c0001t0004g0011 a0001c0001t0004g0303 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+17400C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845332 | |||||||
| chr1:165845468 | T | G | 2 | a0001c0001t0001g0182 a0001c0002t0005g0183 |
2 | HG02523.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.99+17536T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845468 | |||||||
| chr1:165845510 | C | T | 1 | a0002c0003t0009g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.99+17578C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845510 | |||||||
| chr1:165845926 | G | A | 1 | a0001c0001t0008g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.99+17994G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845926 | |||||||
| chr1:165846075 | T | G | 2 | a0001c0001t0004g0262 a0001c0001t0010g0261 |
2 | NA18984.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+18143T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846075 | |||||||
| chr1:165846446 | T | TAAACA | 8 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0006g0283 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+18535_99+18539d others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165846446 | ||||||
| chr1:165846446 | TAAACA | T | 13 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0002g0092 others(10): Show |
13 | HG00673.hp1 HG00735.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+18535_99+18539d others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165846446 | ||||||
| chr1:165846446 | TAAACAAA others(3): Show |
T | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+18530_99+18539d others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165846446 | ||||||
| chr1:165846597 | A | G | 1 | a0001c0001t0029g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+18665A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846597 | |||||||
| chr1:165846702 | T | C | 165 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(162): Show |
168 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+18770T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846702 | |||||||
| chr1:165846710 | G | C | 1 | a0001c0001t0002g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99+18778G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846710 | |||||||
| chr1:165846946 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.99+19014T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846946 | |||||||
| chr1:165847000 | G | A | 1 | a0001c0001t0033g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+19068G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847000 | |||||||
| chr1:165847003 | T | C | 1 | a0001c0001t0016g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99+19071T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847003 | |||||||
| chr1:165847091 | C | T | 307 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(304): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.99+19159C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847091 | |||||||
| chr1:165847123 | A | T | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+19191A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847123 | |||||||
| chr1:165847136 | A | G | 1 | a0001c0001t0016g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99+19204A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847136 | |||||||
| chr1:165847238 | A | G | 1 | a0001c0001t0007g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+19306A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847238 | |||||||
| chr1:165847373 | G | GT | 3 | a0001c0001t0007g0064 a0001c0001t0007g0171 a0001c0002t0005g0269 |
3 | HG00323.hp1 HG01192.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.99+19442dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165847373 | ||||||
| chr1:165847452 | C | T | 5 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0006g0167 others(2): Show |
5 | HG01256.hp2 HG01258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+19520C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847452 | |||||||
| chr1:165847724 | C | T | 30 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0139 others(27): Show |
31 | HG00673.hp1 HG01516.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.99+19792C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847724 | |||||||
| chr1:165847858 | C | T | 2 | a0001c0001t0006g0278 a0001c0001t0007g0140 |
2 | HG01496.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.99+19926C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847858 | |||||||
| chr1:165848340 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+20408G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848340 | |||||||
| chr1:165848374 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.99+20442G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848374 | |||||||
| chr1:165848559 | C | CG | 11 | a0001c0001t0002g0114 a0001c0001t0004g0112 a0001c0001t0004g0113 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+20628dupG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165848559 | ||||||
| chr1:165848660 | C | A | 179 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(176): Show |
182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+20728C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848660 | |||||||
| chr1:165848662 | A | C | 179 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(176): Show |
182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+20730A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848662 | |||||||
| chr1:165848678 | C | A | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.99+20746C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848678 | |||||||
| chr1:165849020 | G | T | 3 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 |
3 | NA19062.hp1 NA19086.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.99+21088G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849020 | |||||||
| chr1:165849384 | G | A | 138 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(135): Show |
140 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(137): Show |
intron_variant | MODIFIER | c.99+21452G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849384 | |||||||
| chr1:165849653 | G | T | 2 | a0001c0001t0009g0105 a0001c0001t0028g0106 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+21721G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849653 | |||||||
| chr1:165849763 | C | T | 6 | a0001c0001t0001g0299 a0001c0001t0004g0065 a0001c0001t0004g0148 others(3): Show |
6 | HG01243.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+21831C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849763 | |||||||
| chr1:165849911 | C | T | 2 | a0001c0001t0009g0105 a0001c0001t0028g0106 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+21979C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849911 | |||||||
| chr1:165850010 | A | G | 43 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0089 others(40): Show |
45 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.99+22078A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850010 | |||||||
| chr1:165850221 | C | T | 5 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0001t0007g0157 others(2): Show |
5 | HG01109.hp2 HG01256.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+22289C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850221 | |||||||
| chr1:165850233 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.99+22301C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850233 | |||||||
| chr1:165850292 | G | A | 1 | a0001c0001t0002g0212 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.99+22360G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850292 | |||||||
| chr1:165850420 | G | A | 179 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(176): Show |
182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+22488G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850420 | |||||||
| chr1:165850602 | C | T | 11 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0002g0092 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+22670C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850602 | |||||||
| chr1:165850616 | AT | A | 185 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0050 others(182): Show |
188 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.99+22704delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850616 | ||||||
| chr1:165850616 | ATT | A | 101 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.99+22703_99+22704d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850616 | ||||||
| chr1:165850616 | ATTT | A | 21 | a0001c0001t0001g0027 a0001c0001t0001g0142 a0001c0001t0001g0143 others(18): Show |
21 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+22702_99+22704d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850616 | ||||||
| chr1:165850711 | C | T | 2 | a0001c0001t0007g0090 a0001c0001t0007g0091 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.99+22779C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850711 | |||||||
| chr1:165850743 | C | T | 116 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(113): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.99+22811C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850743 | |||||||
| chr1:165850813 | G | A | 5 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0006g0167 others(2): Show |
5 | HG01256.hp2 HG01258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+22881G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850813 | |||||||
| chr1:165850927 | AT | A | 8 | a0001c0001t0004g0061 a0001c0001t0004g0112 a0001c0001t0006g0278 others(5): Show |
8 | HG01496.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+23022delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | ||||||
| chr1:165850927 | ATTT | A | 20 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0162 others(17): Show |
21 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+23020_99+23022d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | ||||||
| chr1:165850927 | ATTTTT | A | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(111): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.99+23018_99+23022d others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | ||||||
| chr1:165850927 | ATTTTTT | A | 6 | a0001c0001t0001g0185 a0001c0001t0002g0176 a0001c0001t0002g0263 others(3): Show |
6 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+23017_99+23022d others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | ||||||
| chr1:165850927 | ATTTTTTT others(1): Show |
A | 8 | a0001c0001t0002g0211 a0001c0001t0006g0111 a0001c0001t0006g0119 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+23015_99+23022d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | ||||||
| chr1:165850927 | ATTTTTTT others(5): Show |
A | 13 | a0001c0001t0002g0139 a0001c0001t0002g0161 a0001c0001t0002g0174 others(10): Show |
13 | HG00673.hp1 HG01516.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+23011_99+23022d others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | ||||||
| chr1:165850940 | T | A | 1 | a0001c0001t0009g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+23008T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850940 | |||||||
| chr1:165850954 | T | A | 15 | a0001c0001t0002g0114 a0001c0001t0002g0211 a0001c0001t0003g0039 others(12): Show |
15 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+23022T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850954 | |||||||
| chr1:165850954 | T | TA | 9 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0003g0087 others(6): Show |
9 | HG01257.hp2 HG03041.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+23024dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850954 | ||||||
| chr1:165850954 | T | TTA | 97 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(94): Show |
99 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.99+23022_99+23023i others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850954 | |||||||
| chr1:165850954 | T | TTTA | 19 | a0001c0001t0001g0086 a0001c0001t0001g0233 a0001c0001t0001g0234 others(16): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+23022_99+23023i others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850954 | |||||||
| chr1:165850977 | GTTGCTTG others(3): Show |
G | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+23047_99+23056d others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850977 | ||||||
| chr1:165851137 | C | T | 6 | a0001c0001t0001g0299 a0001c0001t0004g0065 a0001c0001t0004g0148 others(3): Show |
6 | HG01243.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+23205C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851137 | |||||||
| chr1:165851146 | T | C | 20 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0162 others(17): Show |
21 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+23214T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851146 | |||||||
| chr1:165851176 | A | C | 20 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0162 others(17): Show |
21 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+23244A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851176 | |||||||
| chr1:165851251 | A | G | 1 | a0001c0002t0005g0305 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.99+23319A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851251 | |||||||
| chr1:165851418 | C | T | 1 | a0001c0001t0010g0170 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+23486C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851418 | |||||||
| chr1:165851552 | A | G | 4 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0006g0283 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+23620A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851552 | |||||||
| chr1:165851588 | G | A | 1 | a0001c0001t0007g0271 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.99+23656G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851588 | |||||||
| chr1:165851692 | G | C | 138 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(135): Show |
140 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(137): Show |
intron_variant | MODIFIER | c.99+23760G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851692 | |||||||
| chr1:165851695 | T | C | 3 | a0001c0001t0009g0105 a0001c0001t0025g0275 a0001c0001t0028g0106 |
3 | HG02486.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99+23763T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851695 | |||||||
| chr1:165851794 | C | G | 10 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0002g0092 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+23862C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851794 | |||||||
| chr1:165851813 | A | G | 2 | a0001c0001t0004g0262 a0001c0001t0010g0261 |
2 | NA18984.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+23881A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851813 | |||||||
| chr1:165852040 | A | G | 1 | a0001c0001t0033g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+24108A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852040 | |||||||
| chr1:165852091 | G | A | 179 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(176): Show |
182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+24159G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852091 | |||||||
| chr1:165852193 | A | G | 1 | a0001c0001t0009g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+24261A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852193 | |||||||
| chr1:165852453 | A | C | 1 | a0001c0001t0008g0232 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.99+24521A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852453 | |||||||
| chr1:165852604 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.99+24672T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852604 | |||||||
| chr1:165852670 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0178 |
2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.99+24738A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852670 | |||||||
| chr1:165852726 | C | T | 2 | a0001c0001t0003g0230 a0001c0001t0031g0231 |
2 | NA18973.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.99+24794C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852726 | |||||||
| chr1:165852775 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99+24843G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852775 | |||||||
| chr1:165852939 | C | T | 137 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(134): Show |
139 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(136): Show |
intron_variant | MODIFIER | c.99+25007C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852939 | |||||||
| chr1:165853036 | A | G | 1 | a0001c0001t0009g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99+25104A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853036 | |||||||
| chr1:165853042 | GCCT | G | 13 | a0001c0001t0002g0139 a0001c0001t0002g0161 a0001c0001t0002g0174 others(10): Show |
13 | HG00673.hp1 HG01516.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+25111_99+25113d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853042 | |||||||
| chr1:165853356 | AT | A | 22 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(19): Show |
22 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.99+25435delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165853356 | ||||||
| chr1:165853358 | T | A | 135 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(132): Show |
137 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(134): Show |
intron_variant | MODIFIER | c.99+25426T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853358 | |||||||
| chr1:165853491 | C | G | 1 | a0001c0002t0005g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99+25559C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853491 | |||||||
| chr1:165853503 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0002g0092 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+25571G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853503 | |||||||
| chr1:165853535 | C | T | 1 | a0001c0002t0005g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99+25603C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853535 | |||||||
| chr1:165853654 | T | C | 132 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.99+25722T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853654 | |||||||
| chr1:165853803 | T | C | 167 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(164): Show |
170 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(167): Show |
intron_variant | MODIFIER | c.99+25871T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853803 | |||||||
| chr1:165854496 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+26564C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854496 | |||||||
| chr1:165854556 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.99+26624C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854556 | |||||||
| chr1:165854598 | A | AAAAT | 45 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0031 others(42): Show |
46 | HG01261.hp1 HG01515.hp1 HG01943.hp2 others(43): Show |
intron_variant | MODIFIER | c.99+26710_99+26713d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | ||||||
| chr1:165854598 | A | AAAATAAA others(1): Show |
6 | a0001c0001t0001g0097 a0001c0001t0001g0200 a0001c0001t0001g0202 others(3): Show |
6 | HG02027.hp1 HG02735.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+26706_99+26713d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | ||||||
| chr1:165854598 | AAAAT | A | 154 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0045 others(151): Show |
156 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.99+26710_99+26713d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | ||||||
| chr1:165854598 | AAAATAAA others(1): Show |
A | 10 | a0001c0001t0001g0149 a0001c0001t0002g0095 a0001c0001t0002g0139 others(7): Show |
10 | HG00673.hp1 HG00735.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+26706_99+26713d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | ||||||
| chr1:165854598 | AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+26702_99+26713d others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | ||||||
| chr1:165854598 | AAAATAAA others(13): Show |
A | 1 | a0001c0001t0006g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+26694_99+26713d others(22): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | ||||||
| chr1:165854824 | A | G | 1 | a0001c0001t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+26892A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854824 | |||||||
| chr1:165854881 | C | G | 3 | a0001c0001t0004g0154 a0001c0001t0004g0155 a0001c0001t0011g0040 |
3 | NA19005.hp1 NA19057.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.99+26949C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854881 | |||||||
| chr1:165855107 | A | G | 4 | a0001c0001t0006g0104 a0001c0001t0006g0115 a0001c0001t0006g0116 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+27175A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855107 | |||||||
| chr1:165855169 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.99+27237A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855169 | |||||||
| chr1:165855254 | T | C | 1 | a0001c0002t0005g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.99+27322T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855254 | |||||||
| chr1:165855510 | C | CT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0124 a0001c0001t0001g0172 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+27596dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165855510 | ||||||
| chr1:165855510 | CT | C | 7 | a0001c0001t0001g0237 a0001c0001t0004g0059 a0001c0001t0004g0112 others(4): Show |
7 | HG02647.hp2 HG02976.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+27596delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165855510 | ||||||
| chr1:165855666 | G | A | 10 | a0001c0001t0002g0114 a0001c0001t0004g0112 a0001c0001t0004g0113 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+27734G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855666 | |||||||
| chr1:165855682 | C | T | 2 | a0001c0001t0009g0105 a0001c0001t0028g0106 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+27750C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855682 | |||||||
| chr1:165855741 | C | T | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+27809C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855741 | |||||||
| chr1:165855896 | A | G | 97 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0130 others(94): Show |
97 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.99+27964A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855896 | |||||||
| chr1:165855907 | G | A | 1 | a0001c0001t0033g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+27975G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855907 | |||||||
| chr1:165855929 | G | A | 204 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(201): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.99+27997G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855929 | |||||||
| chr1:165856050 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+28118A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856050 | |||||||
| chr1:165856062 | C | T | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+28130C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856062 | |||||||
| chr1:165856157 | A | G | 1 | a0001c0002t0005g0183 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.99+28225A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856157 | |||||||
| chr1:165856230 | G | A | 23 | a0001c0001t0001g0052 a0001c0001t0001g0123 a0001c0001t0001g0124 others(20): Show |
23 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+28298G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856230 | |||||||
| chr1:165856285 | G | T | 5 | a0001c0001t0001g0038 a0001c0001t0002g0003 a0001c0001t0002g0036 others(2): Show |
6 | HG01261.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+28353G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856285 | |||||||
| chr1:165856329 | GTCTGATA others(974): Show |
G | 1 | a0001c0001t0033g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+28428_99+29408d others(2): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856329 | ||||||
| chr1:165856350 | A | T | 2 | a0001c0001t0003g0230 a0001c0001t0031g0231 |
2 | NA18973.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.99+28418A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856350 | |||||||
| chr1:165856354 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.99+28422A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856354 | |||||||
| chr1:165856361 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+28429C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856361 | |||||||
| chr1:165856406 | A | AT | 87 | a0001c0001t0001g0021 a0001c0001t0001g0074 a0001c0001t0001g0143 others(84): Show |
90 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.99+28488dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856406 | ||||||
| chr1:165856406 | AT | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0111 a0001c0001t0006g0119 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+28488delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856406 | ||||||
| chr1:165856420 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.99+28488T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856420 | |||||||
| chr1:165856447 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+28515C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856447 | |||||||
| chr1:165856497 | C | A | 8 | a0001c0001t0004g0011 a0001c0001t0004g0118 a0001c0001t0004g0303 others(5): Show |
8 | HG02145.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+28565C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856497 | |||||||
| chr1:165856752 | G | A | 22 | a0001c0001t0001g0045 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG00735.hp2 HG01243.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.99+28820G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856752 | |||||||
| chr1:165856901 | G | GTT | 9 | a0001c0001t0002g0003 a0001c0001t0002g0036 a0001c0001t0003g0204 others(6): Show |
10 | HG00673.hp2 HG01261.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+28987_99+28988d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856901 | ||||||
| chr1:165856901 | GT | G | 187 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(184): Show |
188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.99+28988delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856901 | ||||||
| chr1:165856907 | T | G | 64 | a0001c0001t0001g0042 a0001c0001t0001g0097 a0001c0001t0001g0177 others(61): Show |
66 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.99+28975T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856907 | |||||||
| chr1:165856955 | G | A | 1 | a0001c0001t0008g0232 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.99+29023G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856955 | |||||||
| chr1:165856957 | AG | A | 84 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.99+29027delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856957 | ||||||
| chr1:165857012 | G | A | 1 | a0001c0001t0006g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+29080G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857012 | |||||||
| chr1:165857069 | C | G | 30 | a0001c0001t0001g0299 a0001c0001t0002g0095 a0001c0001t0002g0109 others(27): Show |
30 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.99+29137C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857069 | |||||||
| chr1:165857131 | C | T | 4 | a0001c0001t0010g0093 a0001c0001t0010g0170 a0001c0001t0010g0247 others(1): Show |
4 | HG02135.hp1 NA18979.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+29199C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857131 | |||||||
| chr1:165857292 | C | T | 1 | a0001c0001t0012g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+29360C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857292 | |||||||
| chr1:165857498 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+29566G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857498 | |||||||
| chr1:165857508 | G | A | 262 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.99+29576G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857508 | |||||||
| chr1:165857653 | C | A | 3 | a0001c0001t0008g0030 a0001c0001t0008g0071 a0001c0001t0008g0072 |
3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.99+29721C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857653 | |||||||
| chr1:165857665 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.99+29733A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857665 | |||||||
| chr1:165857784 | C | A | 2 | a0001c0001t0016g0066 a0001c0001t0016g0286 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.99+29852C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857784 | |||||||
| chr1:165857889 | T | C | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+29957T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857889 | |||||||
| chr1:165858145 | T | C | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+30213T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858145 | |||||||
| chr1:165858186 | A | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0009g0014 others(3): Show |
7 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+30254A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858186 | |||||||
| chr1:165858251 | G | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0043 others(46): Show |
51 | HG00099.hp2 HG00323.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.99+30319G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858251 | |||||||
| chr1:165858257 | G | T | 11 | a0001c0001t0004g0011 a0001c0001t0004g0118 a0001c0001t0004g0303 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+30325G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858257 | |||||||
| chr1:165858452 | C | T | 1 | a0001c0002t0005g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99+30520C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858452 | |||||||
| chr1:165858453 | G | A | 2 | a0001c0001t0006g0049 a0001c0001t0033g0010 |
2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.99+30521G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858453 | |||||||
| chr1:165858504 | G | A | 1 | a0001c0001t0007g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.99+30572G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858504 | |||||||
| chr1:165858671 | AG | A | 17 | a0001c0001t0001g0299 a0001c0001t0004g0059 a0001c0001t0004g0065 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+30741delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165858671 | ||||||
| chr1:165858745 | A | G | 1 | a0001c0001t0003g0034 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.99+30813A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858745 | |||||||
| chr1:165858894 | T | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(5): Show |
8 | HG02258.hp1 HG02451.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+30962T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858894 | |||||||
| chr1:165859078 | G | A | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-31126G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859078 | |||||||
| chr1:165859085 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-31119C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859085 | |||||||
| chr1:165859178 | AGTGG | A | 35 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0299 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-31018_100-3101 others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165859178 | ||||||
| chr1:165859257 | T | TA | 11 | a0001c0001t0004g0011 a0001c0001t0004g0118 a0001c0001t0004g0303 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-30946dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165859257 | ||||||
| chr1:165859301 | C | T | 3 | a0001c0001t0009g0105 a0001c0001t0017g0004 a0002c0003t0009g0080 |
4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-30903C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859301 | |||||||
| chr1:165859307 | G | A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0036 a0001c0001t0002g0095 others(11): Show |
15 | HG00673.hp2 HG01261.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-30897G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859307 | |||||||
| chr1:165859434 | G | A | 1 | a0001c0001t0010g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.100-30770G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859434 | |||||||
| chr1:165859566 | A | G | 1 | a0001c0001t0029g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.100-30638A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859566 | |||||||
| chr1:165859611 | C | T | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-30593C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859611 | |||||||
| chr1:165859652 | G | A | 17 | a0001c0001t0001g0299 a0001c0001t0004g0059 a0001c0001t0004g0065 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-30552G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859652 | |||||||
| chr1:165859919 | T | G | 101 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0100 others(98): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.100-30285T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859919 | |||||||
| chr1:165859964 | A | G | 2 | a0001c0001t0006g0049 a0001c0001t0033g0010 |
2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.100-30240A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859964 | |||||||
| chr1:165860041 | G | A | 1 | a0001c0002t0034g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.100-30163G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860041 | |||||||
| chr1:165860057 | A | G | 2 | a0001c0001t0003g0205 a0001c0001t0003g0206 |
2 | HG00673.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.100-30147A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860057 | |||||||
| chr1:165860060 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100-30144T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860060 | |||||||
| chr1:165860070 | G | A | 1 | a0001c0001t0008g0016 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.100-30134G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860070 | |||||||
| chr1:165860108 | C | T | 1 | a0002c0003t0009g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-30096C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860108 | |||||||
| chr1:165860495 | C | T | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-29709C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860495 | |||||||
| chr1:165860561 | A | C | 98 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(95): Show |
99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-29643A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860561 | |||||||
| chr1:165860720 | G | T | 20 | a0001c0001t0001g0299 a0001c0001t0003g0208 a0001c0001t0004g0059 others(17): Show |
20 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-29484G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860720 | |||||||
| chr1:165860726 | A | G | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-29478A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860726 | |||||||
| chr1:165860772 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-29432T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860772 | |||||||
| chr1:165860810 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100-29394A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860810 | |||||||
| chr1:165860937 | A | G | 3 | a0001c0001t0008g0030 a0001c0001t0008g0071 a0001c0001t0008g0072 |
3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100-29267A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860937 | |||||||
| chr1:165860947 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-29257G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860947 | |||||||
| chr1:165861079 | G | C | 97 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(94): Show |
98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.100-29125G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861079 | |||||||
| chr1:165861080 | G | A | 3 | a0001c0001t0006g0278 a0001c0001t0006g0292 a0001c0001t0007g0140 |
3 | HG01496.hp1 HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.100-29124G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861080 | |||||||
| chr1:165861247 | C | T | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG00673.hp2 HG02523.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-28957C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861247 | |||||||
| chr1:165861394 | C | T | 4 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0004g0137 others(1): Show |
4 | HG02451.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-28810C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861394 | |||||||
| chr1:165861403 | C | T | 98 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(95): Show |
99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-28801C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861403 | |||||||
| chr1:165861525 | A | G | 129 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(126): Show |
130 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.100-28679A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861525 | |||||||
| chr1:165861553 | A | G | 4 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0004g0137 others(1): Show |
4 | HG02451.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-28651A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861553 | |||||||
| chr1:165861576 | C | T | 1 | a0001c0002t0005g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.100-28628C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861576 | |||||||
| chr1:165861614 | C | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0152 a0001c0001t0001g0188 others(4): Show |
7 | HG00741.hp2 HG01255.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-28590C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861614 | |||||||
| chr1:165861615 | G | A | 98 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(95): Show |
99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-28589G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861615 | |||||||
| chr1:165861627 | C | CA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0026 others(31): Show |
34 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.100-28555dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861627 | ||||||
| chr1:165861627 | C | CAA | 8 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0130 others(5): Show |
8 | HG01106.hp1 HG01109.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-28556_100-2855 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861627 | ||||||
| chr1:165861634 | AAAAAAAA others(9): Show |
A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | NA18985.hp1 NA18992.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-28560_100-2854 others(20): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861634 | ||||||
| chr1:165861635 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0192 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.100-28559_100-2854 others(19): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861635 | ||||||
| chr1:165861640 | AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0005g0305 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.100-28551_100-2854 others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861640 | ||||||
| chr1:165861641 | AAAAAAAA others(2): Show |
A | 27 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0002g0075 others(24): Show |
27 | HG00099.hp2 HG01192.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861641 | ||||||
| chr1:165861642 | AAAAAAAA others(1): Show |
A | 29 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0036 others(26): Show |
31 | HG01081.hp1 HG01081.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861642 | ||||||
| chr1:165861643 | AAAAAAAC | A | 37 | a0001c0001t0001g0299 a0001c0001t0002g0003 a0001c0001t0002g0017 others(34): Show |
37 | HG00323.hp2 HG00735.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(11): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861643 | ||||||
| chr1:165861644 | AAAAAAC | A | 17 | a0001c0001t0002g0095 a0001c0001t0002g0139 a0001c0001t0003g0044 others(14): Show |
17 | HG00673.hp1 HG00738.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861644 | ||||||
| chr1:165861645 | AAAAAC | A | 63 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0142 others(60): Show |
64 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.100-28554_100-2855 others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861645 | ||||||
| chr1:165861646 | AAAAC | A | 35 | a0001c0001t0001g0123 a0001c0001t0001g0236 a0001c0001t0001g0243 others(32): Show |
35 | HG00438.hp2 HG00735.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.100-28554_100-2855 others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861646 | ||||||
| chr1:165861649 | AC | A | 8 | a0001c0001t0002g0108 a0001c0001t0006g0104 a0001c0001t0006g0115 others(5): Show |
8 | HG01496.hp1 HG01891.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-28554delC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861649 | |||||||
| chr1:165861650 | C | A | 91 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.100-28554C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861650 | |||||||
| chr1:165861660 | C | A | 209 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(206): Show |
214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.100-28544C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861660 | |||||||
| chr1:165861737 | A | G | 56 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(53): Show |
59 | HG00099.hp2 HG00323.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.100-28467A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861737 | |||||||
| chr1:165861856 | C | T | 82 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0299 others(79): Show |
86 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.100-28348C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861856 | |||||||
| chr1:165861882 | G | C | 3 | a0001c0001t0009g0105 a0001c0001t0017g0004 a0002c0003t0009g0080 |
4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-28322G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861882 | |||||||
| chr1:165861891 | A | C | 97 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(94): Show |
98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.100-28313A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861891 | |||||||
| chr1:165862066 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.100-28138G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862066 | |||||||
| chr1:165862103 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.100-28101A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862103 | |||||||
| chr1:165862113 | C | T | 1 | a0001c0001t0006g0049 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-28091C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862113 | |||||||
| chr1:165862161 | T | C | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-28043T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862161 | |||||||
| chr1:165862163 | T | C | 1 | a0001c0002t0020g0198 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.100-28041T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862163 | |||||||
| chr1:165862168 | A | C | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-28036A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862168 | |||||||
| chr1:165862412 | A | G | 210 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(207): Show |
215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.100-27792A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862412 | |||||||
| chr1:165862585 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.100-27619G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862585 | |||||||
| chr1:165862681 | G | A | 1 | a0001c0001t0008g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.100-27523G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862681 | |||||||
| chr1:165862791 | C | A | 1 | a0001c0001t0012g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100-27413C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862791 | |||||||
| chr1:165862801 | G | A | 3 | a0001c0001t0009g0105 a0001c0001t0017g0004 a0002c0003t0009g0080 |
4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27403G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862801 | |||||||
| chr1:165862848 | G | T | 100 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0299 others(97): Show |
104 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.100-27356G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862848 | |||||||
| chr1:165862984 | C | G | 92 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0299 others(89): Show |
96 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-27220C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862984 | |||||||
| chr1:165863039 | C | G | 118 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(115): Show |
119 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.100-27165C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863039 | |||||||
| chr1:165863219 | C | G | 1 | a0001c0001t0009g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100-26985C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863219 | |||||||
| chr1:165863746 | G | T | 92 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0299 others(89): Show |
96 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-26458G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863746 | |||||||
| chr1:165863750 | T | G | 9 | a0001c0001t0002g0095 a0001c0001t0002g0139 a0001c0001t0002g0273 others(6): Show |
9 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-26454T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863750 | |||||||
| chr1:165863767 | A | G | 54 | a0001c0001t0001g0100 a0001c0001t0001g0181 a0001c0001t0001g0216 others(51): Show |
55 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.100-26437A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863767 | |||||||
| chr1:165863897 | A | G | 92 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0299 others(89): Show |
96 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-26307A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863897 | |||||||
| chr1:165863931 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0202 |
2 | HG02027.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.100-26273A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863931 | |||||||
| chr1:165863978 | CTTCTT | C | 3 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0294 |
3 | HG02717.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.100-26218_100-2621 others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165863978 | ||||||
| chr1:165863982 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-26222T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863982 | |||||||
| chr1:165863996 | G | A | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG00673.hp2 HG02523.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-26208G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863996 | |||||||
| chr1:165864011 | C | A | 210 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(207): Show |
215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.100-26193C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864011 | |||||||
| chr1:165864074 | AG | A | 98 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(95): Show |
99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-26129delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864074 | |||||||
| chr1:165864108 | T | C | 212 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(209): Show |
217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.100-26096T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864108 | |||||||
| chr1:165864133 | A | G | 4 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0004g0137 others(1): Show |
4 | HG02451.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-26071A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864133 | |||||||
| chr1:165864168 | G | A | 1 | a0001c0002t0005g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.100-26036G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864168 | |||||||
| chr1:165864195 | G | T | 1 | a0001c0001t0003g0034 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.100-26009G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864195 | |||||||
| chr1:165864239 | C | T | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-25965C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864239 | |||||||
| chr1:165864367 | G | T | 1 | a0001c0001t0006g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.100-25837G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864367 | |||||||
| chr1:165864625 | G | T | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-25579G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864625 | |||||||
| chr1:165864745 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0050 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100-25459T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864745 | |||||||
| chr1:165864821 | AG | A | 53 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(50): Show |
56 | HG00099.hp2 HG00323.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.100-25379delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165864821 | ||||||
| chr1:165864845 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-25359A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864845 | |||||||
| chr1:165864880 | T | G | 212 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(209): Show |
217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.100-25324T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864880 | |||||||
| chr1:165864886 | A | C | 211 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(208): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.100-25318A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864886 | |||||||
| chr1:165865015 | G | A | 211 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(208): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.100-25189G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865015 | |||||||
| chr1:165865150 | T | C | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-25054T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865150 | |||||||
| chr1:165865217 | G | A | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-24987G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865217 | |||||||
| chr1:165865252 | A | G | 24 | a0001c0001t0001g0299 a0001c0001t0002g0215 a0001c0001t0003g0208 others(21): Show |
24 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-24952A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865252 | |||||||
| chr1:165865368 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.100-24836G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865368 | |||||||
| chr1:165865573 | T | C | 13 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(10): Show |
13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-24631T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865573 | |||||||
| chr1:165865646 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0270 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.100-24558A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865646 | |||||||
| chr1:165865957 | A | G | 127 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(124): Show |
128 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.100-24247A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865957 | |||||||
| chr1:165865998 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.100-24206G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865998 | |||||||
| chr1:165866070 | G | A | 13 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(10): Show |
13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-24134G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866070 | |||||||
| chr1:165866127 | C | T | 215 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(212): Show |
220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.100-24077C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866127 | |||||||
| chr1:165866154 | A | G | 163 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(160): Show |
168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.100-24050A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866154 | |||||||
| chr1:165866218 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(62): Show |
68 | HG00323.hp2 HG00673.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.100-23986A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866218 | |||||||
| chr1:165866366 | C | T | 1 | a0001c0001t0030g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.100-23838C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866366 | |||||||
| chr1:165866489 | A | G | 24 | a0001c0001t0001g0299 a0001c0001t0002g0215 a0001c0001t0003g0208 others(21): Show |
24 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-23715A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866489 | |||||||
| chr1:165867118 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.100-23086T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867118 | |||||||
| chr1:165867155 | C | T | 10 | a0001c0001t0004g0011 a0001c0001t0004g0303 a0001c0001t0009g0062 others(7): Show |
10 | HG02145.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-23049C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867155 | |||||||
| chr1:165867199 | A | T | 2 | a0001c0001t0004g0015 a0001c0001t0004g0094 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.100-23005A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867199 | |||||||
| chr1:165867230 | T | C | 4 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0004g0137 others(1): Show |
4 | HG03098.hp1 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22974T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867230 | |||||||
| chr1:165867468 | T | A | 4 | a0001c0001t0006g0115 a0001c0001t0006g0116 a0001c0001t0006g0117 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22736T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867468 | |||||||
| chr1:165867512 | A | G | 13 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(10): Show |
13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-22692A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867512 | |||||||
| chr1:165867845 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100-22359A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867845 | |||||||
| chr1:165867957 | C | T | 4 | a0001c0001t0006g0107 a0001c0001t0006g0110 a0001c0001t0006g0295 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22247C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867957 | |||||||
| chr1:165868498 | G | A | 13 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(10): Show |
13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-21706G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868498 | |||||||
| chr1:165868578 | A | G | 1 | a0001c0001t0009g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100-21626A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868578 | |||||||
| chr1:165868625 | T | G | 6 | a0001c0001t0010g0093 a0001c0001t0010g0170 a0001c0001t0010g0247 others(3): Show |
6 | HG02132.hp2 HG02135.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-21579T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868625 | |||||||
| chr1:165868740 | T | A | 2 | a0001c0001t0024g0078 a0001c0001t0027g0084 |
2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.100-21464T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868740 | |||||||
| chr1:165868741 | C | T | 89 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(86): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.100-21463C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868741 | |||||||
| chr1:165868745 | G | A | 1 | a0001c0001t0009g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-21459G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868745 | |||||||
| chr1:165869033 | A | G | 1 | a0001c0001t0027g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-21171A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869033 | |||||||
| chr1:165869047 | C | A | 2 | a0001c0001t0004g0011 a0001c0001t0004g0303 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.100-21157C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869047 | |||||||
| chr1:165869091 | A | G | 1 | a0001c0001t0004g0311 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.100-21113A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869091 | |||||||
| chr1:165869138 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0124 |
2 | HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.100-21066C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869138 | |||||||
| chr1:165869151 | A | T | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-21053A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869151 | |||||||
| chr1:165869358 | AC | A | 10 | a0001c0001t0004g0011 a0001c0001t0004g0303 a0001c0001t0009g0062 others(7): Show |
10 | HG02145.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-20845delC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869358 | |||||||
| chr1:165869365 | A | G | 10 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(7): Show |
10 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-20839A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869365 | |||||||
| chr1:165869417 | T | G | 3 | a0001c0001t0006g0167 a0001c0001t0006g0168 a0001c0001t0006g0277 |
3 | HG02486.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.100-20787T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869417 | |||||||
| chr1:165869484 | T | G | 1 | a0001c0001t0007g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.100-20720T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869484 | |||||||
| chr1:165869622 | C | T | 1 | a0001c0002t0005g0235 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.100-20582C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869622 | |||||||
| chr1:165869644 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.100-20560A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869644 | |||||||
| chr1:165869659 | C | CT | 15 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0152 others(12): Show |
16 | HG01496.hp1 HG01515.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-20522dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | ||||||
| chr1:165869659 | C | CTT | 110 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.100-20523_100-2052 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | ||||||
| chr1:165869659 | C | CTTT | 17 | a0001c0001t0001g0098 a0001c0001t0001g0251 a0001c0001t0001g0289 others(14): Show |
17 | HG00673.hp2 HG01106.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-20524_100-2052 others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | ||||||
| chr1:165869659 | C | T | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-20545C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869659 | |||||||
| chr1:165869659 | CT | C | 133 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0142 others(130): Show |
137 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.100-20522delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | ||||||
| chr1:165869659 | CTT | C | 10 | a0001c0001t0001g0123 a0001c0001t0002g0017 a0001c0001t0002g0138 others(7): Show |
10 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-20523_100-2052 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | ||||||
| chr1:165869690 | TG | T | 256 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.100-20509delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869690 | ||||||
| chr1:165869713 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0270 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.100-20491C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869713 | |||||||
| chr1:165869784 | G | A | 1 | a0001c0002t0005g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-20420G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869784 | |||||||
| chr1:165869794 | T | C | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-20410T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869794 | |||||||
| chr1:165870196 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0149 a0001c0001t0001g0197 others(2): Show |
5 | NA18942.hp2 NA18964.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-20008A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870196 | |||||||
| chr1:165870201 | AT | A | 284 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(281): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.100-19984delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870201 | ||||||
| chr1:165870201 | ATT | A | 18 | a0001c0001t0003g0208 a0001c0001t0004g0059 a0001c0001t0004g0065 others(15): Show |
18 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-19985_100-1998 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870201 | ||||||
| chr1:165870260 | C | T | 6 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0004g0137 others(3): Show |
6 | HG03098.hp1 HG03453.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-19944C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870260 | |||||||
| chr1:165870263 | TAATTTTA others(108): Show |
T | 13 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(10): Show |
13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-19913_100-1979 others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870263 | ||||||
| chr1:165870291 | TTGCTCAC others(108): Show |
T | 1 | a0001c0001t0001g0033 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.100-19752_100-1963 others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870291 | ||||||
| chr1:165870313 | C | T | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-19891C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870313 | |||||||
| chr1:165870495 | A | G | 109 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(106): Show |
110 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.100-19709A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870495 | |||||||
| chr1:165870510 | T | C | 2 | a0001c0001t0019g0079 a0001c0001t0036g0136 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.100-19694T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870510 | |||||||
| chr1:165870777 | GT | G | 104 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(101): Show |
104 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.100-19426delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870777 | |||||||
| chr1:165870843 | A | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0009g0105 others(2): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-19361A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870843 | |||||||
| chr1:165870880 | C | T | 13 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(10): Show |
13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-19324C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870880 | |||||||
| chr1:165870903 | C | T | 5 | a0001c0001t0011g0040 a0001c0001t0011g0201 a0001c0001t0011g0220 others(2): Show |
5 | NA18944.hp2 NA18957.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-19301C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870903 | |||||||
| chr1:165870907 | G | A | 109 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(106): Show |
110 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.100-19297G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870907 | |||||||
| chr1:165871064 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.100-19140G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871064 | |||||||
| chr1:165871167 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0187 |
2 | HG02738.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.100-19037G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871167 | |||||||
| chr1:165871174 | C | T | 104 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(101): Show |
104 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.100-19030C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871174 | |||||||
| chr1:165871344 | A | G | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-18860A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871344 | |||||||
| chr1:165871387 | T | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0001t0001g0249 others(5): Show |
8 | HG01257.hp1 HG01258.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-18817T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871387 | |||||||
| chr1:165871591 | A | G | 1 | a0001c0001t0008g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.100-18613A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871591 | |||||||
| chr1:165871763 | C | T | 1 | a0001c0001t0037g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100-18441C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871763 | |||||||
| chr1:165872025 | C | CT | 124 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(122): Show |
intron_variant | MODIFIER | c.100-18167dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165872025 | ||||||
| chr1:165872036 | T | C | 1 | a0001c0001t0007g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.100-18168T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872036 | |||||||
| chr1:165872381 | T | G | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-17823T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872381 | |||||||
| chr1:165872517 | A | T | 3 | a0001c0001t0008g0030 a0001c0001t0008g0071 a0001c0001t0008g0072 |
3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100-17687A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872517 | |||||||
| chr1:165872531 | T | A | 4 | a0001c0001t0001g0131 a0001c0001t0001g0144 a0001c0001t0001g0233 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-17673T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872531 | |||||||
| chr1:165872531 | T | TA | 8 | a0001c0001t0002g0095 a0001c0001t0002g0139 a0001c0001t0002g0174 others(5): Show |
8 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-17667dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165872531 | ||||||
| chr1:165872776 | C | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0009g0105 others(2): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-17428C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872776 | |||||||
| chr1:165872777 | G | A | 12 | a0001c0001t0004g0011 a0001c0001t0004g0303 a0001c0001t0009g0062 others(9): Show |
12 | HG02145.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-17427G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872777 | |||||||
| chr1:165873042 | C | T | 1 | a0001c0001t0033g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-17162C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873042 | |||||||
| chr1:165873111 | C | T | 4 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0004g0137 others(1): Show |
4 | HG03098.hp1 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-17093C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873111 | |||||||
| chr1:165873158 | T | G | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-17046T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873158 | |||||||
| chr1:165873222 | C | T | 5 | a0001c0002t0005g0035 a0001c0002t0005g0077 a0001c0002t0005g0235 others(2): Show |
5 | HG02155.hp2 NA18747.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-16982C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873222 | |||||||
| chr1:165873488 | C | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.100-16716C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873488 | |||||||
| chr1:165873599 | C | T | 2 | a0001c0001t0019g0079 a0001c0001t0036g0136 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.100-16605C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873599 | |||||||
| chr1:165873759 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0009g0105 others(2): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-16445G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873759 | |||||||
| chr1:165873832 | C | T | 90 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(87): Show |
91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.100-16372C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873832 | |||||||
| chr1:165873838 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100-16366C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873838 | |||||||
| chr1:165874149 | CAG | C | 4 | a0001c0001t0009g0105 a0001c0001t0012g0012 a0001c0001t0017g0004 others(1): Show |
5 | HG02615.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-16054_100-1605 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874149 | |||||||
| chr1:165874209 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.100-15995C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874209 | |||||||
| chr1:165874438 | C | T | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-15766C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874438 | |||||||
| chr1:165874538 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0294 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.100-15666A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874538 | |||||||
| chr1:165874609 | A | G | 1 | a0001c0002t0005g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-15595A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874609 | |||||||
| chr1:165874786 | A | G | 3 | a0001c0001t0009g0105 a0001c0001t0017g0004 a0002c0003t0009g0080 |
4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-15418A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874786 | |||||||
| chr1:165874827 | T | A | 1 | a0001c0001t0033g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-15377T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874827 | |||||||
| chr1:165874859 | C | G | 9 | a0001c0001t0004g0137 a0001c0001t0009g0062 a0001c0001t0009g0063 others(6): Show |
9 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-15345C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874859 | |||||||
| chr1:165874895 | G | A | 1 | a0001c0001t0008g0016 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.100-15309G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874895 | |||||||
| chr1:165875038 | C | CAA | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-15150_100-1514 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165875038 | ||||||
| chr1:165875038 | CA | C | 117 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(114): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.100-15149delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165875038 | ||||||
| chr1:165875368 | T | A | 3 | a0001c0001t0008g0030 a0001c0001t0008g0071 a0001c0001t0008g0072 |
3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100-14836T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875368 | |||||||
| chr1:165875493 | G | C | 1 | a0001c0001t0003g0227 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100-14711G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875493 | |||||||
| chr1:165875695 | T | C | 9 | a0001c0001t0006g0067 a0001c0001t0006g0111 a0001c0001t0006g0119 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-14509T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875695 | |||||||
| chr1:165875748 | G | A | 1 | a0001c0001t0009g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-14456G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875748 | |||||||
| chr1:165875805 | C | T | 105 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-14399C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875805 | |||||||
| chr1:165875867 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-14337G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875867 | |||||||
| chr1:165876213 | C | A | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.100-13991C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876213 | |||||||
| chr1:165876237 | C | G | 2 | a0001c0001t0002g0043 a0001c0001t0002g0242 |
2 | HG03239.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.100-13967C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876237 | |||||||
| chr1:165876245 | G | A | 4 | a0001c0001t0002g0215 a0001c0001t0014g0018 a0001c0001t0014g0019 others(1): Show |
4 | NA19010.hp1 NA19062.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-13959G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876245 | |||||||
| chr1:165876317 | A | G | 1 | a0001c0001t0019g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-13887A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876317 | |||||||
| chr1:165876407 | T | C | 59 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(56): Show |
62 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.100-13797T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876407 | |||||||
| chr1:165876504 | A | G | 1 | a0001c0001t0002g0307 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-13700A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876504 | |||||||
| chr1:165876662 | A | G | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.100-13542A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876662 | |||||||
| chr1:165876781 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.100-13423A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876781 | |||||||
| chr1:165876890 | G | A | 3 | a0001c0001t0013g0083 a0001c0001t0013g0134 a0001c0001t0013g0315 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-13314G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876890 | |||||||
| chr1:165877189 | A | G | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-13015A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877189 | |||||||
| chr1:165877199 | G | T | 1 | a0001c0001t0009g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-13005G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877199 | |||||||
| chr1:165877278 | CATTTT | C | 105 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-12925_100-1292 others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877278 | |||||||
| chr1:165877432 | C | T | 1 | a0001c0001t0006g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100-12772C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877432 | |||||||
| chr1:165877441 | C | T | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-12763C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877441 | |||||||
| chr1:165877468 | C | T | 5 | a0001c0001t0011g0040 a0001c0001t0011g0201 a0001c0001t0011g0220 others(2): Show |
5 | NA18944.hp2 NA18957.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-12736C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877468 | |||||||
| chr1:165877470 | G | A | 7 | a0001c0001t0008g0016 a0001c0001t0008g0037 a0001c0001t0008g0046 others(4): Show |
7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-12734G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877470 | |||||||
| chr1:165877519 | G | T | 1 | a0001c0001t0019g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-12685G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877519 | |||||||
| chr1:165877575 | T | C | 1 | a0001c0001t0002g0001 | 3 | HG01081.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.100-12629T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877575 | |||||||
| chr1:165877616 | G | A | 1 | a0001c0001t0027g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-12588G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877616 | |||||||
| chr1:165877642 | G | A | 1 | a0001c0001t0009g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-12562G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877642 | |||||||
| chr1:165877643 | T | C | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-12561T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877643 | |||||||
| chr1:165878252 | T | C | 105 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-11952T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878252 | |||||||
| chr1:165878329 | T | C | 59 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(56): Show |
62 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.100-11875T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878329 | |||||||
| chr1:165878335 | CT | C | 105 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-11856delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165878335 | ||||||
| chr1:165878374 | G | A | 15 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(12): Show |
16 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-11830G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878374 | |||||||
| chr1:165878413 | C | T | 3 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0296 |
3 | HG02965.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-11791C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878413 | |||||||
| chr1:165878519 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-11685C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878519 | |||||||
| chr1:165878619 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.100-11585C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878619 | |||||||
| chr1:165878649 | C | T | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-11555C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878649 | |||||||
| chr1:165878712 | C | T | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-11492C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878712 | |||||||
| chr1:165879172 | G | A | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-11032G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879172 | |||||||
| chr1:165879447 | G | A | 2 | a0001c0001t0009g0062 a0001c0001t0009g0276 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.100-10757G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879447 | |||||||
| chr1:165879473 | A | G | 1 | a0001c0002t0005g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.100-10731A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879473 | |||||||
| chr1:165879545 | T | TTTA | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-10635_100-1063 others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTA | 8 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(5): Show |
8 | HG00673.hp1 HG02258.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-10638_100-1063 others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTAT others(2): Show |
9 | a0001c0001t0002g0070 a0001c0001t0002g0162 a0001c0001t0002g0270 others(6): Show |
9 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-10641_100-1063 others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTAT others(5): Show |
93 | a0001c0001t0001g0100 a0001c0001t0002g0001 a0001c0001t0002g0003 others(90): Show |
97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.100-10644_100-1063 others(16): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTAT others(8): Show |
23 | a0001c0001t0002g0043 a0001c0001t0002g0056 a0001c0001t0002g0096 others(20): Show |
23 | HG00639.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.100-10647_100-1063 others(19): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTAT others(11): Show |
32 | a0001c0001t0001g0052 a0001c0001t0001g0123 a0001c0001t0001g0142 others(29): Show |
33 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-10650_100-1063 others(22): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTAT others(14): Show |
11 | a0001c0001t0001g0172 a0001c0001t0003g0208 a0001c0001t0004g0175 others(8): Show |
11 | HG00140.hp2 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-10653_100-1063 others(25): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTAT others(17): Show |
1 | a0001c0001t0007g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-10656_100-1063 others(28): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879545 | T | TTTATTAT others(20): Show |
2 | a0001c0001t0004g0282 a0001c0001t0007g0053 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100-10633_100-1063 others(31): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | ||||||
| chr1:165879572 | T | A | 1 | a0001c0001t0004g0309 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.100-10632T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879572 | |||||||
| chr1:165879688 | T | G | 11 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(8): Show |
11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-10516T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879688 | |||||||
| chr1:165879819 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-10385A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879819 | |||||||
| chr1:165879976 | G | T | 200 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(197): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.100-10228G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879976 | |||||||
| chr1:165880062 | A | T | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-10142A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880062 | |||||||
| chr1:165880200 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.100-10004C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880200 | |||||||
| chr1:165880260 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.100-9944C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880260 | |||||||
| chr1:165880483 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-9721G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880483 | |||||||
| chr1:165880559 | TTTTGGGG others(3): Show |
T | 2 | a0001c0001t0008g0071 a0001c0001t0008g0072 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.100-9643_100-9634d others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880559 | ||||||
| chr1:165880560 | TTTGG | T | 4 | a0001c0001t0008g0016 a0001c0001t0008g0037 a0001c0001t0008g0046 others(1): Show |
4 | HG01192.hp2 HG02273.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-9643_100-9640d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880560 | |||||||
| chr1:165880562 | TGG | T | 37 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0048 others(34): Show |
37 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.100-9638_100-9637d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880562 | ||||||
| chr1:165880562 | TGGGGGTG others(6): Show |
T | 1 | a0001c0001t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.100-9641_100-9629d others(15): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | |||||||
| chr1:165880562 | TGGGGGTG others(10): Show |
T | 17 | a0001c0001t0001g0123 a0001c0001t0003g0209 a0001c0001t0003g0227 others(14): Show |
17 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-9641_100-9625d others(19): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | |||||||
| chr1:165880562 | TGGGGGTG others(12): Show |
T | 89 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0142 others(86): Show |
90 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.100-9641_100-9623d others(21): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | |||||||
| chr1:165880562 | TGGGGGTG others(14): Show |
T | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-9641_100-9621d others(23): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | |||||||
| chr1:165880563 | G | T | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-9641G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880563 | |||||||
| chr1:165880564 | GGGGT | G | 40 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0031 others(37): Show |
40 | HG00673.hp1 HG00733.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.100-9638_100-9635d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880564 | GGGGTGT | G | 16 | a0001c0001t0001g0055 a0001c0001t0001g0179 a0001c0001t0001g0187 others(13): Show |
16 | HG00099.hp1 HG01516.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-9638_100-9633d others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880564 | GGGGTGTG others(7): Show |
G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-9638_100-9625d others(16): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880564 | GGGGTGTG others(9): Show |
G | 1 | a0001c0001t0004g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-9638_100-9623d others(18): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880564 | GGGGTGTG others(11): Show |
G | 10 | a0001c0001t0001g0042 a0001c0001t0009g0014 a0001c0001t0009g0062 others(7): Show |
10 | HG02040.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-9638_100-9621d others(20): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880564 | GGGGTGTG others(15): Show |
G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0270 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.100-9638_100-9617d others(24): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880564 | GGGGTGTG others(19): Show |
G | 1 | a0001c0001t0002g0001 | 3 | HG01081.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.100-9638_100-9613d others(28): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880564 | GGGGTGTG others(21): Show |
G | 52 | a0001c0001t0002g0003 a0001c0001t0002g0017 a0001c0001t0002g0036 others(49): Show |
52 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.100-9638_100-9611d others(30): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | ||||||
| chr1:165880566 | G | T | 36 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0021 others(33): Show |
36 | HG00140.hp1 HG00738.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-9638G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880566 | |||||||
| chr1:165880566 | GGTGTGTG others(21): Show |
G | 1 | a0001c0001t0002g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.100-9616_100-9589d others(30): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880566 | ||||||
| chr1:165880567 | GTGTGTGT others(12): Show |
G | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-9636_100-9618d others(21): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880567 | |||||||
| chr1:165880578 | T | G | 1 | a0001c0001t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.100-9626T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880578 | |||||||
| chr1:165880582 | T | G | 17 | a0001c0001t0001g0123 a0001c0001t0003g0209 a0001c0001t0003g0227 others(14): Show |
17 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-9622T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880582 | |||||||
| chr1:165880584 | T | G | 89 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0142 others(86): Show |
90 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.100-9620T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880584 | |||||||
| chr1:165880586 | T | G | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-9618T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880586 | |||||||
| chr1:165880614 | T | A | 2 | a0001c0001t0019g0079 a0001c0001t0036g0136 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.100-9590T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880614 | |||||||
| chr1:165880719 | A | G | 1 | a0001c0001t0010g0261 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.100-9485A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880719 | |||||||
| chr1:165880872 | G | A | 1 | a0001c0001t0002g0307 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-9332G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880872 | |||||||
| chr1:165881083 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-9121G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881083 | |||||||
| chr1:165881133 | A | G | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-9071A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881133 | |||||||
| chr1:165881182 | T | TA | 119 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(116): Show |
119 | HG00099.hp1 HG00438.hp1 HG00733.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-8998dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165881182 | ||||||
| chr1:165881182 | T | TAA | 9 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0001t0001g0187 others(6): Show |
9 | HG02738.hp1 HG02738.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-8999_100-8998d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165881182 | ||||||
| chr1:165881182 | TA | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(62): Show |
68 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.100-8998delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165881182 | ||||||
| chr1:165881359 | T | G | 112 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(109): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.100-8845T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881359 | |||||||
| chr1:165881363 | G | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0187 |
2 | HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.100-8841G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881363 | |||||||
| chr1:165881461 | T | A | 3 | a0001c0001t0009g0105 a0001c0001t0017g0004 a0002c0003t0009g0080 |
4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-8743T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881461 | |||||||
| chr1:165881551 | G | T | 1 | a0001c0002t0005g0099 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-8653G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881551 | |||||||
| chr1:165881784 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100-8420G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881784 | |||||||
| chr1:165882447 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.100-7757T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882447 | |||||||
| chr1:165882559 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0219 a0001c0001t0003g0268 |
4 | HG00639.hp1 HG02300.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7645C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882559 | |||||||
| chr1:165882564 | A | G | 3 | a0001c0001t0009g0105 a0001c0001t0017g0004 a0002c0003t0009g0080 |
4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7640A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882564 | |||||||
| chr1:165882577 | G | T | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-7627G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882577 | |||||||
| chr1:165882588 | G | C | 11 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(8): Show |
11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-7616G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882588 | |||||||
| chr1:165882596 | C | A | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-7608C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882596 | |||||||
| chr1:165882807 | C | A | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-7397C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882807 | |||||||
| chr1:165882942 | G | A | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-7262G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882942 | |||||||
| chr1:165883038 | A | T | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-7166A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883038 | |||||||
| chr1:165883080 | T | C | 10 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0062 others(7): Show |
10 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-7124T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883080 | |||||||
| chr1:165883137 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.100-7067A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883137 | |||||||
| chr1:165883783 | C | T | 53 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(50): Show |
56 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.100-6421C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883783 | |||||||
| chr1:165883914 | C | T | 1 | a0001c0001t0017g0004 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-6290C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883914 | |||||||
| chr1:165883992 | T | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.100-6212T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883992 | |||||||
| chr1:165884065 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.100-6139G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884065 | |||||||
| chr1:165884116 | A | G | 10 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0062 others(7): Show |
10 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-6088A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884116 | |||||||
| chr1:165884246 | C | T | 10 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0062 others(7): Show |
10 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-5958C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884246 | |||||||
| chr1:165884330 | C | G | 15 | a0001c0001t0002g0017 a0001c0001t0002g0096 a0001c0001t0002g0138 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-5874C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884330 | |||||||
| chr1:165884368 | G | A | 1 | a0001c0001t0007g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.100-5836G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884368 | |||||||
| chr1:165884432 | C | G | 1 | a0001c0001t0010g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-5772C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884432 | |||||||
| chr1:165885040 | G | T | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-5164G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885040 | |||||||
| chr1:165885661 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100-4543G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885661 | |||||||
| chr1:165885705 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100-4499C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885705 | |||||||
| chr1:165885907 | A | G | 1 | a0001c0001t0017g0004 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-4297A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885907 | |||||||
| chr1:165886063 | G | A | 7 | a0001c0001t0008g0016 a0001c0001t0008g0037 a0001c0001t0008g0046 others(4): Show |
7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-4141G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886063 | |||||||
| chr1:165886085 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-4119G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886085 | |||||||
| chr1:165886161 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0089 a0001c0001t0001g0179 |
3 | HG00099.hp1 HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.100-4043T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886161 | |||||||
| chr1:165886270 | G | C | 1 | a0001c0001t0004g0282 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100-3934G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886270 | |||||||
| chr1:165886304 | AT | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-3893delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165886304 | ||||||
| chr1:165886352 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.100-3852T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886352 | |||||||
| chr1:165886522 | T | G | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-3682T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886522 | |||||||
| chr1:165886578 | C | T | 4 | a0001c0001t0009g0105 a0001c0001t0012g0012 a0001c0001t0017g0004 others(1): Show |
5 | HG02615.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-3626C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886578 | |||||||
| chr1:165886580 | C | T | 11 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(8): Show |
11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-3624C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886580 | |||||||
| chr1:165886883 | T | C | 67 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(64): Show |
70 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.100-3321T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886883 | |||||||
| chr1:165887078 | C | T | 57 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(54): Show |
60 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.100-3126C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887078 | |||||||
| chr1:165887138 | G | C | 1 | a0001c0001t0007g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.100-3066G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887138 | |||||||
| chr1:165887483 | G | A | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.100-2721G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887483 | |||||||
| chr1:165887543 | A | G | 3 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 |
3 | NA19062.hp1 NA19086.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.100-2661A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887543 | |||||||
| chr1:165887637 | G | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | NA18995.hp1 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.100-2567G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887637 | |||||||
| chr1:165887771 | T | TC | 109 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(106): Show |
110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.100-2425dupC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165887771 | ||||||
| chr1:165888135 | A | G | 3 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0296 |
3 | HG02965.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-2069A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888135 | |||||||
| chr1:165888247 | A | G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-1957A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888247 | |||||||
| chr1:165888432 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.100-1772C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888432 | |||||||
| chr1:165888434 | G | C | 11 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(8): Show |
11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-1770G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888434 | |||||||
| chr1:165888482 | G | A | 1 | a0001c0001t0007g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.100-1722G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888482 | |||||||
| chr1:165888642 | C | CT | 55 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(52): Show |
58 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.100-1538dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | ||||||
| chr1:165888642 | CT | C | 50 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0045 others(47): Show |
51 | HG00673.hp1 HG00733.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.100-1538delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | ||||||
| chr1:165888642 | CTT | C | 88 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0123 others(85): Show |
89 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.100-1539_100-1538d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | ||||||
| chr1:165888642 | CTTT | C | 8 | a0001c0001t0003g0032 a0001c0001t0003g0039 a0001c0001t0003g0087 others(5): Show |
8 | HG00323.hp1 HG02896.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-1540_100-1538d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | ||||||
| chr1:165888750 | T | C | 1 | a0001c0001t0008g0037 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.100-1454T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888750 | |||||||
| chr1:165888973 | G | C | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-1231G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888973 | |||||||
| chr1:165888999 | A | T | 2 | a0001c0001t0004g0015 a0001c0001t0004g0094 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.100-1205A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888999 | |||||||
| chr1:165889117 | C | T | 90 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.100-1087C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889117 | |||||||
| chr1:165889151 | G | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(52): Show |
58 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.100-1053G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889151 | |||||||
| chr1:165889216 | T | C | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-988T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889216 | |||||||
| chr1:165889232 | G | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(7): Show |
10 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-972G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889232 | |||||||
| chr1:165889504 | C | G | 1 | a0001c0001t0037g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100-700C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889504 | |||||||
| chr1:165889631 | T | C | 2 | a0001c0001t0004g0302 a0001c0001t0029g0132 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.100-573T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889631 | |||||||
| chr1:165889645 | C | T | 2 | a0001c0001t0016g0066 a0001c0001t0016g0286 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100-559C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889645 | |||||||
| chr1:165889669 | C | T | 2 | a0001c0001t0012g0012 a0001c0001t0012g0103 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-535C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889669 | |||||||
| chr1:165889688 | C | CT | 131 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.100-497dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165889688 | ||||||
| chr1:165889688 | CT | C | 18 | a0001c0001t0002g0178 a0001c0001t0003g0032 a0001c0001t0003g0041 others(15): Show |
18 | HG00323.hp1 HG01192.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-497delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165889688 | ||||||
| chr1:165889713 | A | T | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-491A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889713 | |||||||
| chr1:165889789 | C | T | 11 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0062 others(8): Show |
12 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-415C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889789 | |||||||
| chr1:165890146 | C | T | 1 | a0001c0001t0004g0303 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-58C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165890146 | |||||||
| chr1:165890381 | G | A | 1 | a0001c0001t0007g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259+18G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890381 | |||||||
| chr1:165890382 | G | T | 1 | a0001c0001t0007g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259+19G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890382 | |||||||
| chr1:165890403 | G | GTGT | 10 | a0001c0001t0002g0056 a0001c0001t0007g0023 a0001c0001t0007g0053 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+43_259+45dupTT others(1): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 165890403 | ||||||
| chr1:165890503 | G | A | 3 | a0001c0001t0003g0156 a0001c0001t0003g0158 a0001c0001t0003g0159 |
3 | HG01255.hp1 HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.259+140G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890503 | |||||||
| chr1:165890601 | G | A | 1 | a0001c0001t0007g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.259+238G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890601 | |||||||
| chr1:165890619 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.259+256G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890619 | |||||||
| chr1:165890717 | A | G | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259+354A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890717 | |||||||
| chr1:165890809 | A | C | 1 | a0001c0002t0015g0225 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.260-417A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890809 | |||||||
| chr1:165890863 | A | G | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260-363A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890863 | |||||||
| chr1:165890934 | A | C | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.260-292A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890934 | |||||||
| chr1:165891494 | G | A | 1 | a0001c0001t0009g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.356+172G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891494 | |||||||
| chr1:165891549 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.356+227C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891549 | |||||||
| chr1:165891569 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.356+247A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891569 | |||||||
| chr1:165891576 | A | C | 205 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(202): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.356+254A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891576 | |||||||
| chr1:165891623 | A | G | 1 | a0001c0002t0005g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.356+301A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891623 | |||||||
| chr1:165891630 | C | T | 204 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(201): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.356+308C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891630 | |||||||
| chr1:165891866 | T | G | 1 | a0001c0001t0010g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.356+544T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891866 | |||||||
| chr1:165891998 | C | T | 11 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0062 others(8): Show |
12 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.356+676C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891998 | |||||||
| chr1:165892002 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356+680T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892002 | |||||||
| chr1:165892146 | T | TCTGAAAC others(2353): Show |
2 | a0001c0001t0016g0066 a0001c0001t0016g0286 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.356+841_356+842ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2287): Show |
5 | a0001c0001t0006g0049 a0001c0001t0006g0107 a0001c0001t0006g0110 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2294): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2344): Show |
1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2351): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2349): Show |
1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2356): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2349): Show |
1 | a0001c0001t0001g0190 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2356): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0031 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0151 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0184 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0207 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2350): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0089 |
2 | HG01516.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2344): Show |
1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2351): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2350): Show |
14 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0045 others(11): Show |
14 | HG01257.hp1 HG01975.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0048 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0144 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0006g0283 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0086 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0130 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2300): Show |
1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2307): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0245 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2124): Show |
1 | a0001c0001t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2131): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2345): Show |
1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2352): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0019g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
6 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0100 others(3): Show |
6 | HG00099.hp1 HG00639.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0028 others(40): Show |
43 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
2 | a0001c0001t0001g0197 a0001c0001t0026g0240 |
2 | NA18964.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2311): Show |
3 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0243 |
3 | NA18951.hp2 NA19002.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2318): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0131 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
3 | a0001c0001t0001g0074 a0001c0001t0001g0189 a0001c0001t0001g0191 |
3 | NA18973.hp2 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0037g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0143 others(1): Show |
4 | HG00140.hp1 HG00741.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2353): Show |
1 | a0001c0001t0001g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0047 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0233 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2356): Show |
1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2363): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2355): Show |
1 | a0001c0001t0001g0192 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2362): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2313): Show |
1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2320): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2353): Show |
1 | a0001c0001t0001g0021 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0299 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2369): Show |
1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2376): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2126): Show |
1 | a0001c0001t0001g0239 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2133): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2352): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0194 |
2 | NA19064.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892146 | T | TCTGAAAC others(2353): Show |
1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | ||||||
| chr1:165892186 | G | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.356+864G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892186 | |||||||
| chr1:165892223 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.356+901C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892223 | |||||||
| chr1:165892224 | G | A | 1 | a0001c0002t0005g0235 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.356+902G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892224 | |||||||
| chr1:165892328 | G | A | 7 | a0001c0001t0008g0016 a0001c0001t0008g0037 a0001c0001t0008g0046 others(4): Show |
7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.356+1006G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892328 | |||||||
| chr1:165892356 | T | C | 204 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(201): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.356+1034T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892356 | |||||||
| chr1:165892408 | C | A | 6 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0294 others(3): Show |
6 | HG02280.hp2 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+1086C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892408 | |||||||
| chr1:165892552 | C | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.356+1230C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892552 | |||||||
| chr1:165892608 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.356+1286G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892608 | |||||||
| chr1:165892677 | C | G | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.356+1355C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892677 | |||||||
| chr1:165892849 | G | A | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.356+1527G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892849 | |||||||
| chr1:165893027 | C | T | 61 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(58): Show |
64 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.356+1705C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165893027 | |||||||
| chr1:165893034 | A | G | 2 | a0001c0001t0012g0012 a0001c0001t0012g0103 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.356+1712A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165893034 | |||||||
| chr1:165893086 | T | A | 131 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.356+1764T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165893086 | |||||||
| chr1:165894026 | T | A | 3 | a0001c0001t0004g0137 a0001c0001t0009g0014 a0001c0001t0009g0296 |
3 | HG02965.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.357-2164T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894026 | |||||||
| chr1:165894392 | T | G | 3 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0294 |
3 | HG02717.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.357-1798T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894392 | |||||||
| chr1:165894417 | A | G | 1 | a0001c0001t0006g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.357-1773A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894417 | |||||||
| chr1:165894449 | A | G | 3 | a0001c0001t0008g0030 a0001c0001t0008g0071 a0001c0001t0008g0072 |
3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.357-1741A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894449 | |||||||
| chr1:165894485 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0251 |
2 | NA19002.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.357-1705C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894485 | |||||||
| chr1:165894671 | T | C | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.357-1519T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894671 | |||||||
| chr1:165894676 | G | A | 2 | a0001c0001t0002g0174 a0001c0001t0003g0308 |
2 | HG04199.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.357-1514G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894676 | |||||||
| chr1:165894689 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.357-1501C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894689 | |||||||
| chr1:165894716 | C | A | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.357-1474C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894716 | |||||||
| chr1:165895071 | C | A | 198 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(195): Show |
202 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.357-1119C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895071 | |||||||
| chr1:165895137 | A | G | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.357-1053A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895137 | |||||||
| chr1:165895243 | G | A | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.357-947G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895243 | |||||||
| chr1:165895450 | T | A | 131 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.357-740T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895450 | |||||||
| chr1:165895607 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.357-583G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895607 | |||||||
| chr1:165895742 | G | A | 3 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0294 |
3 | HG02717.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.357-448G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895742 | |||||||
| chr1:165896023 | G | A | 1 | a0001c0002t0005g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.357-167G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165896023 | |||||||
| chr1:165896063 | G | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(53): Show |
59 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.357-127G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165896063 | |||||||
| chr1:165896457 | G | A | 120 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(117): Show |
120 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.499+125G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896457 | |||||||
| chr1:165896536 | G | C | 1 | a0001c0001t0010g0247 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.499+204G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896536 | |||||||
| chr1:165896864 | A | G | 1 | a0001c0001t0006g0283 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.499+532A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896864 | |||||||
| chr1:165896870 | T | C | 10 | a0001c0001t0009g0014 a0001c0001t0009g0062 a0001c0001t0009g0063 others(7): Show |
11 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.499+538T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896870 | |||||||
| chr1:165896976 | A | C | 3 | a0001c0001t0004g0118 a0001c0001t0004g0302 a0001c0001t0029g0132 |
3 | HG02280.hp2 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.499+644A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896976 | |||||||
| chr1:165896990 | C | T | 1 | a0001c0001t0033g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.499+658C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896990 | |||||||
| chr1:165897059 | C | T | 1 | a0001c0001t0008g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.499+727C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897059 | |||||||
| chr1:165897212 | G | T | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.499+880G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897212 | |||||||
| chr1:165897364 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.499+1032C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897364 | |||||||
| chr1:165897478 | G | A | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0096 |
3 | HG02735.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.499+1146G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897478 | |||||||
| chr1:165897652 | C | T | 57 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(54): Show |
60 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.499+1320C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897652 | |||||||
| chr1:165897711 | C | T | 2 | a0001c0001t0012g0012 a0001c0001t0012g0103 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.499+1379C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897711 | |||||||
| chr1:165897889 | A | C | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.499+1557A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897889 | |||||||
| chr1:165897931 | A | G | 38 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(35): Show |
39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1599A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897931 | |||||||
| chr1:165898205 | C | T | 216 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.499+1873C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898205 | |||||||
| chr1:165898248 | GGC | G | 38 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(35): Show |
39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1917_499+1918d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898248 | |||||||
| chr1:165898252 | A | C | 38 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(35): Show |
39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1920A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898252 | |||||||
| chr1:165898253 | A | C | 38 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(35): Show |
39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1921A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898253 | |||||||
| chr1:165898256 | GTGCAAAT others(1): Show |
G | 38 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(35): Show |
39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1925_499+1932d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898256 | |||||||
| chr1:165898263 | T | C | 1 | a0001c0001t0008g0232 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.499+1931T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898263 | |||||||
| chr1:165898266 | G | A | 58 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(55): Show |
61 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.499+1934G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898266 | |||||||
| chr1:165898375 | C | T | 2 | a0001c0001t0012g0012 a0001c0001t0012g0103 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.499+2043C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898375 | |||||||
| chr1:165898400 | T | C | 18 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0107 others(15): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.499+2068T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898400 | |||||||
| chr1:165898503 | C | T | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2171C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898503 | |||||||
| chr1:165898509 | T | C | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2177T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898509 | |||||||
| chr1:165898590 | C | T | 2 | a0001c0001t0012g0163 a0001c0001t0012g0280 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.499+2258C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898590 | |||||||
| chr1:165898618 | G | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2286G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898618 | |||||||
| chr1:165898746 | C | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2414C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898746 | |||||||
| chr1:165898780 | T | A | 38 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(35): Show |
39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+2448T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898780 | |||||||
| chr1:165898833 | C | T | 1 | a0001c0002t0015g0225 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.499+2501C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898833 | |||||||
| chr1:165898932 | T | C | 204 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(201): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.499+2600T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898932 | |||||||
| chr1:165898970 | T | C | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2638T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898970 | |||||||
| chr1:165899094 | T | G | 1 | a0001c0001t0012g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.499+2762T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899094 | |||||||
| chr1:165899259 | T | C | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2927T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899259 | |||||||
| chr1:165899308 | C | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2976C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899308 | |||||||
| chr1:165899309 | T | C | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2977T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899309 | |||||||
| chr1:165899332 | G | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+3000G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899332 | |||||||
| chr1:165899380 | A | G | 1 | a0001c0001t0023g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.499+3048A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899380 | |||||||
| chr1:165899468 | A | C | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+3136A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899468 | |||||||
| chr1:165899509 | T | C | 1 | a0001c0001t0002g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.499+3177T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899509 | |||||||
| chr1:165899529 | A | G | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+3197A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899529 | |||||||
| chr1:165899650 | T | C | 48 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(45): Show |
49 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.499+3318T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899650 | |||||||
| chr1:165899658 | C | T | 7 | a0001c0001t0008g0016 a0001c0001t0008g0037 a0001c0001t0008g0046 others(4): Show |
7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+3326C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899658 | |||||||
| chr1:165899733 | G | C | 5 | a0001c0001t0008g0037 a0001c0001t0008g0046 a0001c0001t0008g0153 others(2): Show |
5 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+3401G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899733 | |||||||
| chr1:165899801 | A | C | 48 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(45): Show |
49 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.500-3381A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899801 | |||||||
| chr1:165899850 | C | G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0144 others(2): Show |
5 | HG00733.hp2 HG01070.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-3332C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899850 | |||||||
| chr1:165899896 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.500-3286T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899896 | |||||||
| chr1:165899932 | A | G | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-3250A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899932 | |||||||
| chr1:165900013 | A | G | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-3169A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900013 | |||||||
| chr1:165900040 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.500-3142C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900040 | |||||||
| chr1:165900063 | G | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-3119G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900063 | |||||||
| chr1:165900081 | G | A | 3 | a0001c0001t0008g0030 a0001c0001t0008g0071 a0001c0001t0008g0072 |
3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.500-3101G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900081 | |||||||
| chr1:165900110 | G | A | 2 | a0001c0001t0002g0138 a0001c0001t0002g0160 |
2 | NA20129.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.500-3072G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900110 | |||||||
| chr1:165900130 | T | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-3052T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900130 | |||||||
| chr1:165900183 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.500-2999C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900183 | |||||||
| chr1:165900194 | T | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(70): Show |
76 | HG00673.hp1 HG01070.hp2 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.500-2988T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900194 | |||||||
| chr1:165900235 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.500-2947G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900235 | |||||||
| chr1:165900356 | G | T | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2826G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900356 | |||||||
| chr1:165900374 | T | C | 5 | a0001c0001t0006g0104 a0001c0001t0006g0115 a0001c0001t0006g0116 others(2): Show |
5 | HG01891.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-2808T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900374 | |||||||
| chr1:165900376 | T | C | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2806T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900376 | |||||||
| chr1:165900453 | T | A | 92 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-2729T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900453 | |||||||
| chr1:165900605 | A | G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.500-2577A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900605 | |||||||
| chr1:165900665 | GT | G | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2515delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165900665 | ||||||
| chr1:165900714 | G | A | 23 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(20): Show |
23 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.500-2468G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900714 | |||||||
| chr1:165900834 | A | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-2348A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900834 | |||||||
| chr1:165900854 | G | C | 1 | a0001c0001t0002g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.500-2328G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900854 | |||||||
| chr1:165901026 | T | C | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2156T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901026 | |||||||
| chr1:165901066 | G | A | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-2116G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901066 | |||||||
| chr1:165901070 | C | T | 36 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(33): Show |
37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-2112C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901070 | |||||||
| chr1:165901076 | C | T | 6 | a0001c0001t0001g0152 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
6 | HG01257.hp1 HG01258.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-2106C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901076 | |||||||
| chr1:165901152 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.500-2030G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901152 | |||||||
| chr1:165901257 | T | G | 2 | a0001c0001t0004g0015 a0001c0001t0004g0094 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.500-1925T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901257 | |||||||
| chr1:165901260 | C | T | 2 | a0001c0001t0016g0066 a0001c0001t0016g0286 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.500-1922C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901260 | |||||||
| chr1:165901286 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(73): Show |
79 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.500-1896G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901286 | |||||||
| chr1:165901292 | C | T | 3 | a0001c0001t0012g0163 a0001c0001t0012g0280 a0001c0001t0033g0010 |
3 | HG02559.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.500-1890C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901292 | |||||||
| chr1:165901325 | G | A | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.500-1857G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901325 | |||||||
| chr1:165901329 | A | G | 122 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(119): Show |
126 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.500-1853A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901329 | |||||||
| chr1:165901422 | C | T | 73 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(70): Show |
76 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.500-1760C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901422 | |||||||
| chr1:165901431 | G | T | 313 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.500-1751G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901431 | |||||||
| chr1:165901546 | C | A | 2 | a0001c0001t0003g0218 a0001c0001t0003g0308 |
2 | HG01433.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.500-1636C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901546 | |||||||
| chr1:165901563 | T | C | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-1619T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901563 | |||||||
| chr1:165901593 | A | G | 36 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(33): Show |
37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-1589A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901593 | |||||||
| chr1:165901611 | T | C | 5 | a0001c0001t0006g0049 a0001c0001t0006g0107 a0001c0001t0006g0110 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-1571T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901611 | |||||||
| chr1:165901636 | G | A | 3 | a0001c0001t0012g0163 a0001c0001t0012g0280 a0001c0001t0033g0010 |
3 | HG02559.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.500-1546G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901636 | |||||||
| chr1:165901693 | A | G | 2 | a0001c0001t0007g0090 a0001c0001t0007g0091 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.500-1489A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901693 | |||||||
| chr1:165901782 | T | C | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-1400T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901782 | |||||||
| chr1:165901818 | A | C | 3 | a0001c0001t0013g0083 a0001c0001t0013g0134 a0001c0001t0013g0315 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.500-1364A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901818 | |||||||
| chr1:165901852 | A | G | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.500-1330A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901852 | |||||||
| chr1:165901947 | C | CA | 156 | a0001c0001t0001g0031 a0001c0001t0002g0001 a0001c0001t0002g0003 others(153): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.500-1217dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165901947 | ||||||
| chr1:165901947 | C | CAA | 34 | a0001c0001t0002g0076 a0001c0001t0002g0096 a0001c0001t0002g0211 others(31): Show |
34 | HG00323.hp1 HG01433.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.500-1218_500-1217d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165901947 | ||||||
| chr1:165901947 | C | CAAA | 21 | a0001c0001t0006g0104 a0001c0001t0006g0115 a0001c0001t0006g0116 others(18): Show |
22 | HG01891.hp1 HG02451.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.500-1219_500-1217d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165901947 | ||||||
| chr1:165902031 | C | G | 168 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(165): Show |
172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.500-1151C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902031 | |||||||
| chr1:165902052 | G | A | 1 | a0001c0001t0002g0212 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.500-1130G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902052 | |||||||
| chr1:165902129 | G | A | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.500-1053G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902129 | |||||||
| chr1:165902148 | A | G | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.500-1034A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902148 | |||||||
| chr1:165902193 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0270 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.500-989G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902193 | |||||||
| chr1:165902371 | T | C | 36 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(33): Show |
37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-811T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902371 | |||||||
| chr1:165902428 | T | A | 2 | a0001c0001t0004g0011 a0001c0001t0004g0303 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.500-754T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902428 | |||||||
| chr1:165902437 | GA | G | 13 | a0001c0001t0004g0113 a0001c0001t0004g0302 a0001c0001t0009g0014 others(10): Show |
14 | HG02280.hp2 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.500-733delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902437 | ||||||
| chr1:165902442 | A | G | 1 | a0001c0001t0035g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.500-740A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902442 | |||||||
| chr1:165902468 | G | A | 74 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(71): Show |
77 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.500-714G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902468 | |||||||
| chr1:165902481 | G | A | 2 | a0001c0001t0012g0163 a0001c0001t0012g0280 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.500-701G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902481 | |||||||
| chr1:165902592 | A | AT | 53 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0041 others(50): Show |
54 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.500-563dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATT | 37 | a0001c0001t0003g0087 a0001c0001t0003g0122 a0001c0001t0003g0206 others(34): Show |
37 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-564_500-563dup others(2): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTT | 6 | a0001c0001t0007g0090 a0001c0001t0007g0157 a0001c0001t0019g0079 others(3): Show |
6 | HG01109.hp2 HG01515.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-565_500-563dup others(3): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(1): Show |
18 | a0001c0001t0002g0095 a0001c0001t0002g0109 a0001c0001t0002g0114 others(15): Show |
18 | HG00673.hp1 HG01070.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.500-570_500-563dup others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(2): Show |
15 | a0001c0001t0002g0174 a0001c0001t0002g0273 a0001c0001t0005g0005 others(12): Show |
15 | HG01071.hp1 HG01106.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.500-571_500-563dup others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(3): Show |
7 | a0001c0001t0002g0274 a0001c0001t0002g0294 a0001c0001t0025g0275 others(4): Show |
7 | HG01258.hp2 HG02080.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.500-572_500-563dup others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(4): Show |
26 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0033 others(23): Show |
26 | HG00099.hp1 HG00438.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.500-573_500-563dup others(11): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(5): Show |
24 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0027 others(21): Show |
24 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.500-574_500-563dup others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(6): Show |
15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0055 others(12): Show |
15 | HG00735.hp1 HG01496.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.500-575_500-563dup others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(7): Show |
8 | a0001c0001t0001g0073 a0001c0001t0001g0165 a0001c0001t0001g0185 others(5): Show |
8 | HG01515.hp2 HG01943.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-576_500-563dup others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0151 a0001c0001t0001g0184 |
3 | NA18954.hp1 NA18979.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.500-577_500-563dup others(15): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0180 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.500-578_500-563dup others(16): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0234 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.500-580_500-563dup others(18): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0047 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.500-582_500-563dup others(20): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0086 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500-583_500-563dup others(21): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | A | ATTTTTTT others(20): Show |
1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.500-589_500-563dup others(27): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | ATTTT | A | 30 | a0001c0001t0001g0050 a0001c0001t0001g0299 a0001c0001t0002g0001 others(27): Show |
33 | HG00323.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.500-566_500-563del others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | ATTTTTTT others(1): Show |
A | 8 | a0001c0001t0001g0098 a0001c0001t0001g0152 a0001c0001t0001g0249 others(5): Show |
8 | HG01257.hp1 HG01258.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-570_500-563del others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0004g0175 a0001c0001t0004g0214 a0001c0001t0004g0256 others(1): Show |
4 | NA18969.hp1 NA18992.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-574_500-563del others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902592 | ATTTTTTT others(6): Show |
A | 5 | a0001c0001t0003g0032 a0001c0001t0003g0034 a0001c0001t0003g0039 others(2): Show |
5 | NA18941.hp1 NA18945.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-575_500-563del others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | ||||||
| chr1:165902593 | T | A | 3 | a0001c0001t0006g0120 a0001c0001t0006g0121 a0001c0001t0006g0278 |
3 | HG01891.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.500-589T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902593 | |||||||
| chr1:165902634 | C | T | 1 | a0001c0001t0006g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-548C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902634 | |||||||
| chr1:165902744 | C | T | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.500-438C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902744 | |||||||
| chr1:165902768 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0192 |
2 | NA18985.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.500-414G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902768 | |||||||
| chr1:165902794 | C | T | 5 | a0001c0001t0006g0049 a0001c0001t0006g0107 a0001c0001t0006g0110 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-388C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902794 | |||||||
| chr1:165902830 | T | A | 1 | a0001c0001t0006g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.500-352T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902830 | |||||||
| chr1:165902880 | A | G | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.500-302A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902880 | |||||||
| chr1:165902900 | A | G | 4 | a0001c0001t0011g0040 a0001c0001t0011g0201 a0001c0001t0011g0220 others(1): Show |
4 | NA18944.hp2 NA18957.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-282A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902900 | |||||||
| chr1:165902922 | G | A | 5 | a0001c0001t0006g0049 a0001c0001t0006g0107 a0001c0001t0006g0110 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-260G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902922 | |||||||
| chr1:165902931 | C | T | 2 | a0001c0001t0016g0066 a0001c0001t0016g0286 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.500-251C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902931 | |||||||
| chr1:165903018 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.500-164C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165903018 | |||||||
| chr1:165903025 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.500-157G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165903025 | |||||||
| chr1:165903083 | T | C | 1 | a0001c0001t0004g0262 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.500-99T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165903083 | |||||||
| chr1:165903340 | C | T | 1 | a0001c0002t0005g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.597+61C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903340 | |||||||
| chr1:165903542 | A | G | 5 | a0001c0001t0001g0149 a0001c0001t0001g0197 a0001c0001t0001g0237 others(2): Show |
5 | NA18942.hp1 NA18964.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+263A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903542 | |||||||
| chr1:165903648 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | NA18973.hp2 NA18995.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+369A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903648 | |||||||
| chr1:165903668 | C | A | 31 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(28): Show |
34 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.597+389C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903668 | |||||||
| chr1:165903718 | C | T | 1 | a0001c0001t0009g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.597+439C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903718 | |||||||
| chr1:165904085 | G | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.597+806G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904085 | |||||||
| chr1:165904155 | T | C | 93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.597+876T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904155 | |||||||
| chr1:165904272 | C | G | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.597+993C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904272 | |||||||
| chr1:165904373 | A | G | 1 | a0001c0001t0012g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.597+1094A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904373 | |||||||
| chr1:165904382 | A | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(121): Show |
128 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.597+1103A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904382 | |||||||
| chr1:165904530 | T | G | 36 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(33): Show |
37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.597+1251T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904530 | |||||||
| chr1:165904537 | G | A | 26 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(23): Show |
26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.597+1258G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904537 | |||||||
| chr1:165904549 | C | T | 2 | a0001c0001t0012g0163 a0001c0001t0012g0280 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.597+1270C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904549 | |||||||
| chr1:165904703 | A | G | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.598-1218A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904703 | |||||||
| chr1:165904775 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.598-1146A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904775 | |||||||
| chr1:165904778 | T | C | 46 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(43): Show |
47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.598-1143T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904778 | |||||||
| chr1:165904791 | G | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.598-1130G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904791 | |||||||
| chr1:165905184 | G | A | 75 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(72): Show |
78 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.598-737G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165905184 | |||||||
| chr1:165905221 | G | A | 3 | a0001c0001t0002g0058 a0001c0001t0002g0092 a0001c0001t0002g0279 |
3 | HG02109.hp1 HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.598-700G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165905221 | |||||||
| chr1:165905675 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.598-246A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165905675 | |||||||
| chr1:165906057 | C | G | 4 | a0001c0001t0004g0175 a0001c0001t0004g0214 a0001c0001t0004g0256 others(1): Show |
4 | NA18969.hp1 NA18992.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+88C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906057 | |||||||
| chr1:165906272 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.646+303C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906272 | |||||||
| chr1:165906363 | A | G | 26 | a0001c0001t0006g0049 a0001c0001t0006g0067 a0001c0001t0006g0104 others(23): Show |
26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.646+394A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906363 | |||||||
| chr1:165906439 | C | T | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.646+470C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906439 | |||||||
| chr1:165906473 | A | G | 10 | a0001c0001t0008g0016 a0001c0001t0008g0030 a0001c0001t0008g0037 others(7): Show |
10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.646+504A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906473 | |||||||
| chr1:165906577 | T | A | 1 | a0001c0001t0006g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.646+608T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906577 | |||||||
| chr1:165906706 | A | G | 140 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0032 others(137): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.646+737A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906706 | |||||||
| chr1:165906726 | C | T | 2 | a0001c0001t0016g0066 a0001c0001t0016g0286 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.646+757C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906726 | |||||||
| chr1:165906735 | G | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.646+766G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906735 | |||||||
| chr1:165906890 | T | A | 1 | a0001c0001t0003g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.647-794T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906890 | |||||||
| chr1:165906940 | A | G | 2 | a0001c0001t0011g0145 a0001c0001t0011g0244 |
2 | NA19009.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.647-744A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906940 | |||||||
| chr1:165906947 | C | T | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.647-737C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906947 | |||||||
| chr1:165907033 | A | G | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647-651A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907033 | |||||||
| chr1:165907091 | G | A | 1 | a0001c0001t0032g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.647-593G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907091 | |||||||
| chr1:165907316 | G | A | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.647-368G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907316 | |||||||
| chr1:165907341 | C | T | 218 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(215): Show |
223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.647-343C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907341 | |||||||
| chr1:165907373 | CA | C | 3 | a0001c0001t0019g0079 a0001c0001t0024g0078 a0001c0001t0036g0136 |
3 | HG02451.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.647-310delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907373 | |||||||
| chr1:165907428 | G | T | 2 | a0001c0001t0016g0066 a0001c0001t0016g0286 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.647-256G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907428 | |||||||
| chr1:165907468 | A | G | 130 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0032 others(127): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.647-216A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907468 |