Item | Value |
---|---|
geneid | 256356 |
ensemblid | ENSG00000175066.16 |
hgncid | 28635 |
symbol | GK5 |
name | glycerol kinase 5 |
refseq_nuc | NM_001039547.3 |
refseq_prot | NP_001034636.1 |
ensembl_nuc | ENST00000392993.7 |
ensembl_prot | ENSP00000418001.1 |
mane_status | MANE Select |
chr | chr3 |
start | 142157527 |
end | 142225585 |
strand | - |
ver | v1.2 |
region | chr3:142157527-142225585 |
region5000 | chr3:142152527-142230585 |
regionname0 | GK5_chr3_142157527_142225585 |
regionname5000 | GK5_chr3_142152527_142230585 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 529 | 270 | 87 | 60 | 73 | 14 | 34 | 45 | GK5_chr3_142152527_142230585 | GK5 | MSGLL others(524): Show |
chr3 | 142152527 | 142230585 |
a0002 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | MSGLL others(524): Show |
chr3 | 142152527 | 142230585 |
a0003 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | MSGLL others(524): Show |
chr3 | 142152527 | 142230585 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1587 | 257 | 80 | 60 | 70 | 14 | 31 | GK5_chr3_142152527_142230585 | GK5 | ATGTC others(1582): Show |
chr3 | 142152527 | 142230585 | ||
a0001c0002 | 0/0 | 1587 | 12 | 6 | 0 | 3 | 0 | 3 | GK5_chr3_142152527_142230585 | GK5 | ATGTC others(1582): Show |
chr3 | 142152527 | 142230585 | ||
a0001c0003 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | ATGTC others(1582): Show |
chr3 | 142152527 | 142230585 | ||
a0002c0005 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | ATGTC others(1582): Show |
chr3 | 142152527 | 142230585 | ||
a0003c0004 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | ATGTC others(1582): Show |
chr3 | 142152527 | 142230585 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9815 | 106 | 16 | 29 | 42 | 2 | 16 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0002 | 0/0 | 9813 | 17 | 0 | 3 | 10 | 1 | 3 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0003 | 0/0 | 9816 | 15 | 9 | 5 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0004 | 0/0 | 9797 | 12 | 0 | 4 | 3 | 4 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9792): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0005 | 0/0 | 9833 | 6 | 6 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9828): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0006 | 0/0 | 9815 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0007 | 0/0 | 9811 | 6 | 5 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9806): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0008 | 0/0 | 9816 | 5 | 1 | 1 | 1 | 0 | 2 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0009 | 0/0 | 9815 | 4 | 0 | 4 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0010 | 0/0 | 9812 | 4 | 0 | 1 | 0 | 1 | 2 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9807): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0011 | 0/0 | 9808 | 4 | 4 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9803): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0012 | 0/0 | 9814 | 4 | 4 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9809): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0013 | 0/0 | 9813 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0014 | 0/0 | 9816 | 3 | 0 | 0 | 0 | 2 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0016 | 0/0 | 9812 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9807): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0017 | 0/0 | 9832 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9827): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0018 | 0/0 | 9838 | 2 | 1 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9833): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0019 | 0/0 | 9837 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9832): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0020 | 0/0 | 9837 | 2 | 1 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9832): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0021 | 0/0 | 9816 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0022 | 0/0 | 9814 | 2 | 1 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9809): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0023 | 0/0 | 9812 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9807): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0024 | 0/0 | 9815 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0025 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0026 | 0/0 | 9816 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0027 | 0/0 | 9814 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9809): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0028 | 0/0 | 9816 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0029 | 0/0 | 9812 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9807): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0030 | 0/0 | 9812 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9807): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0032 | 0/0 | 9816 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0033 | 0/0 | 9816 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0034 | 0/0 | 9827 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9822): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0035 | 0/0 | 9835 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9830): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0036 | 0/0 | 9834 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9829): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0037 | 0/0 | 9834 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9829): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0038 | 0/0 | 9831 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9826): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0039 | 0/0 | 9831 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9826): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0040 | 0/0 | 9833 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9828): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0041 | 0/0 | 9837 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9832): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0042 | 0/0 | 9836 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9831): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0043 | 0/0 | 9813 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0044 | 0/0 | 9815 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0045 | 0/0 | 9816 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0046 | 0/0 | 9816 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0047 | 0/0 | 9807 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9802): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0050 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0051 | 0/0 | 9816 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0052 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0053 | 0/0 | 9813 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0054 | 0/0 | 9814 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9809): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0055 | 0/1 | 9811 | 1 | 0 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9806): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0056 | 0/0 | 9815 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0057 | 0/0 | 9815 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0058 | 0/0 | 9816 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0059 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0060 | 0/0 | 9815 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0061 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0062 | 0/0 | 9815 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0063 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0064 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0065 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0066 | 0/0 | 9798 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9793): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0067 | 0/0 | 9815 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0068 | 0/0 | 9813 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0069 | 0/0 | 9815 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0070 | 0/0 | 9816 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0071 | 0/0 | 9834 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9829): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0072 | 0/0 | 9813 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0073 | 0/0 | 9813 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0074 | 0/0 | 9814 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9809): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0075 | 0/0 | 9811 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9806): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0076 | 0/0 | 9813 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0077 | 0/0 | 9815 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0001t0078 | 0/0 | 9812 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9807): Show |
chr3 | 142152527 | 142230585 |
a0001c0002t0003 | 0/0 | 9816 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0002t0006 | 0/0 | 9815 | 4 | 4 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0001c0002t0013 | 0/0 | 9813 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9808): Show |
chr3 | 142152527 | 142230585 |
a0001c0002t0015 | 0/0 | 9816 | 3 | 0 | 0 | 2 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0002t0031 | 0/0 | 9838 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9833): Show |
chr3 | 142152527 | 142230585 |
a0001c0002t0048 | 0/0 | 9816 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9811): Show |
chr3 | 142152527 | 142230585 |
a0001c0002t0049 | 0/0 | 9817 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9812): Show |
chr3 | 142152527 | 142230585 |
a0001c0003t0006 | 0/0 | 9815 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
a0002c0005t0017 | 0/0 | 9832 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9827): Show |
chr3 | 142152527 | 142230585 |
a0003c0004t0001 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | AGGCC others(9810): Show |
chr3 | 142152527 | 142230585 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0003 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0008g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0009g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0009g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0009g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0010g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0012g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0012g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0013g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0014g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0014g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0016g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0018g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0018g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0019g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0019g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0020g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0020g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0021g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0021g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0022g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0022g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0023g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0023g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0024g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0025g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0026g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0027g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0028g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0029g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0032g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0033g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0034g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0035g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0036g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0037g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0038g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0039g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0040g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0041g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0042g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0043g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0044g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0045g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0046g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0047g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0050g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0051g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0052g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0053g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0054g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0055g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0056g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0057g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0058g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0059g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0060g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0061g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0062g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0063g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0064g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0065g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0066g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0067g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0068g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0069g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0070g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0071g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0072g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0073g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0074g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0075g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0076g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0077g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0001t0078g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0015g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0015g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0015g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0031g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0048g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0002t0049g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0001c0003t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0002c0005t0017g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
a0003c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0010 | g0208 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00639 | hp1 | a0001 | c0001 | t0027 | g0107 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0207 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00738 | hp1 | a0001 | c0001 | t0045 | g0095 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG00741 | hp2 | a0001 | c0001 | t0078 | g0257 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01074 | hp2 | a0001 | c0001 | t0046 | g0155 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01109 | hp1 | a0001 | c0001 | t0077 | g0256 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01168 | hp2 | a0001 | c0001 | t0060 | g0083 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0175 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01243 | hp2 | a0001 | c0001 | t0018 | g0034 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01358 | hp2 | a0001 | c0001 | t0009 | g0033 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01361 | hp2 | a0001 | c0001 | t0044 | g0039 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0233 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01433 | hp2 | a0001 | c0001 | t0009 | g0171 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01496 | hp2 | a0001 | c0001 | t0020 | g0137 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01515 | hp1 | a0001 | c0001 | t0056 | g0243 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01516 | hp1 | a0001 | c0001 | t0024 | g0012 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01517 | hp2 | a0001 | c0001 | t0024 | g0012 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01891 | hp1 | a0001 | c0001 | t0012 | g0234 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01891 | hp2 | a0001 | c0001 | t0017 | g0149 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01934 | hp1 | a0001 | c0001 | t0028 | g0109 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01993 | hp1 | a0001 | c0001 | t0009 | g0110 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02004 | hp1 | a0001 | c0001 | t0009 | g0108 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02040 | hp1 | a0001 | c0001 | t0074 | g0222 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0163 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02056 | hp1 | a0001 | c0001 | t0008 | g0120 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02056 | hp2 | a0001 | c0001 | t0061 | g0182 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02083 | hp2 | a0001 | c0001 | t0072 | g0065 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02145 | hp1 | a0001 | c0001 | t0033 | g0154 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02145 | hp2 | a0001 | c0001 | t0070 | g0129 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0148 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02280 | hp1 | a0001 | c0001 | t0071 | g0141 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02300 | hp1 | a0001 | c0001 | t0069 | g0082 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02523 | hp1 | a0001 | c0001 | t0051 | g0081 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02523 | hp2 | a0001 | c0001 | t0052 | g0027 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02572 | hp2 | a0001 | c0001 | t0035 | g0115 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0242 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02615 | hp2 | a0001 | c0001 | t0026 | g0035 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02622 | hp1 | a0001 | c0001 | t0036 | g0037 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0117 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0145 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02630 | hp2 | a0001 | c0001 | t0076 | g0160 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02647 | hp2 | a0001 | c0001 | t0013 | g0238 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0231 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02723 | hp2 | a0001 | c0001 | t0016 | g0224 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02738 | hp1 | a0001 | c0001 | t0008 | g0250 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0177 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02809 | hp2 | a0001 | c0002 | t0031 | g0044 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02886 | hp1 | a0001 | c0001 | t0016 | g0151 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02895 | hp1 | a0001 | c0001 | t0019 | g0158 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0235 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02896 | hp1 | a0001 | c0002 | t0006 | g0219 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02896 | hp2 | a0001 | c0001 | t0021 | g0049 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0237 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02897 | hp2 | a0001 | c0001 | t0021 | g0050 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02965 | hp1 | a0001 | c0001 | t0042 | g0139 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02965 | hp2 | a0001 | c0001 | t0034 | g0147 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02970 | hp2 | a0002 | c0005 | t0017 | g0203 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0094 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02976 | hp2 | a0001 | c0003 | t0006 | g0161 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03017 | hp1 | a0001 | c0001 | t0022 | g0052 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03041 | hp1 | a0001 | c0001 | t0039 | g0150 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03098 | hp1 | a0001 | c0001 | t0023 | g0116 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03225 | hp1 | a0001 | c0001 | t0019 | g0114 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03225 | hp2 | a0001 | c0001 | t0053 | g0157 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03453 | hp1 | a0001 | c0001 | t0068 | g0159 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03486 | hp2 | a0001 | c0002 | t0006 | g0218 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03490 | hp1 | a0001 | c0001 | t0062 | g0112 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0097 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03540 | hp1 | a0001 | c0002 | t0013 | g0252 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0236 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03579 | hp2 | a0001 | c0001 | t0022 | g0214 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03704 | hp2 | a0001 | c0002 | t0049 | g0176 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03710 | hp2 | a0001 | c0001 | t0014 | g0133 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03831 | hp2 | a0001 | c0001 | t0010 | g0041 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03834 | hp1 | a0001 | c0001 | t0067 | g0190 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03927 | hp2 | a0001 | c0001 | t0058 | g0032 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03942 | hp1 | a0001 | c0001 | t0010 | g0125 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG04228 | hp1 | a0001 | c0002 | t0015 | g0216 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | CHB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18906 | hp1 | a0001 | c0001 | t0041 | g0140 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18906 | hp2 | a0001 | c0001 | t0040 | g0144 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18947 | hp2 | a0001 | c0002 | t0015 | g0187 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18948 | hp2 | a0001 | c0002 | t0048 | g0188 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18956 | hp1 | a0001 | c0001 | t0064 | g0087 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18982 | hp2 | a0001 | c0001 | t0025 | g0013 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18986 | hp1 | a0001 | c0001 | t0065 | g0017 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA18992 | hp2 | a0001 | c0001 | t0066 | g0026 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19009 | hp2 | a0001 | c0001 | t0073 | g0221 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19010 | hp1 | a0001 | c0001 | t0054 | g0103 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19030 | hp1 | a0001 | c0001 | t0030 | g0153 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19043 | hp1 | a0001 | c0001 | t0032 | g0232 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19064 | hp2 | a0001 | c0002 | t0015 | g0189 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19079 | hp2 | a0001 | c0001 | t0063 | g0196 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19083 | hp1 | a0001 | c0001 | t0059 | g0078 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19086 | hp1 | a0001 | c0001 | t0050 | g0227 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19091 | hp1 | a0003 | c0004 | t0001 | g0217 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20129 | hp1 | a0001 | c0001 | t0013 | g0255 | AFR | ASW | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20752 | hp2 | a0001 | c0001 | t0014 | g0131 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0185 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20805 | hp2 | a0001 | c0001 | t0014 | g0132 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20905 | hp1 | a0001 | c0001 | t0057 | g0186 | SAS | GIH | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20905 | hp2 | a0001 | c0001 | t0029 | g0042 | SAS | GIH | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01123 | hp1 | a0001 | c0001 | t0047 | g0096 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02109 | hp1 | a0001 | c0001 | t0020 | g0138 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0092 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02486 | hp1 | a0001 | c0001 | t0037 | g0038 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02559 | hp1 | a0001 | c0002 | t0006 | g0251 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03471 | hp1 | a0001 | c0001 | t0043 | g0239 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG03471 | hp2 | a0001 | c0002 | t0006 | g0220 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG06807 | hp1 | a0001 | c0001 | t0075 | g0093 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA21309 | hp1 | a0001 | c0001 | t0038 | g0143 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
homoSapiens | chm13v2 | a0001 | c0001 | t0055 | g0184 | REF | REF | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142172440 | G | A | 1 | a0003 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.1160C>T | p.Pro387Leu | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/16 | 1290/9815 | 1160/1590 | 387/529 | chr3 | 142172440 | |||
chr3:142182959 | T | C | 1 | a0002 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.907A>G | p.Ile303Val | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/16 | 1037/9815 | 907/1590 | 303/529 | chr3 | 142182959 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142181525 | G | A | 1 | a0001c0002 | 12 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(9): Show |
synonymous_variant | LOW | c.984C>T | p.Val328Val | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/16 | 1114/9815 | 984/1590 | 328/529 | chr3 | 142181525 | |||
chr3:142186503 | A | G | 1 | a0001c0003 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.630T>C | p.Tyr210Tyr | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/16 | 760/9815 | 630/1590 | 210/529 | chr3 | 142186503 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142157957 | G | GT | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(26): Show |
58 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*7664dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7664 | chr3 | 142157957 | ||||||
chr3:142158086 | G | A | 2 | a0001c0001t0030 a0001c0001t0033 |
2 | HG02145.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7536C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7536 | chr3 | 142158086 | ||||||
chr3:142158145 | G | A | 4 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0029 others(1): Show |
8 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7477C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7477 | chr3 | 142158145 | ||||||
chr3:142158242 | T | C | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*7380A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7380 | chr3 | 142158242 | ||||||
chr3:142158315 | T | G | 1 | a0001c0001t0059 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7307A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7307 | chr3 | 142158315 | ||||||
chr3:142158419 | T | C | 1 | a0001c0001t0075 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7203A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7203 | chr3 | 142158419 | ||||||
chr3:142158565 | T | G | 36 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(33): Show |
71 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*7057A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7057 | chr3 | 142158565 | ||||||
chr3:142158710 | G | C | 1 | a0001c0001t0039 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6912C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6912 | chr3 | 142158710 | ||||||
chr3:142158740 | A | G | 1 | a0001c0001t0063 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6882T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6882 | chr3 | 142158740 | ||||||
chr3:142158755 | C | T | 1 | a0001c0001t0057 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6867G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6867 | chr3 | 142158755 | ||||||
chr3:142158768 | G | A | 10 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(7): Show |
30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6854C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6854 | chr3 | 142158768 | ||||||
chr3:142158865 | C | A | 18 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(15): Show |
27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6757G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6757 | chr3 | 142158865 | ||||||
chr3:142158984 | A | T | 1 | a0001c0001t0056 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6638T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6638 | chr3 | 142158984 | ||||||
chr3:142159179 | G | T | 1 | a0001c0001t0054 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6443C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6443 | chr3 | 142159179 | ||||||
chr3:142159254 | C | CA | 5 | a0001c0001t0002 a0001c0001t0072 a0001c0001t0073 others(2): Show |
21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6367dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6367 | chr3 | 142159254 | ||||||
chr3:142159311 | G | A | 1 | a0001c0001t0060 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6311C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6311 | chr3 | 142159311 | ||||||
chr3:142159351 | A | G | 3 | a0001c0001t0010 a0001c0001t0029 a0001c0001t0078 |
6 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6271T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6271 | chr3 | 142159351 | ||||||
chr3:142159377 | G | A | 10 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(7): Show |
30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6245C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6245 | chr3 | 142159377 | ||||||
chr3:142159619 | G | C | 1 | a0001c0001t0029 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6003C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6003 | chr3 | 142159619 | ||||||
chr3:142159630 | TA | T | 36 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(33): Show |
67 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5991delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5991 | chr3 | 142159630 | ||||||
chr3:142159694 | G | A | 2 | a0001c0001t0041 a0001c0001t0042 |
2 | HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5928C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5928 | chr3 | 142159694 | ||||||
chr3:142159780 | C | T | 1 | a0001c0001t0046 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5842G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5842 | chr3 | 142159780 | ||||||
chr3:142159789 | G | A | 1 | a0001c0001t0023 | 2 | HG03098.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5833C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5833 | chr3 | 142159789 | ||||||
chr3:142159795 | G | A | 1 | a0001c0001t0072 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5827C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5827 | chr3 | 142159795 | ||||||
chr3:142159826 | G | A | 27 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0013 others(24): Show |
40 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*5796C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5796 | chr3 | 142159826 | ||||||
chr3:142159826 | GCTTTCTC others(1): Show |
G | 2 | a0001c0001t0011 a0001c0001t0047 |
5 | HG01123.hp1 HG02109.hp2 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5788_*5795delAGAG others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5788 | chr3 | 142159826 | ||||||
chr3:142159829 | T | C | 7 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0021 others(4): Show |
24 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5793A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5793 | chr3 | 142159829 | ||||||
chr3:142159829 | T | TTC | 2 | a0001c0001t0012 a0001c0002t0006 |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5791_*5792dupGA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5792 | chr3 | 142159829 | ||||||
chr3:142159829 | TTC | T | 3 | a0001c0001t0001 a0001c0001t0013 a0001c0002t0013 |
4 | HG02647.hp2 HG03540.hp1 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5791_*5792delGA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5791 | chr3 | 142159829 | ||||||
chr3:142159829 | TTCTC | T | 13 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(10): Show |
35 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*5789_*5792delGAGA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5789 | chr3 | 142159829 | ||||||
chr3:142159831 | C | T | 5 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0029 others(2): Show |
9 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5791G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5791 | chr3 | 142159831 | ||||||
chr3:142159841 | C | T | 7 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0021 others(4): Show |
24 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5781G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5781 | chr3 | 142159841 | ||||||
chr3:142159847 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG03041.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | ||||||
chr3:142159847 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0017 a0001c0001t0042 a0002c0005t0017 |
3 | HG01891.hp2 HG02965.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | ||||||
chr3:142159847 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0020 others(1): Show |
11 | HG01496.hp2 HG02109.hp1 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | ||||||
chr3:142159847 | C | CTTTTTTT others(14): Show |
3 | a0001c0001t0018 a0001c0001t0036 a0001c0001t0071 |
4 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | ||||||
chr3:142159847 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0035 a0001c0002t0031 |
2 | HG02572.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | ||||||
chr3:142159849 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0034 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5772_*5773insAAAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5772 | chr3 | 142159849 | ||||||
chr3:142159849 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0040 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5772_*5773insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5772 | chr3 | 142159849 | ||||||
chr3:142159849 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0037 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5772_*5773insAAAA others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5772 | chr3 | 142159849 | ||||||
chr3:142159849 | C | T | 16 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0017 others(13): Show |
27 | HG01123.hp1 HG01243.hp2 HG01496.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5773G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5773 | chr3 | 142159849 | ||||||
chr3:142159851 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0032 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5770_*5771insAAAA others(22): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5770 | chr3 | 142159851 | ||||||
chr3:142159851 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5770_*5771insAAAA others(24): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5770 | chr3 | 142159851 | ||||||
chr3:142159851 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0033 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5770_*5771insAAAA others(28): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5770 | chr3 | 142159851 | ||||||
chr3:142159851 | C | T | 19 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(16): Show |
28 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5771G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5771 | chr3 | 142159851 | ||||||
chr3:142159853 | C | CT | 4 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0054 others(1): Show |
9 | HG01099.hp1 HG01106.hp2 HG01256.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5768dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTCTCT others(7): Show |
1 | a0001c0001t0068 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTCTCT others(9): Show |
3 | a0001c0001t0010 a0001c0001t0029 a0001c0001t0078 |
5 | HG00099.hp1 HG00741.hp2 HG03831.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(12): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTCTCT others(10): Show |
1 | a0001c0001t0010 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTCTTT others(7): Show |
1 | a0001c0001t0016 | 2 | HG02723.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTTTTT others(6): Show |
1 | a0001c0001t0043 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(9): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTTTTT others(12): Show |
1 | a0001c0001t0007 | 6 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTTTTT others(13): Show |
1 | a0001c0001t0074 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTCTTTTT others(15): Show |
2 | a0001c0001t0072 a0001c0001t0075 |
2 | HG02083.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTT | 2 | a0001c0001t0004 a0001c0001t0066 |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5764_*5768dupAAAA others(1): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0023 | 2 | HG03098.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(9): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0076 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0073 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002 | 12 | HG00140.hp1 HG00408.hp2 HG01256.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0002 | 3 | HG01069.hp2 HG02071.hp2 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(19): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | ||||||
chr3:142159853 | C | T | 22 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(19): Show |
31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5769G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5769 | chr3 | 142159853 | ||||||
chr3:142159855 | T | C | 1 | a0001c0001t0061 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5767A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5767 | chr3 | 142159855 | ||||||
chr3:142159871 | A | G | 5 | a0001c0001t0002 a0001c0001t0072 a0001c0001t0073 others(2): Show |
21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5751T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5751 | chr3 | 142159871 | ||||||
chr3:142159908 | C | A | 10 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(7): Show |
30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5714G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5714 | chr3 | 142159908 | ||||||
chr3:142159932 | C | T | 1 | a0001c0001t0076 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5690G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5690 | chr3 | 142159932 | ||||||
chr3:142159936 | G | A | 1 | a0001c0001t0062 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5686C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5686 | chr3 | 142159936 | ||||||
chr3:142159983 | G | A | 1 | a0001c0001t0020 | 2 | HG01496.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5639C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5639 | chr3 | 142159983 | ||||||
chr3:142160128 | G | A | 24 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0013 others(21): Show |
44 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5494C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5494 | chr3 | 142160128 | ||||||
chr3:142160132 | G | A | 1 | a0001c0001t0043 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5490C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5490 | chr3 | 142160132 | ||||||
chr3:142160393 | C | G | 1 | a0001c0001t0043 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5229G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5229 | chr3 | 142160393 | ||||||
chr3:142160398 | A | G | 1 | a0001c0001t0075 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5224T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5224 | chr3 | 142160398 | ||||||
chr3:142160536 | T | C | 1 | a0001c0001t0023 | 2 | HG03098.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5086A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5086 | chr3 | 142160536 | ||||||
chr3:142160618 | G | C | 22 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(19): Show |
31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5004C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5004 | chr3 | 142160618 | ||||||
chr3:142160809 | C | A | 26 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0013 others(23): Show |
39 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4813G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4813 | chr3 | 142160809 | ||||||
chr3:142160896 | A | T | 1 | a0001c0001t0076 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4726T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4726 | chr3 | 142160896 | ||||||
chr3:142160915 | G | T | 1 | a0001c0001t0007 | 6 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4707C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4707 | chr3 | 142160915 | ||||||
chr3:142161078 | CTTTTGTT others(7): Show |
C | 2 | a0001c0001t0004 a0001c0001t0066 |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4530_*4543delACAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4530 | chr3 | 142161078 | ||||||
chr3:142161079 | T | G | 3 | a0001c0001t0030 a0001c0001t0032 a0001c0001t0033 |
3 | HG02145.hp1 NA19030.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4543A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4543 | chr3 | 142161079 | ||||||
chr3:142161084 | TTTTTTTG | T | 5 | a0001c0001t0002 a0001c0001t0072 a0001c0001t0073 others(2): Show |
21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4531_*4537delCAAA others(3): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4531 | chr3 | 142161084 | ||||||
chr3:142161090 | TG | T | 28 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0010 others(25): Show |
47 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4531delC | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4531 | chr3 | 142161090 | ||||||
chr3:142161091 | G | T | 13 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(10): Show |
36 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4531C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4531 | chr3 | 142161091 | ||||||
chr3:142161097 | G | T | 1 | a0001c0001t0021 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4525C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4525 | chr3 | 142161097 | ||||||
chr3:142161163 | G | A | 5 | a0001c0001t0002 a0001c0001t0072 a0001c0001t0073 others(2): Show |
21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4459C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4459 | chr3 | 142161163 | ||||||
chr3:142161479 | C | T | 1 | a0001c0001t0034 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4143G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4143 | chr3 | 142161479 | ||||||
chr3:142161491 | A | G | 2 | a0001c0001t0004 a0001c0001t0066 |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4131T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4131 | chr3 | 142161491 | ||||||
chr3:142161582 | G | C | 2 | a0001c0001t0014 a0001c0001t0046 |
4 | HG01074.hp2 HG03710.hp2 NA20752.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4040C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4040 | chr3 | 142161582 | ||||||
chr3:142161617 | T | G | 1 | a0001c0001t0073 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4005A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4005 | chr3 | 142161617 | ||||||
chr3:142161624 | C | T | 1 | a0001c0001t0075 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3998G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3998 | chr3 | 142161624 | ||||||
chr3:142161789 | T | TATTG | 8 | a0001c0001t0018 a0001c0001t0019 a0001c0001t0020 others(5): Show |
11 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3829_*3832dupCAAT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3832 | chr3 | 142161789 | ||||||
chr3:142161811 | T | C | 1 | a0001c0001t0047 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3811A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3811 | chr3 | 142161811 | ||||||
chr3:142161997 | G | A | 7 | a0001c0001t0006 a0001c0001t0077 a0001c0002t0006 others(4): Show |
12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3625C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3625 | chr3 | 142161997 | ||||||
chr3:142162366 | G | C | 18 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(15): Show |
27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3256C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3256 | chr3 | 142162366 | ||||||
chr3:142162509 | T | C | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*3113A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3113 | chr3 | 142162509 | ||||||
chr3:142162517 | G | A | 1 | a0001c0001t0063 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3105C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3105 | chr3 | 142162517 | ||||||
chr3:142162749 | G | A | 3 | a0001c0002t0015 a0001c0002t0048 a0001c0002t0049 |
5 | HG03704.hp2 HG04228.hp1 NA18947.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2873C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2873 | chr3 | 142162749 | ||||||
chr3:142162763 | C | T | 1 | a0001c0002t0048 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2859G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2859 | chr3 | 142162763 | ||||||
chr3:142162926 | A | G | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2696T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2696 | chr3 | 142162926 | ||||||
chr3:142162945 | G | A | 1 | a0001c0001t0073 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2677C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2677 | chr3 | 142162945 | ||||||
chr3:142162995 | C | CA | 13 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 others(10): Show |
37 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2626dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2626 | chr3 | 142162995 | ||||||
chr3:142162995 | CA | C | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(33): Show |
81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2626delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2626 | chr3 | 142162995 | ||||||
chr3:142163032 | C | T | 1 | a0001c0001t0052 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2590G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2590 | chr3 | 142163032 | ||||||
chr3:142163037 | T | C | 1 | a0001c0001t0064 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2585A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2585 | chr3 | 142163037 | ||||||
chr3:142163085 | T | C | 1 | a0001c0001t0065 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2537A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2537 | chr3 | 142163085 | ||||||
chr3:142163114 | T | C | 2 | a0001c0001t0004 a0001c0001t0066 |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2508A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2508 | chr3 | 142163114 | ||||||
chr3:142163265 | A | G | 5 | a0001c0001t0002 a0001c0001t0072 a0001c0001t0073 others(2): Show |
21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2357T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2357 | chr3 | 142163265 | ||||||
chr3:142163277 | C | CT | 4 | a0001c0001t0051 a0001c0002t0015 a0001c0002t0048 others(1): Show |
6 | HG02523.hp1 HG03704.hp2 HG04228.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2344dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2344 | chr3 | 142163277 | ||||||
chr3:142163277 | CT | C | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2344delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2344 | chr3 | 142163277 | ||||||
chr3:142163297 | C | T | 8 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0023 others(5): Show |
30 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2325G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2325 | chr3 | 142163297 | ||||||
chr3:142163303 | G | A | 2 | a0001c0001t0007 a0001c0001t0075 |
7 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2319C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2319 | chr3 | 142163303 | ||||||
chr3:142163305 | C | T | 1 | a0001c0001t0050 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2317G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2317 | chr3 | 142163305 | ||||||
chr3:142163403 | TA | T | 2 | a0001c0001t0004 a0001c0001t0066 |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2218delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2218 | chr3 | 142163403 | ||||||
chr3:142163617 | C | T | 35 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(32): Show |
70 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2005G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2005 | chr3 | 142163617 | ||||||
chr3:142163801 | C | T | 7 | a0001c0001t0006 a0001c0001t0077 a0001c0002t0006 others(4): Show |
12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1821G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1821 | chr3 | 142163801 | ||||||
chr3:142163813 | C | T | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1809G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1809 | chr3 | 142163813 | ||||||
chr3:142164189 | T | C | 2 | a0001c0001t0004 a0001c0001t0066 |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1433A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1433 | chr3 | 142164189 | ||||||
chr3:142164213 | A | C | 3 | a0001c0001t0009 a0001c0001t0027 a0001c0001t0028 |
6 | HG00639.hp1 HG01358.hp2 HG01433.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1409T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1409 | chr3 | 142164213 | ||||||
chr3:142164496 | G | A | 1 | a0001c0001t0067 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1126C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1126 | chr3 | 142164496 | ||||||
chr3:142164570 | T | C | 1 | a0001c0001t0068 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1052 | chr3 | 142164570 | ||||||
chr3:142164651 | C | T | 1 | a0001c0001t0026 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*971G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 971 | chr3 | 142164651 | ||||||
chr3:142164792 | G | C | 1 | a0001c0001t0076 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 830 | chr3 | 142164792 | ||||||
chr3:142165043 | T | C | 3 | a0001c0001t0024 a0001c0001t0069 a0001c0001t0070 |
4 | HG01516.hp1 HG01517.hp2 HG02145.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*579A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 579 | chr3 | 142165043 | ||||||
chr3:142165166 | T | A | 1 | a0001c0001t0071 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 456 | chr3 | 142165166 | ||||||
chr3:142165457 | GT | G | 8 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0023 others(5): Show |
30 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*164delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 164 | chr3 | 142165457 | ||||||
chr3:142165504 | T | C | 1 | a0001c0001t0012 | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*118A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 118 | chr3 | 142165504 | ||||||
chr3:142225502 | C | A | 1 | a0001c0001t0077 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | 47 | chr3 | 142225502 | ||||||
chr3:142225524 | G | C | 1 | a0001c0001t0024 | 2 | HG01516.hp1 HG01517.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-69C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | chr3 | 142225524 | |||||||
chr3:142225529 | C | T | 1 | a0001c0001t0025 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | 74 | chr3 | 142225529 | ||||||
chr3:142225549 | C | A | 1 | a0001c0001t0078 | 1 | HG00741.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | 94 | chr3 | 142225549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142165966 | T | C | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1442-196A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142165966 | |||||||
chr3:142166005 | C | T | 10 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0028 others(7): Show |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1442-235G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166005 | |||||||
chr3:142166270 | A | G | 10 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0028 others(7): Show |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1442-500T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166270 | |||||||
chr3:142166288 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0195 a0001c0001t0001g0197 others(1): Show |
4 | HG01192.hp2 HG01361.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1442-518C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166288 | |||||||
chr3:142166303 | T | C | 1 | a0002c0005t0017g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1442-533A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166303 | |||||||
chr3:142166646 | G | GC | 41 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0019 others(38): Show |
42 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1442-877dupG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166646 | |||||||
chr3:142166659 | G | A | 1 | a0001c0001t0043g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1442-889C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166659 | |||||||
chr3:142166694 | C | T | 1 | a0001c0001t0012g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1442-924G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166694 | |||||||
chr3:142166814 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0019 others(123): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1442-1044A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166814 | |||||||
chr3:142166824 | A | G | 1 | a0001c0001t0068g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1442-1054T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166824 | |||||||
chr3:142167278 | G | A | 30 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(27): Show |
30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1442-1508C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167278 | |||||||
chr3:142167305 | C | T | 1 | a0003c0004t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1442-1535G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167305 | |||||||
chr3:142167384 | A | T | 1 | a0001c0001t0003g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1442-1614T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167384 | |||||||
chr3:142167385 | A | T | 126 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0019 others(123): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1442-1615T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167385 | |||||||
chr3:142167390 | T | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0019 others(123): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1442-1620A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167390 | |||||||
chr3:142167659 | C | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0060 |
4 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1442-1889G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167659 | |||||||
chr3:142167756 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1442-1986C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167756 | |||||||
chr3:142167926 | C | T | 10 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0028 others(7): Show |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1442-2156G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167926 | |||||||
chr3:142167973 | T | C | 1 | a0001c0001t0009g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1442-2203A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167973 | |||||||
chr3:142167979 | T | C | 1 | a0001c0001t0020g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1442-2209A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167979 | |||||||
chr3:142168011 | C | CAAACA | 31 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(28): Show |
31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-2246_1442-224 others(9): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168011 | |||||||
chr3:142168011 | C | CAAACAAA others(3): Show |
1 | a0001c0001t0032g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1442-2251_1442-224 others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168011 | |||||||
chr3:142168081 | G | A | 12 | a0001c0001t0006g0119 a0001c0001t0077g0256 a0001c0002t0006g0218 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1441+2244C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168081 | |||||||
chr3:142168101 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0134 |
2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1441+2224A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168101 | |||||||
chr3:142168109 | T | C | 1 | a0001c0002t0049g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1441+2216A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168109 | |||||||
chr3:142168143 | A | C | 4 | a0001c0001t0018g0034 a0001c0001t0018g0163 a0001c0001t0019g0114 others(1): Show |
4 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441+2182T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168143 | |||||||
chr3:142168469 | A | G | 2 | a0001c0001t0023g0097 a0001c0001t0023g0116 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1441+1856T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168469 | |||||||
chr3:142168644 | C | T | 31 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(28): Show |
31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1441+1681G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168644 | |||||||
chr3:142168679 | T | C | 1 | a0001c0001t0068g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1441+1646A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168679 | |||||||
chr3:142168682 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0080 |
3 | HG00642.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1441+1643A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168682 | |||||||
chr3:142168733 | C | A | 1 | a0001c0001t0076g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1441+1592G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168733 | |||||||
chr3:142168739 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1441+1586G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168739 | |||||||
chr3:142168900 | T | A | 3 | a0001c0001t0030g0153 a0001c0001t0032g0232 a0001c0001t0033g0154 |
3 | HG02145.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1441+1425A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168900 | |||||||
chr3:142168904 | A | G | 27 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(24): Show |
27 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1441+1421T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168904 | |||||||
chr3:142168986 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1441+1339G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168986 | |||||||
chr3:142169067 | G | T | 3 | a0001c0001t0030g0153 a0001c0001t0032g0232 a0001c0001t0033g0154 |
3 | HG02145.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1441+1258C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169067 | |||||||
chr3:142169161 | C | T | 41 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(38): Show |
44 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1441+1164G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169161 | |||||||
chr3:142169236 | C | T | 1 | a0001c0001t0045g0095 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1441+1089G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169236 | |||||||
chr3:142169306 | T | C | 32 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(29): Show |
32 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1441+1019A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169306 | |||||||
chr3:142169555 | T | C | 1 | a0001c0001t0075g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1441+770A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169555 | |||||||
chr3:142169669 | C | CT | 60 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0019 others(57): Show |
64 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1441+655dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169669 | |||||||
chr3:142169669 | C | CTTT | 7 | a0001c0001t0007g0089 a0001c0001t0007g0162 a0001c0001t0007g0213 others(4): Show |
7 | HG01109.hp1 HG01433.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441+653_1441+655d others(5): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169669 | |||||||
chr3:142169669 | CT | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0056 a0001c0001t0018g0034 others(6): Show |
9 | HG01169.hp1 HG01243.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1441+655delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169669 | |||||||
chr3:142169748 | T | A | 1 | a0001c0001t0018g0034 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1441+577A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169748 | |||||||
chr3:142169756 | T | C | 42 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(39): Show |
45 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1441+569A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169756 | |||||||
chr3:142170055 | C | T | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441+270G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170055 | |||||||
chr3:142170167 | T | G | 22 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0019 others(19): Show |
23 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1441+158A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170167 | |||||||
chr3:142170181 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1441+144C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170181 | |||||||
chr3:142170217 | C | T | 1 | a0001c0001t0073g0221 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1441+108G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170217 | |||||||
chr3:142170241 | G | T | 2 | a0001c0001t0020g0137 a0001c0001t0020g0138 |
2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1441+84C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170241 | |||||||
chr3:142170540 | A | G | 12 | a0001c0001t0006g0119 a0001c0001t0077g0256 a0001c0002t0006g0218 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1308-82T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170540 | |||||||
chr3:142170633 | T | G | 30 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(27): Show |
30 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1308-175A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170633 | |||||||
chr3:142170641 | T | A | 1 | a0001c0001t0074g0222 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1308-183A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170641 | |||||||
chr3:142170756 | A | T | 1 | a0003c0004t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1308-298T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170756 | |||||||
chr3:142170796 | A | ATAGC | 115 | a0001c0001t0001g0063 a0001c0001t0002g0005 a0001c0001t0002g0016 others(112): Show |
119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1308-339_1308-338i others(6): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170796 | |||||||
chr3:142170973 | A | G | 4 | a0001c0001t0013g0238 a0001c0001t0013g0255 a0001c0001t0034g0147 others(1): Show |
4 | HG02647.hp2 HG02965.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307+446T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170973 | |||||||
chr3:142171156 | A | C | 1 | a0001c0001t0008g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1307+263T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171156 | |||||||
chr3:142171246 | T | TA | 59 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(56): Show |
59 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.1307+172dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171246 | |||||||
chr3:142171247 | A | T | 11 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0028 others(8): Show |
14 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1307+172T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171247 | |||||||
chr3:142171265 | T | C | 1 | a0001c0001t0060g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1307+154A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171265 | |||||||
chr3:142171670 | G | A | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248-192C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142171670 | |||||||
chr3:142171749 | C | G | 1 | a0001c0001t0004g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1248-271G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142171749 | |||||||
chr3:142172110 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1247+243T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142172110 | |||||||
chr3:142172123 | A | G | 10 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0028 others(7): Show |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1247+230T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142172123 | |||||||
chr3:142172543 | C | A | 10 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0028 others(7): Show |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144-87G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172543 | |||||||
chr3:142172669 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1144-213A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172669 | |||||||
chr3:142172703 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1144-247A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172703 | |||||||
chr3:142172769 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1144-313G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172769 | |||||||
chr3:142172852 | C | G | 2 | a0001c0001t0001g0121 a0001c0001t0008g0120 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1144-396G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172852 | |||||||
chr3:142173031 | C | T | 1 | a0001c0001t0010g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1144-575G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173031 | |||||||
chr3:142173130 | G | A | 1 | a0001c0001t0068g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144-674C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173130 | |||||||
chr3:142173199 | T | TA | 15 | a0001c0001t0001g0063 a0001c0001t0001g0077 a0001c0001t0001g0080 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1144-744dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173199 | |||||||
chr3:142173199 | TA | T | 33 | a0001c0001t0001g0031 a0001c0001t0003g0036 a0001c0001t0003g0040 others(30): Show |
33 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1144-744delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173199 | |||||||
chr3:142173224 | C | CA | 27 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(24): Show |
27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1144-769dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173224 | |||||||
chr3:142173459 | G | A | 1 | a0001c0001t0068g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144-1003C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173459 | |||||||
chr3:142173485 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0044g0039 |
2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1144-1029G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173485 | |||||||
chr3:142173530 | A | G | 1 | a0001c0001t0007g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1144-1074T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173530 | |||||||
chr3:142173550 | G | A | 6 | a0001c0001t0007g0089 a0001c0001t0007g0162 a0001c0001t0007g0213 others(3): Show |
6 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-1094C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173550 | |||||||
chr3:142173578 | G | T | 10 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0028 others(7): Show |
13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144-1122C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173578 | |||||||
chr3:142173609 | G | A | 7 | a0001c0001t0007g0089 a0001c0001t0007g0162 a0001c0001t0007g0213 others(4): Show |
7 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-1153C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173609 | |||||||
chr3:142173615 | C | T | 3 | a0001c0001t0003g0152 a0001c0001t0003g0211 a0001c0001t0003g0212 |
3 | HG01255.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1144-1159G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173615 | |||||||
chr3:142173632 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1144-1176C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173632 | |||||||
chr3:142173683 | C | CAAAACA | 37 | a0001c0001t0001g0063 a0001c0001t0001g0244 a0001c0001t0002g0005 others(34): Show |
38 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.1144-1233_1144-122 others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | |||||||
chr3:142173683 | C | CAAAACAA others(5): Show |
1 | a0001c0001t0002g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1144-1239_1144-122 others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | |||||||
chr3:142173683 | C | CAAAACAA others(11): Show |
1 | a0001c0001t0068g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144-1245_1144-122 others(22): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | |||||||
chr3:142173683 | CAAAACA | C | 54 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(51): Show |
57 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1144-1233_1144-122 others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | |||||||
chr3:142173743 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0008g0120 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1144-1287C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173743 | |||||||
chr3:142173805 | T | C | 42 | a0001c0001t0003g0036 a0001c0001t0003g0040 a0001c0001t0003g0043 others(39): Show |
45 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1144-1349A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173805 | |||||||
chr3:142173834 | G | A | 27 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(24): Show |
27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1144-1378C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173834 | |||||||
chr3:142173911 | C | T | 2 | a0001c0001t0025g0013 a0001c0001t0050g0227 |
2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1144-1455G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173911 | |||||||
chr3:142173968 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1144-1512C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173968 | |||||||
chr3:142174126 | C | G | 28 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(25): Show |
28 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1144-1670G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174126 | |||||||
chr3:142174214 | T | C | 1 | a0001c0001t0001g0001 | 3 | HG02559.hp2 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1144-1758A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174214 | |||||||
chr3:142174386 | G | A | 5 | a0001c0001t0003g0152 a0001c0001t0003g0211 a0001c0001t0003g0212 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-1930C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174386 | |||||||
chr3:142174665 | A | G | 1 | a0001c0001t0075g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1144-2209T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174665 | |||||||
chr3:142174725 | TC | T | 4 | a0001c0001t0003g0061 a0001c0001t0006g0119 a0001c0002t0006g0251 others(1): Show |
4 | HG01884.hp1 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-2270delG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174725 | |||||||
chr3:142174922 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0019g0158 others(1): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1144-2466A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174922 | |||||||
chr3:142175059 | G | A | 108 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0025 others(105): Show |
109 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.1143+2423C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175059 | |||||||
chr3:142175191 | T | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(86): Show |
90 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.1143+2291A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175191 | |||||||
chr3:142175414 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1143+2068G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175414 | |||||||
chr3:142175588 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(127): Show |
132 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(129): Show |
intron_variant | MODIFIER | c.1143+1894G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175588 | |||||||
chr3:142175837 | TATTATTA others(13): Show |
T | 2 | a0001c0001t0010g0207 a0001c0001t0010g0208 |
2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1143+1625_1143+164 others(24): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175837 | |||||||
chr3:142175854 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1143+1628A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175854 | |||||||
chr3:142176047 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0169 |
2 | NA18950.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1143+1435A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176047 | |||||||
chr3:142176074 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1143+1408T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176074 | |||||||
chr3:142176131 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1143+1351A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176131 | |||||||
chr3:142176208 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0122 |
2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1143+1274T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176208 | |||||||
chr3:142176333 | G | C | 43 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(40): Show |
43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1143+1149C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176333 | |||||||
chr3:142176337 | A | C | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1143+1145T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176337 | |||||||
chr3:142176345 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1143+1137C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176345 | |||||||
chr3:142176352 | A | G | 2 | a0001c0001t0010g0041 a0001c0001t0029g0042 |
2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1143+1130T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176352 | |||||||
chr3:142176361 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1143+1121A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176361 | |||||||
chr3:142176402 | G | T | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1143+1080C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176402 | |||||||
chr3:142176497 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1143+985T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176497 | |||||||
chr3:142176607 | T | G | 1 | a0001c0002t0031g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1143+875A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176607 | |||||||
chr3:142176658 | A | AT | 28 | a0001c0001t0001g0134 a0001c0001t0001g0181 a0001c0001t0001g0191 others(25): Show |
28 | HG00621.hp2 HG00741.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143+823dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176658 | |||||||
chr3:142176658 | AT | A | 22 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0003g0043 others(19): Show |
22 | HG01168.hp1 HG01433.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1143+823delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176658 | |||||||
chr3:142176725 | C | CATG | 145 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(142): Show |
147 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.1143+756_1143+757i others(5): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176725 | |||||||
chr3:142176731 | G | A | 11 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0127 others(8): Show |
11 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1143+751C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176731 | |||||||
chr3:142176736 | A | C | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1143+746T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176736 | |||||||
chr3:142176766 | A | G | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1143+716T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176766 | |||||||
chr3:142176770 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0169 |
2 | NA18950.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1143+712A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176770 | |||||||
chr3:142176879 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1143+603A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176879 | |||||||
chr3:142176953 | G | A | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1143+529C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176953 | |||||||
chr3:142177088 | A | G | 1 | a0001c0002t0003g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1143+394T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142177088 | |||||||
chr3:142177268 | A | G | 2 | a0001c0001t0021g0049 a0001c0001t0021g0050 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1143+214T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142177268 | |||||||
chr3:142177476 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01106.hp2 | splice_region_variant&intron_variant | LOW | c.1143+6T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142177476 | |||||||
chr3:142177680 | T | A | 43 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(40): Show |
43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1049-104A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177680 | |||||||
chr3:142177690 | T | C | 43 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(40): Show |
43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1049-114A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177690 | |||||||
chr3:142177711 | C | T | 16 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1049-135G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177711 | |||||||
chr3:142177787 | T | C | 2 | a0001c0001t0043g0239 a0001c0001t0073g0221 |
2 | HG03471.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1049-211A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177787 | |||||||
chr3:142177791 | A | T | 16 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1049-215T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177791 | |||||||
chr3:142177831 | T | C | 10 | a0001c0001t0001g0063 a0001c0001t0001g0253 a0001c0001t0001g0254 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-255A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177831 | |||||||
chr3:142177842 | A | C | 145 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(142): Show |
147 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.1049-266T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177842 | |||||||
chr3:142177855 | T | G | 1 | a0001c0002t0015g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1049-279A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177855 | |||||||
chr3:142177857 | C | CT | 6 | a0001c0001t0001g0204 a0001c0001t0004g0028 a0001c0001t0006g0119 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-282dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177857 | |||||||
chr3:142177857 | CT | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(56): Show |
60 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.1049-282delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177857 | |||||||
chr3:142177867 | T | C | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1049-291A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177867 | |||||||
chr3:142178016 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1049-440C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178016 | |||||||
chr3:142178044 | G | A | 1 | a0001c0001t0060g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1049-468C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178044 | |||||||
chr3:142178137 | C | T | 104 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(101): Show |
105 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(102): Show |
intron_variant | MODIFIER | c.1049-561G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178137 | |||||||
chr3:142178140 | G | T | 43 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(40): Show |
43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1049-564C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178140 | |||||||
chr3:142178144 | C | T | 2 | a0001c0001t0010g0207 a0001c0001t0010g0208 |
2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1049-568G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178144 | |||||||
chr3:142178160 | T | C | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1049-584A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178160 | |||||||
chr3:142178242 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1049-666T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178242 | |||||||
chr3:142178410 | T | A | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1049-834A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178410 | |||||||
chr3:142178553 | C | T | 1 | a0001c0001t0054g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1049-977G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178553 | |||||||
chr3:142178686 | G | C | 1 | a0001c0001t0067g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1049-1110C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178686 | |||||||
chr3:142178755 | T | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0003g0040 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049-1179A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178755 | |||||||
chr3:142178889 | C | A | 1 | a0001c0001t0068g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1049-1313G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178889 | |||||||
chr3:142179056 | TAAAGTGA others(7): Show |
T | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1049-1494_1049-148 others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179056 | |||||||
chr3:142179502 | C | T | 1 | a0001c0001t0020g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1049-1926G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179502 | |||||||
chr3:142179816 | T | C | 145 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(142): Show |
147 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.1048+1645A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179816 | |||||||
chr3:142179860 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1048+1601G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179860 | |||||||
chr3:142180135 | G | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(36): Show |
40 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1048+1326C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180135 | |||||||
chr3:142180138 | T | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(100): Show |
105 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(102): Show |
intron_variant | MODIFIER | c.1048+1323A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180138 | |||||||
chr3:142180269 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048+1192C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180269 | |||||||
chr3:142180306 | TC | T | 5 | a0001c0002t0015g0187 a0001c0002t0015g0189 a0001c0002t0015g0216 others(2): Show |
5 | HG03704.hp2 HG04228.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+1154delG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180306 | |||||||
chr3:142180307 | C | CT | 6 | a0001c0001t0002g0072 a0001c0001t0003g0152 a0001c0001t0023g0116 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048+1153dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180307 | |||||||
chr3:142180372 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0090 |
3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1048+1089C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180372 | |||||||
chr3:142180451 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1048+1010G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180451 | |||||||
chr3:142180464 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1048+997C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180464 | |||||||
chr3:142180494 | G | C | 8 | a0001c0001t0001g0020 a0001c0001t0002g0016 a0001c0001t0002g0019 others(5): Show |
8 | HG02040.hp1 HG02071.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048+967C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180494 | |||||||
chr3:142180521 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1048+940G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180521 | |||||||
chr3:142180764 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1048+697T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180764 | |||||||
chr3:142180819 | G | A | 6 | a0001c0001t0001g0106 a0001c0001t0009g0033 a0001c0001t0009g0108 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048+642C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180819 | |||||||
chr3:142180917 | G | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0075 others(1): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+544C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180917 | |||||||
chr3:142181190 | C | G | 1 | a0001c0001t0011g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1048+271G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181190 | |||||||
chr3:142181207 | G | A | 1 | a0001c0001t0074g0222 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1048+254C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181207 | |||||||
chr3:142181211 | A | G | 2 | a0001c0001t0003g0212 a0001c0001t0007g0089 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1048+250T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181211 | |||||||
chr3:142181328 | T | C | 1 | a0001c0001t0043g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1048+133A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181328 | |||||||
chr3:142181412 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1048+49A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181412 | |||||||
chr3:142181585 | A | C | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.944-20T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181585 | |||||||
chr3:142181782 | T | C | 1 | a0001c0001t0023g0097 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.944-217A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181782 | |||||||
chr3:142181886 | G | A | 13 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0127 others(10): Show |
13 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.944-321C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181886 | |||||||
chr3:142181925 | T | C | 17 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0003g0040 others(14): Show |
17 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.944-360A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181925 | |||||||
chr3:142182128 | C | T | 7 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0113 others(4): Show |
7 | HG01099.hp1 HG01106.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.944-563G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182128 | |||||||
chr3:142182350 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0003g0152 a0001c0001t0023g0116 |
2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.943+562_943+572dup others(11): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182350 | |||||||
chr3:142182406 | G | A | 1 | a0001c0001t0032g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943+517C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182406 | |||||||
chr3:142182569 | G | C | 1 | a0001c0001t0074g0222 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.943+354C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182569 | |||||||
chr3:142183106 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0008g0120 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.817-57A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183106 | |||||||
chr3:142183232 | C | T | 31 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(28): Show |
32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.817-183G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183232 | |||||||
chr3:142183420 | A | G | 2 | a0001c0001t0002g0165 a0001c0001t0004g0166 |
2 | NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.817-371T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183420 | |||||||
chr3:142183422 | T | C | 1 | a0001c0001t0005g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.817-373A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183422 | |||||||
chr3:142183435 | A | G | 1 | a0001c0002t0049g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.817-386T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183435 | |||||||
chr3:142183658 | A | G | 12 | a0001c0002t0003g0242 a0001c0002t0006g0218 a0001c0002t0006g0219 others(9): Show |
12 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.817-609T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183658 | |||||||
chr3:142183778 | T | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(28): Show |
32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.817-729A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183778 | |||||||
chr3:142183819 | A | C | 1 | a0001c0001t0033g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.817-770T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183819 | |||||||
chr3:142183996 | C | T | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.817-947G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183996 | |||||||
chr3:142183997 | G | A | 1 | a0001c0001t0067g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.817-948C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183997 | |||||||
chr3:142184046 | C | T | 2 | a0001c0001t0013g0238 a0001c0001t0013g0255 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.817-997G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184046 | |||||||
chr3:142184086 | A | G | 5 | a0001c0002t0006g0218 a0001c0002t0006g0219 a0001c0002t0006g0220 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-1037T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184086 | |||||||
chr3:142184131 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0002t0003g0242 others(11): Show |
15 | HG02280.hp2 HG02559.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.817-1082C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184131 | |||||||
chr3:142184198 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.817-1149A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184198 | |||||||
chr3:142184260 | C | CA | 26 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0240 others(23): Show |
27 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.817-1212dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAA | 6 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0127 others(3): Show |
6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-1213_817-1212d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAA | 13 | a0001c0001t0001g0102 a0001c0001t0002g0019 a0001c0001t0030g0153 others(10): Show |
13 | HG02559.hp1 HG02809.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-1214_817-1212d others(5): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAAA | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(50): Show |
55 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.817-1215_817-1212d others(6): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAAAA | 30 | a0001c0001t0001g0015 a0001c0001t0001g0090 a0001c0001t0001g0100 others(27): Show |
30 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.817-1216_817-1212d others(7): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0016g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.817-1222_817-1212d others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0005g0145 a0001c0001t0034g0147 a0001c0001t0040g0144 |
3 | HG02630.hp1 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.817-1223_817-1212d others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0146 others(2): Show |
5 | HG01891.hp2 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-1224_817-1212d others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0005g0142 a0001c0001t0035g0115 a0001c0001t0036g0037 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-1225_817-1212d others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184260 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0038g0143 a0001c0001t0039g0150 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.817-1226_817-1212d others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | |||||||
chr3:142184275 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.817-1226T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184275 | |||||||
chr3:142184578 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.816+1351G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184578 | |||||||
chr3:142184663 | C | T | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.816+1266G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184663 | |||||||
chr3:142184956 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.816+973C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184956 | |||||||
chr3:142185063 | C | A | 146 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(143): Show |
148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.816+866G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185063 | |||||||
chr3:142185145 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(143): Show |
148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.816+784T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185145 | |||||||
chr3:142185150 | T | A | 11 | a0001c0001t0001g0230 a0001c0001t0003g0211 a0001c0001t0003g0212 others(8): Show |
11 | HG01175.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+779A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185150 | |||||||
chr3:142185345 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.816+584G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185345 | |||||||
chr3:142185412 | CA | C | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(120): Show |
125 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(122): Show |
intron_variant | MODIFIER | c.816+516delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185412 | |||||||
chr3:142185412 | CAA | C | 22 | a0001c0001t0001g0063 a0001c0001t0001g0100 a0001c0001t0001g0122 others(19): Show |
22 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.816+515_816+516del others(2): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185412 | |||||||
chr3:142185413 | A | G | 1 | a0001c0001t0022g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.816+516T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185413 | |||||||
chr3:142185632 | C | T | 146 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(143): Show |
148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.816+297G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185632 | |||||||
chr3:142185689 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0090 |
3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+240C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185689 | |||||||
chr3:142186080 | G | C | 10 | a0001c0001t0006g0119 a0001c0001t0011g0092 a0001c0001t0011g0094 others(7): Show |
10 | HG00738.hp1 HG01123.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.756-91C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 8/15 | chr3 | 142186080 | |||||||
chr3:142186130 | C | T | 1 | a0001c0002t0015g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.755+64G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 8/15 | chr3 | 142186130 | |||||||
chr3:142186135 | G | A | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.755+59C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 8/15 | chr3 | 142186135 | |||||||
chr3:142186339 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.682-72A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186339 | |||||||
chr3:142186411 | C | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(44): Show |
48 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.681+41G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186411 | |||||||
chr3:142186417 | T | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(44): Show |
48 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.681+35A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186417 | |||||||
chr3:142186419 | T | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(44): Show |
48 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.681+33A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186419 | |||||||
chr3:142186435 | GA | G | 13 | a0001c0001t0001g0156 a0001c0002t0003g0242 a0001c0002t0006g0218 others(10): Show |
13 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.681+16delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186435 | |||||||
chr3:142186444 | A | T | 1 | a0001c0001t0043g0239 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.681+8T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186444 | |||||||
chr3:142186572 | G | A | 3 | a0001c0001t0005g0030 a0001c0001t0036g0037 a0001c0001t0037g0038 |
3 | HG02486.hp1 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.620-59C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186572 | |||||||
chr3:142186630 | C | CT | 19 | a0001c0001t0001g0063 a0001c0001t0001g0075 a0001c0001t0001g0197 others(16): Show |
19 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.620-118dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186630 | |||||||
chr3:142186630 | CT | C | 8 | a0001c0001t0001g0088 a0001c0001t0001g0122 a0001c0001t0001g0130 others(5): Show |
8 | HG01257.hp1 HG02486.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.620-118delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186630 | |||||||
chr3:142186632 | T | C | 1 | a0001c0001t0004g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.620-119A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186632 | |||||||
chr3:142186769 | T | G | 80 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(77): Show |
81 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.620-256A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186769 | |||||||
chr3:142186778 | G | A | 6 | a0001c0001t0001g0106 a0001c0001t0009g0033 a0001c0001t0009g0108 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.620-265C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186778 | |||||||
chr3:142186788 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(143): Show |
148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.620-275T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186788 | |||||||
chr3:142186863 | T | C | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.620-350A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186863 | |||||||
chr3:142187042 | C | T | 1 | a0001c0001t0039g0150 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620-529G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187042 | |||||||
chr3:142187341 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.619+363G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187341 | |||||||
chr3:142187555 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0008g0120 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.619+149A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187555 | |||||||
chr3:142187575 | C | A | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.619+129G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187575 | |||||||
chr3:142187604 | C | CA | 15 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0128 others(12): Show |
15 | HG01175.hp1 HG01358.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.619+99dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187604 | |||||||
chr3:142187604 | CA | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0063 others(12): Show |
16 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.619+99delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187604 | |||||||
chr3:142187996 | A | G | 1 | a0002c0005t0017g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.544-217T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142187996 | |||||||
chr3:142188032 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-253G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188032 | |||||||
chr3:142188125 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.544-346C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188125 | |||||||
chr3:142188163 | G | A | 42 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(39): Show |
42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.544-384C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188163 | |||||||
chr3:142188300 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.544-521C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188300 | |||||||
chr3:142188322 | G | C | 1 | a0001c0001t0003g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.544-543C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188322 | |||||||
chr3:142188342 | T | C | 1 | a0001c0001t0033g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-563A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188342 | |||||||
chr3:142188357 | C | T | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-578G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188357 | |||||||
chr3:142188464 | G | A | 18 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-685C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188464 | |||||||
chr3:142188541 | C | CA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0102 a0001c0001t0001g0104 others(3): Show |
7 | HG04115.hp2 NA18941.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-763dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188541 | |||||||
chr3:142188561 | G | C | 18 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-782C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188561 | |||||||
chr3:142188627 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-848T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188627 | |||||||
chr3:142188734 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.544-955C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188734 | |||||||
chr3:142188835 | C | T | 2 | a0001c0001t0041g0140 a0001c0001t0042g0139 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-1056G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188835 | |||||||
chr3:142188837 | A | G | 13 | a0001c0001t0001g0156 a0001c0002t0003g0242 a0001c0002t0006g0218 others(10): Show |
13 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.544-1058T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188837 | |||||||
chr3:142189724 | C | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0005g0210 others(3): Show |
6 | HG01255.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1945G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142189724 | |||||||
chr3:142190161 | G | A | 3 | a0001c0001t0005g0030 a0001c0001t0036g0037 a0001c0001t0037g0038 |
3 | HG02486.hp1 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.544-2382C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190161 | |||||||
chr3:142190319 | C | T | 5 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0127 others(2): Show |
5 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-2540G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190319 | |||||||
chr3:142190331 | A | G | 20 | a0001c0001t0001g0063 a0001c0001t0001g0122 a0001c0001t0003g0061 others(17): Show |
20 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.544-2552T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190331 | |||||||
chr3:142190351 | C | T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(39): Show |
42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.544-2572G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190351 | |||||||
chr3:142190455 | C | A | 1 | a0001c0001t0057g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.544-2676G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190455 | |||||||
chr3:142190639 | A | C | 145 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(142): Show |
146 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(143): Show |
intron_variant | MODIFIER | c.544-2860T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190639 | |||||||
chr3:142190713 | T | C | 1 | a0001c0001t0032g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-2934A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190713 | |||||||
chr3:142191002 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-3223T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191002 | |||||||
chr3:142191048 | AT | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(47): Show |
51 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.544-3270delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191048 | |||||||
chr3:142191189 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.544-3410G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191189 | |||||||
chr3:142191319 | C | T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(39): Show |
42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.544-3540G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191319 | |||||||
chr3:142191870 | G | A | 2 | a0001c0001t0041g0140 a0001c0001t0042g0139 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-4091C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191870 | |||||||
chr3:142191899 | G | A | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-4120C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191899 | |||||||
chr3:142192095 | T | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(28): Show |
32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.544-4316A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192095 | |||||||
chr3:142192564 | G | C | 13 | a0001c0001t0001g0156 a0001c0002t0003g0242 a0001c0002t0006g0218 others(10): Show |
13 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.544-4785C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192564 | |||||||
chr3:142192570 | C | G | 3 | a0001c0001t0005g0030 a0001c0001t0036g0037 a0001c0001t0037g0038 |
3 | HG02486.hp1 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.544-4791G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192570 | |||||||
chr3:142192589 | T | C | 144 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(141): Show |
145 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(142): Show |
intron_variant | MODIFIER | c.544-4810A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192589 | |||||||
chr3:142192590 | C | T | 1 | a0001c0001t0023g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-4811G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192590 | |||||||
chr3:142192664 | T | C | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-4885A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192664 | |||||||
chr3:142192758 | T | C | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-4979A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192758 | |||||||
chr3:142192763 | C | CA | 14 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0113 others(11): Show |
14 | HG01099.hp1 HG01106.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-4985dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192763 | |||||||
chr3:142192763 | C | CAA | 18 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-4986_544-4985d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192763 | |||||||
chr3:142192763 | CA | C | 6 | a0001c0001t0003g0059 a0001c0001t0041g0140 a0001c0001t0042g0139 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-4985delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192763 | |||||||
chr3:142193086 | T | G | 1 | a0002c0005t0017g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.544-5307A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193086 | |||||||
chr3:142193261 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.544-5482T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193261 | |||||||
chr3:142193483 | C | CA | 33 | a0001c0001t0001g0071 a0001c0001t0001g0169 a0001c0001t0001g0240 others(30): Show |
33 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.543+5318dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193483 | |||||||
chr3:142193489 | A | C | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+5313T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193489 | |||||||
chr3:142193708 | T | C | 2 | a0001c0001t0003g0036 a0001c0001t0026g0035 |
2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.543+5094A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193708 | |||||||
chr3:142193793 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+5009A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193793 | |||||||
chr3:142193929 | C | T | 11 | a0001c0001t0001g0230 a0001c0001t0003g0211 a0001c0001t0003g0212 others(8): Show |
11 | HG01175.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+4873G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193929 | |||||||
chr3:142193983 | C | T | 1 | a0001c0002t0031g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543+4819G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193983 | |||||||
chr3:142194127 | G | C | 1 | a0001c0001t0003g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+4675C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194127 | |||||||
chr3:142194394 | C | T | 12 | a0001c0001t0001g0122 a0001c0001t0003g0061 a0001c0001t0003g0062 others(9): Show |
12 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+4408G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194394 | |||||||
chr3:142194489 | GC | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(8): Show |
11 | HG00642.hp1 HG02040.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+4312delG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194489 | |||||||
chr3:142194525 | C | T | 1 | a0001c0001t0053g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+4277G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194525 | |||||||
chr3:142194527 | A | G | 1 | a0001c0002t0003g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.543+4275T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194527 | |||||||
chr3:142194634 | T | A | 1 | a0001c0001t0017g0149 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.543+4168A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194634 | |||||||
chr3:142194694 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.543+4108T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194694 | |||||||
chr3:142194724 | T | C | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+4078A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194724 | |||||||
chr3:142194729 | C | G | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+4073G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194729 | |||||||
chr3:142194974 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.543+3828G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194974 | |||||||
chr3:142195151 | T | C | 63 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(60): Show |
64 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.543+3651A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195151 | |||||||
chr3:142195314 | C | T | 1 | a0001c0001t0071g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.543+3488G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195314 | |||||||
chr3:142195325 | T | G | 11 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0127 others(8): Show |
11 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+3477A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195325 | |||||||
chr3:142195612 | A | G | 1 | a0002c0005t0017g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.543+3190T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195612 | |||||||
chr3:142195654 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+3148C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195654 | |||||||
chr3:142195744 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
14 | HG01175.hp1 HG01192.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+3058A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195744 | |||||||
chr3:142196172 | A | G | 12 | a0001c0001t0001g0122 a0001c0001t0003g0061 a0001c0001t0003g0062 others(9): Show |
12 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+2630T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196172 | |||||||
chr3:142196514 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.543+2288A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196514 | |||||||
chr3:142196573 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.543+2229G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196573 | |||||||
chr3:142196678 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.543+2124G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196678 | |||||||
chr3:142196723 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0090 |
3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.543+2079A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196723 | |||||||
chr3:142197079 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.543+1723G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197079 | |||||||
chr3:142197236 | T | C | 1 | a0001c0001t0039g0150 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+1566A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197236 | |||||||
chr3:142197350 | C | G | 2 | a0001c0001t0041g0140 a0001c0001t0042g0139 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.543+1452G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197350 | |||||||
chr3:142197413 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
138 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(135): Show |
intron_variant | MODIFIER | c.543+1389G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197413 | |||||||
chr3:142197818 | T | C | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.543+984A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197818 | |||||||
chr3:142197820 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0008g0120 a0001c0001t0042g0139 |
3 | HG02056.hp1 HG02165.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.543+982G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197820 | |||||||
chr3:142197868 | C | G | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.543+934G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197868 | |||||||
chr3:142197978 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(22): Show |
26 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.543+824C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197978 | |||||||
chr3:142198036 | A | T | 8 | a0001c0001t0001g0063 a0001c0001t0010g0041 a0001c0001t0010g0125 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+766T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198036 | |||||||
chr3:142198058 | T | C | 2 | a0001c0001t0007g0215 a0001c0001t0007g0231 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.543+744A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198058 | |||||||
chr3:142198253 | T | C | 1 | a0001c0001t0032g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+549A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198253 | |||||||
chr3:142198340 | T | C | 1 | a0001c0002t0006g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.543+462A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198340 | |||||||
chr3:142198343 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
138 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(135): Show |
intron_variant | MODIFIER | c.543+459G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198343 | |||||||
chr3:142198441 | C | T | 12 | a0001c0001t0001g0122 a0001c0001t0003g0061 a0001c0001t0003g0062 others(9): Show |
12 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+361G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198441 | |||||||
chr3:142198714 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0054g0103 |
4 | NA18956.hp2 NA18982.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+88A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198714 | |||||||
chr3:142198790 | G | A | 1 | a0001c0001t0007g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.543+12C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198790 | |||||||
chr3:142198968 | T | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(28): Show |
32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.412-35A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142198968 | |||||||
chr3:142198983 | A | G | 1 | a0001c0001t0014g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.412-50T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142198983 | |||||||
chr3:142199009 | G | T | 1 | a0001c0001t0043g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-76C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199009 | |||||||
chr3:142199124 | A | G | 1 | a0001c0001t0043g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-191T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199124 | |||||||
chr3:142199192 | T | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0240 others(2): Show |
6 | HG02280.hp2 HG02486.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-259A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199192 | |||||||
chr3:142199225 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.412-292G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199225 | |||||||
chr3:142199601 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.412-668A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199601 | |||||||
chr3:142199625 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.412-692T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199625 | |||||||
chr3:142199857 | A | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.412-924T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199857 | |||||||
chr3:142199864 | T | C | 42 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(39): Show |
42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.412-931A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199864 | |||||||
chr3:142200087 | CTA | C | 3 | a0001c0001t0003g0047 a0001c0001t0032g0232 a0001c0001t0078g0257 |
3 | HG00741.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.412-1156_412-1155d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200087 | |||||||
chr3:142200096 | T | C | 6 | a0001c0001t0001g0063 a0001c0001t0010g0041 a0001c0001t0010g0125 others(3): Show |
6 | HG00099.hp1 HG00642.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-1163A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200096 | |||||||
chr3:142200098 | T | C | 23 | a0001c0001t0001g0063 a0001c0001t0001g0122 a0001c0001t0002g0072 others(20): Show |
23 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.412-1165A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | |||||||
chr3:142200098 | T | TAC | 11 | a0001c0001t0001g0105 a0001c0001t0001g0156 a0001c0001t0041g0140 others(8): Show |
11 | HG01099.hp1 HG02602.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.412-1167_412-1166d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | |||||||
chr3:142200098 | T | TACACAC | 17 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0142 others(14): Show |
17 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.412-1171_412-1166d others(8): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | |||||||
chr3:142200098 | TACAC | T | 3 | a0001c0001t0001g0240 a0001c0001t0003g0152 a0001c0001t0023g0116 |
3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.412-1169_412-1166d others(6): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | |||||||
chr3:142200100 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.412-1167G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200100 | |||||||
chr3:142200245 | T | C | 1 | a0001c0001t0011g0092 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.412-1312A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200245 | |||||||
chr3:142200610 | C | T | 5 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-1677G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200610 | |||||||
chr3:142200668 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.412-1735G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200668 | |||||||
chr3:142200769 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.412-1836T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200769 | |||||||
chr3:142201089 | C | T | 41 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(38): Show |
41 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.412-2156G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201089 | |||||||
chr3:142201192 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.412-2259A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201192 | |||||||
chr3:142201231 | T | C | 17 | a0001c0001t0001g0156 a0001c0001t0001g0230 a0001c0001t0002g0072 others(14): Show |
17 | HG01175.hp2 HG02559.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.412-2298A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201231 | |||||||
chr3:142201278 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.412-2345A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201278 | |||||||
chr3:142201426 | A | C | 4 | a0001c0001t0005g0030 a0001c0001t0018g0034 a0001c0001t0036g0037 others(1): Show |
4 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-2493T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201426 | |||||||
chr3:142201592 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
172 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.412-2659C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201592 | |||||||
chr3:142201614 | A | C | 1 | a0001c0001t0022g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.412-2681T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201614 | |||||||
chr3:142201627 | C | T | 2 | a0001c0001t0002g0067 a0001c0001t0002g0073 |
2 | HG00597.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.412-2694G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201627 | |||||||
chr3:142201631 | T | C | 1 | a0001c0001t0011g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.412-2698A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201631 | |||||||
chr3:142201719 | C | T | 2 | a0001c0001t0013g0238 a0001c0001t0013g0255 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-2786G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201719 | |||||||
chr3:142201723 | G | A | 2 | a0001c0001t0023g0116 a0002c0005t0017g0203 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.412-2790C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201723 | |||||||
chr3:142201725 | C | A | 2 | a0001c0001t0013g0238 a0001c0001t0013g0255 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-2792G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201725 | |||||||
chr3:142201768 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
180 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.412-2835C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201768 | |||||||
chr3:142201997 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(62): Show |
70 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.411+2698C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201997 | |||||||
chr3:142202017 | G | C | 97 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(94): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.411+2678C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142202017 | |||||||
chr3:142202044 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.411+2651G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142202044 | |||||||
chr3:142202743 | G | A | 4 | a0001c0001t0001g0228 a0001c0001t0004g0229 a0001c0001t0025g0013 others(1): Show |
4 | NA18950.hp2 NA18982.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1952C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142202743 | |||||||
chr3:142203300 | T | A | 5 | a0001c0001t0003g0036 a0001c0001t0018g0034 a0001c0001t0026g0035 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1395A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203300 | |||||||
chr3:142203436 | A | C | 1 | a0001c0002t0015g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.411+1259T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203436 | |||||||
chr3:142203444 | A | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.411+1251T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203444 | |||||||
chr3:142203501 | G | A | 1 | a0001c0001t0007g0089 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.411+1194C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203501 | |||||||
chr3:142203568 | A | C | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0005g0210 others(1): Show |
4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1127T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203568 | |||||||
chr3:142203591 | G | A | 15 | a0001c0001t0003g0152 a0001c0001t0005g0029 a0001c0001t0005g0142 others(12): Show |
15 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+1104C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203591 | |||||||
chr3:142203731 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.411+964C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203731 | |||||||
chr3:142203964 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.411+731A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203964 | |||||||
chr3:142203982 | T | C | 3 | a0001c0002t0006g0218 a0001c0002t0006g0219 a0001c0002t0006g0220 |
3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.411+713A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203982 | |||||||
chr3:142204014 | C | T | 1 | a0001c0001t0073g0221 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.411+681G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204014 | |||||||
chr3:142204095 | T | G | 1 | a0001c0001t0008g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.411+600A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204095 | |||||||
chr3:142204200 | T | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.411+495A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204200 | |||||||
chr3:142204335 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0135 |
2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.411+360T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204335 | |||||||
chr3:142204380 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0090 |
3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+315A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204380 | |||||||
chr3:142204526 | C | G | 1 | a0001c0001t0004g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.411+169G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204526 | |||||||
chr3:142204636 | A | T | 1 | a0001c0001t0018g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411+59T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204636 | |||||||
chr3:142204641 | C | T | 3 | a0001c0002t0006g0218 a0001c0002t0006g0219 a0001c0002t0006g0220 |
3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.411+54G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204641 | |||||||
chr3:142204664 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
169 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.411+31G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204664 | |||||||
chr3:142204940 | T | C | 1 | a0001c0001t0018g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318-152A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142204940 | |||||||
chr3:142205277 | A | C | 1 | a0001c0001t0008g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.318-489T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205277 | |||||||
chr3:142205451 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.318-663G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205451 | |||||||
chr3:142205497 | T | A | 15 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0228 others(12): Show |
15 | HG00597.hp1 HG01175.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.318-709A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205497 | |||||||
chr3:142205834 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
200 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.318-1046T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205834 | |||||||
chr3:142206025 | G | C | 1 | a0001c0001t0004g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.318-1237C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206025 | |||||||
chr3:142206027 | T | C | 1 | a0001c0001t0011g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.318-1239A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206027 | |||||||
chr3:142206100 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(128): Show |
140 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.318-1312G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206100 | |||||||
chr3:142206101 | G | A | 1 | a0001c0001t0007g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.318-1313C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206101 | |||||||
chr3:142206189 | C | G | 1 | a0001c0002t0031g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.318-1401G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206189 | |||||||
chr3:142206197 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.318-1409A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206197 | |||||||
chr3:142206289 | T | G | 1 | a0001c0001t0078g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.318-1501A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206289 | |||||||
chr3:142206354 | G | A | 18 | a0001c0001t0001g0122 a0001c0001t0003g0152 a0001c0001t0005g0029 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-1566C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206354 | |||||||
chr3:142206550 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318-1762A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206550 | |||||||
chr3:142206562 | T | C | 15 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0228 others(12): Show |
15 | HG00597.hp1 HG01175.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.318-1774A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206562 | |||||||
chr3:142206590 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.318-1802T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206590 | |||||||
chr3:142206600 | T | C | 3 | a0001c0002t0006g0218 a0001c0002t0006g0219 a0001c0002t0006g0220 |
3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.318-1812A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206600 | |||||||
chr3:142206724 | C | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.318-1936G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206724 | |||||||
chr3:142206921 | T | C | 3 | a0001c0002t0006g0218 a0001c0002t0006g0219 a0001c0002t0006g0220 |
3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.318-2133A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206921 | |||||||
chr3:142207024 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.318-2236A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207024 | |||||||
chr3:142207283 | C | T | 1 | a0001c0001t0053g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.318-2495G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207283 | |||||||
chr3:142207319 | C | T | 1 | a0001c0001t0008g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.318-2531G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207319 | |||||||
chr3:142207432 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.318-2644G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207432 | |||||||
chr3:142207653 | C | G | 3 | a0001c0001t0001g0240 a0001c0001t0007g0233 a0001c0001t0032g0232 |
3 | HG01433.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.318-2865G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207653 | |||||||
chr3:142207676 | C | A | 18 | a0001c0001t0001g0122 a0001c0001t0003g0152 a0001c0001t0005g0029 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-2888G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207676 | |||||||
chr3:142207704 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0100 others(31): Show |
35 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.318-2916C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207704 | |||||||
chr3:142207794 | C | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0100 others(32): Show |
36 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.318-3006G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207794 | |||||||
chr3:142207931 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.318-3143C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207931 | |||||||
chr3:142208244 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0090 |
3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.318-3456C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208244 | |||||||
chr3:142208652 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
84 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.318-3864T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208652 | |||||||
chr3:142208795 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0041g0140 a0001c0001t0042g0139 |
3 | HG02965.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.318-4007C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208795 | |||||||
chr3:142208872 | G | A | 2 | a0001c0001t0007g0215 a0001c0001t0022g0214 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.318-4084C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208872 | |||||||
chr3:142208875 | C | T | 18 | a0001c0001t0001g0122 a0001c0001t0003g0152 a0001c0001t0005g0029 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-4087G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208875 | |||||||
chr3:142208925 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.318-4137C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208925 | |||||||
chr3:142208964 | A | G | 10 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0005g0210 others(7): Show |
10 | HG01255.hp1 HG01891.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-4176T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208964 | |||||||
chr3:142209097 | C | T | 1 | a0001c0001t0072g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.318-4309G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209097 | |||||||
chr3:142209115 | C | T | 1 | a0001c0001t0066g0026 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.318-4327G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209115 | |||||||
chr3:142209144 | G | A | 18 | a0001c0001t0001g0122 a0001c0001t0003g0152 a0001c0001t0005g0029 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-4356C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209144 | |||||||
chr3:142209148 | C | CA | 16 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0228 others(13): Show |
16 | HG00597.hp1 HG01175.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.318-4361dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209148 | |||||||
chr3:142209514 | A | C | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+4012T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209514 | |||||||
chr3:142209552 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.317+3974T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209552 | |||||||
chr3:142209709 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0001g0195 others(6): Show |
10 | HG00408.hp2 HG00621.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+3817A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209709 | |||||||
chr3:142209809 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.317+3717G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209809 | |||||||
chr3:142209897 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.317+3629A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209897 | |||||||
chr3:142209927 | A | T | 5 | a0001c0001t0003g0036 a0001c0001t0018g0034 a0001c0001t0026g0035 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+3599T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209927 | |||||||
chr3:142209951 | A | AT | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.317+3574dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209951 | |||||||
chr3:142210165 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.317+3361G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210165 | |||||||
chr3:142210427 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.317+3099A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210427 | |||||||
chr3:142210850 | C | T | 3 | a0001c0001t0010g0041 a0001c0001t0010g0125 a0001c0001t0029g0042 |
3 | HG03831.hp2 HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.317+2676G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210850 | |||||||
chr3:142210930 | C | CTCCACTT others(7): Show |
15 | a0001c0001t0003g0152 a0001c0001t0005g0029 a0001c0001t0005g0142 others(12): Show |
15 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.317+2582_317+2595d others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210930 | |||||||
chr3:142211020 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): Show |
189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.317+2506T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211020 | |||||||
chr3:142211164 | G | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.317+2362C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211164 | |||||||
chr3:142211464 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.317+2062T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211464 | |||||||
chr3:142211492 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0007g0231 |
2 | HG01175.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.317+2034A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211492 | |||||||
chr3:142211571 | C | A | 1 | a0001c0001t0037g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.317+1955G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211571 | |||||||
chr3:142211594 | A | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): Show |
189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.317+1932T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211594 | |||||||
chr3:142212219 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0044g0039 |
2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.317+1307G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212219 | |||||||
chr3:142212463 | G | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.317+1063C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212463 | |||||||
chr3:142212551 | G | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.317+975C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212551 | |||||||
chr3:142212630 | A | C | 1 | a0001c0001t0007g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.317+896T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212630 | |||||||
chr3:142212707 | T | C | 1 | a0001c0001t0034g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.317+819A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212707 | |||||||
chr3:142212753 | TACTATAC others(4): Show |
T | 2 | a0001c0001t0005g0030 a0001c0001t0043g0239 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.317+762_317+772del others(11): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212753 | |||||||
chr3:142212793 | A | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(176): Show |
188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.317+733T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212793 | |||||||
chr3:142212822 | A | ATGTTTTC others(5): Show |
5 | a0001c0001t0011g0094 a0001c0001t0023g0097 a0001c0001t0045g0095 others(2): Show |
5 | HG00738.hp1 HG01123.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+703_317+704ins others(12): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212822 | |||||||
chr3:142212822 | A | ATGTTTTC others(6): Show |
1 | a0001c0001t0011g0092 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.317+703_317+704ins others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212822 | |||||||
chr3:142212824 | A | ATTTTCTT others(5): Show |
170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(167): Show |
179 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.317+690_317+701dup others(12): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212824 | |||||||
chr3:142212824 | A | G | 1 | a0001c0001t0006g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.317+702T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212824 | |||||||
chr3:142212824 | A | T | 6 | a0001c0001t0011g0092 a0001c0001t0011g0094 a0001c0001t0023g0097 others(3): Show |
6 | HG00738.hp1 HG01123.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+702T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212824 | |||||||
chr3:142212839 | T | TTCTTTTT others(6): Show |
5 | a0001c0001t0001g0134 a0001c0001t0007g0215 a0001c0001t0007g0233 others(2): Show |
5 | HG01433.hp1 HG02074.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+686_317+687ins others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212839 | |||||||
chr3:142212840 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0007g0215 a0001c0001t0022g0214 others(1): Show |
4 | HG02074.hp1 HG02615.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+686G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212840 | |||||||
chr3:142212940 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(176): Show |
188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.317+586A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212940 | |||||||
chr3:142213055 | C | T | 1 | a0002c0005t0017g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.317+471G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213055 | |||||||
chr3:142213056 | G | C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG00438.hp2 HG01123.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+470C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213056 | |||||||
chr3:142213086 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
83 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+440C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213086 | |||||||
chr3:142213126 | T | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): Show |
191 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.317+400A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213126 | |||||||
chr3:142213164 | C | A | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0005g0210 others(1): Show |
4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+362G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213164 | |||||||
chr3:142213283 | CGAAA | C | 5 | a0001c0001t0003g0036 a0001c0001t0018g0034 a0001c0001t0026g0035 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+239_317+242del others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213283 | |||||||
chr3:142213352 | C | G | 1 | a0001c0001t0014g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.317+174G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213352 | |||||||
chr3:142213514 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(176): Show |
188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.317+12C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213514 | |||||||
chr3:142213689 | T | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0100 others(34): Show |
38 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.242-88A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213689 | |||||||
chr3:142213709 | T | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
87 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.242-108A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213709 | |||||||
chr3:142213711 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.242-110C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213711 | |||||||
chr3:142213777 | T | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(53): Show |
57 | HG00738.hp2 HG00741.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.242-176A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213777 | |||||||
chr3:142214326 | G | A | 1 | a0001c0002t0013g0252 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.242-725C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214326 | |||||||
chr3:142214377 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0013g0238 a0001c0001t0013g0255 |
3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.242-776A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214377 | |||||||
chr3:142214459 | G | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.242-858C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214459 | |||||||
chr3:142214807 | C | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
87 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.241+792G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214807 | |||||||
chr3:142214945 | T | C | 14 | a0001c0001t0003g0152 a0001c0001t0005g0029 a0001c0001t0005g0142 others(11): Show |
14 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.241+654A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214945 | |||||||
chr3:142215072 | C | G | 2 | a0001c0001t0002g0165 a0001c0001t0004g0166 |
2 | NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.241+527G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215072 | |||||||
chr3:142215229 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0008g0120 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.241+370C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215229 | |||||||
chr3:142215495 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.241+104T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215495 | |||||||
chr3:142215551 | C | CA | 17 | a0001c0001t0001g0122 a0001c0001t0005g0029 a0001c0001t0005g0142 others(14): Show |
17 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.241+47dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215551 | |||||||
chr3:142216065 | G | A | 2 | a0001c0001t0005g0030 a0001c0001t0043g0239 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.148-373C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216065 | |||||||
chr3:142216552 | T | C | 28 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0228 others(25): Show |
28 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.148-860A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216552 | |||||||
chr3:142216578 | C | T | 6 | a0001c0001t0005g0029 a0001c0001t0011g0148 a0001c0001t0017g0149 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-886G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216578 | |||||||
chr3:142216797 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0013g0238 a0001c0001t0013g0255 |
3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.148-1105A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216797 | |||||||
chr3:142216864 | T | C | 4 | a0001c0001t0005g0029 a0001c0001t0011g0148 a0001c0001t0017g0149 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-1172A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216864 | |||||||
chr3:142217445 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.148-1753C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142217445 | |||||||
chr3:142217590 | G | GA | 6 | a0001c0001t0005g0030 a0001c0001t0012g0234 a0001c0001t0012g0235 others(3): Show |
6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-1899dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142217590 | |||||||
chr3:142217713 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0013g0238 a0001c0001t0013g0255 |
3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.148-2021A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142217713 | |||||||
chr3:142218111 | C | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0135 |
2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.148-2419G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218111 | |||||||
chr3:142218229 | C | CA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0005g0030 others(6): Show |
9 | HG01891.hp1 HG02886.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-2538dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218229 | |||||||
chr3:142218304 | G | A | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-2612C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218304 | |||||||
chr3:142218369 | C | T | 1 | a0001c0001t0009g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.148-2677G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218369 | |||||||
chr3:142218377 | C | CA | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.148-2686dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218377 | |||||||
chr3:142218377 | C | CAA | 28 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0024 others(25): Show |
28 | HG01255.hp1 HG01433.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.148-2687_148-2686d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218377 | |||||||
chr3:142218413 | G | A | 4 | a0001c0001t0014g0131 a0001c0001t0014g0132 a0001c0001t0014g0133 others(1): Show |
4 | HG01074.hp2 HG03710.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-2721C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218413 | |||||||
chr3:142218469 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148-2777T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218469 | |||||||
chr3:142218540 | C | CA | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0205 others(4): Show |
7 | HG02074.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-2849dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218540 | |||||||
chr3:142218735 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148-3043C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218735 | |||||||
chr3:142218744 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.148-3052A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218744 | |||||||
chr3:142218876 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0010g0207 a0001c0001t0010g0208 |
3 | HG00099.hp1 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.148-3184A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218876 | |||||||
chr3:142219038 | A | G | 2 | a0001c0001t0007g0215 a0001c0001t0022g0214 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.148-3346T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219038 | |||||||
chr3:142219111 | T | C | 28 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0228 others(25): Show |
28 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.148-3419A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219111 | |||||||
chr3:142219650 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148-3958A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219650 | |||||||
chr3:142219889 | A | C | 1 | a0001c0001t0058g0032 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.148-4197T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219889 | |||||||
chr3:142220367 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(145): Show |
157 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.148-4675G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220367 | |||||||
chr3:142220414 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.148-4722G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220414 | |||||||
chr3:142220424 | C | T | 6 | a0001c0001t0005g0030 a0001c0001t0012g0234 a0001c0001t0012g0235 others(3): Show |
6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-4732G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220424 | |||||||
chr3:142220756 | T | G | 1 | a0001c0001t0046g0155 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.147+4553A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220756 | |||||||
chr3:142221085 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.147+4224A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221085 | |||||||
chr3:142221135 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.147+4174T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221135 | |||||||
chr3:142221243 | T | G | 1 | a0001c0001t0043g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.147+4066A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221243 | |||||||
chr3:142221486 | C | T | 28 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0228 others(25): Show |
28 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.147+3823G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221486 | |||||||
chr3:142221977 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147+3332T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221977 | |||||||
chr3:142222033 | T | C | 2 | a0001c0001t0030g0153 a0001c0001t0033g0154 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.147+3276A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222033 | |||||||
chr3:142222210 | G | C | 2 | a0001c0001t0020g0137 a0001c0001t0020g0138 |
2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.147+3099C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222210 | |||||||
chr3:142222266 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
185 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.147+3043T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222266 | |||||||
chr3:142222267 | A | T | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0005g0210 others(1): Show |
4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+3042T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222267 | |||||||
chr3:142222391 | C | G | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0005g0210 others(1): Show |
4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2918G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222391 | |||||||
chr3:142222490 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.147+2819C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222490 | |||||||
chr3:142223018 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.147+2291G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223018 | |||||||
chr3:142223024 | G | C | 1 | a0001c0001t0046g0155 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.147+2285C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223024 | |||||||
chr3:142223358 | T | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(182): Show |
194 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.147+1951A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223358 | |||||||
chr3:142223524 | G | C | 1 | a0001c0001t0004g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.147+1785C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223524 | |||||||
chr3:142223837 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(242): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.147+1472T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223837 | |||||||
chr3:142224176 | G | A | 2 | a0001c0002t0006g0251 a0001c0002t0013g0252 |
2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.147+1133C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224176 | |||||||
chr3:142224695 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.147+614T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224695 | |||||||
chr3:142224747 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.147+562C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224747 | |||||||
chr3:142224766 | A | G | 1 | a0001c0001t0005g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147+543T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224766 | |||||||
chr3:142224771 | A | G | 3 | a0001c0001t0004g0028 a0001c0001t0052g0027 a0001c0001t0066g0026 |
3 | HG02523.hp2 NA18612.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.147+538T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224771 | |||||||
chr3:142224786 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.147+523G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224786 | |||||||
chr3:142224852 | GA | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(8): Show |
11 | HG01192.hp2 HG02071.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+456delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224852 | |||||||
chr3:142224897 | G | A | 1 | a0001c0001t0013g0255 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.147+412C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224897 |