geneid | 4820 |
---|---|
ensemblid | ENSG00000114857.19 |
hgncid | 7833 |
symbol | NKTR |
name | natural killer cell triggering receptor |
refseq_nuc | NM_005385.4 |
refseq_prot | NP_005376.2 |
ensembl_nuc | ENST00000232978.13 |
ensembl_prot | ENSP00000232978.8 |
mane_status | MANE Select |
chr | chr3 |
start | 42600686 |
end | 42648735 |
strand | + |
ver | v1.2 |
region | chr3:42600686-42648735 |
region5000 | chr3:42595686-42653735 |
regionname0 | NKTR_chr3_42600686_42648735 |
regionname5000 | NKTR_chr3_42595686_42653735 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1462 | 257 | 48 | 53 | 116 | 10 | 28 | 89 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002 | 0/0 | 1462 | 37 | 6 | 3 | 25 | 1 | 2 | 21 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003 | 0/0 | 1462 | 33 | 23 | 5 | 1 | 0 | 4 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0004 | 0/0 | 1462 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0005 | 0/0 | 1462 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0006 | 0/0 | 1462 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0007 | 0/0 | 1462 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0008 | 0/0 | 1462 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0009 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0010 | 0/0 | 1462 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0011 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0012 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0013 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0014 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0015 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0016 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4389 | 249 | 47 | 52 | 111 | 9 | 28 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0002 | 0/0 | 4389 | 31 | 22 | 4 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0003 | 0/0 | 4389 | 25 | 1 | 1 | 22 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0004 | 0/0 | 4389 | 12 | 5 | 2 | 3 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0005 | 0/0 | 4389 | 6 | 6 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0006 | 0/0 | 4389 | 5 | 5 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0007 | 0/0 | 4389 | 3 | 1 | 1 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0008 | 0/0 | 4389 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0009 | 0/0 | 4389 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0010 | 0/0 | 4389 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0011 | 0/0 | 4389 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0012 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0013 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0014 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0015 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0016 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0017 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0018 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0019 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0020 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0021 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0022 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
c0023 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2877 | 59 | 5 | 11 | 29 | 5 | 7 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0002 | 0/0 | 2879 | 58 | 4 | 14 | 35 | 0 | 5 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0003 | 0/0 | 2888 | 44 | 4 | 3 | 30 | 1 | 6 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0004 | 0/0 | 2890 | 18 | 1 | 5 | 9 | 2 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0005 | 0/0 | 2881 | 14 | 2 | 8 | 1 | 2 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0006 | 0/0 | 2890 | 11 | 1 | 2 | 6 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0007 | 0/0 | 2888 | 9 | 6 | 1 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0008 | 0/0 | 2883 | 8 | 0 | 3 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0009 | 0/0 | 2884 | 8 | 7 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0010 | 0/0 | 2886 | 8 | 7 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0011 | 0/0 | 2882 | 7 | 5 | 1 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0012 | 0/0 | 2888 | 6 | 1 | 1 | 0 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0013 | 0/0 | 2892 | 6 | 1 | 2 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0014 | 0/0 | 2894 | 6 | 1 | 1 | 4 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0015 | 0/0 | 2888 | 5 | 5 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0016 | 0/0 | 2890 | 5 | 4 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0017 | 0/0 | 2892 | 5 | 1 | 1 | 2 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0018 | 0/0 | 2877 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0019 | 0/0 | 2877 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0020 | 0/0 | 2888 | 4 | 0 | 4 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0021 | 0/0 | 2871 | 3 | 1 | 1 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0022 | 0/0 | 2885 | 3 | 0 | 2 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0023 | 0/0 | 2886 | 3 | 1 | 1 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0024 | 0/0 | 2890 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0025 | 0/0 | 2896 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0026 | 0/0 | 2864 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0027 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0028 | 0/0 | 2884 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0029 | 0/0 | 2887 | 2 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0030 | 0/0 | 2888 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0031 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0032 | 0/0 | 2894 | 2 | 0 | 1 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0033 | 0/0 | 2902 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0034 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0035 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0036 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0037 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0038 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0039 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0040 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0041 | 0/0 | 2877 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0042 | 0/0 | 2882 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0043 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0044 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0045 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0046 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0047 | 0/0 | 2890 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0048 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0049 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0050 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0051 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0052 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0053 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0054 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0055 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0056 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0057 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0058 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0059 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0060 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0061 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0062 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
t0063 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 2 | 3 | 3 | 0 | 3 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0002 | 0/0 | 7 | 1 | 1 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4389 | 249 | 47 | 52 | 111 | 9 | 28 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0007 | 0/0 | 4389 | 3 | 1 | 1 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0008 | 0/0 | 4389 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0012 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0013 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003 | 0/0 | 4389 | 25 | 1 | 1 | 22 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0004 | 0/0 | 4389 | 12 | 5 | 2 | 3 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002 | 0/0 | 4389 | 31 | 22 | 4 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0015 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0019 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0004c0005 | 0/0 | 4389 | 6 | 6 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0005c0006 | 0/0 | 4389 | 5 | 5 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0006c0010 | 0/0 | 4389 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0007c0009 | 0/0 | 4389 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0008c0011 | 0/0 | 4389 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0009c0023 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0010c0021 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0011c0020 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0012c0018 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0013c0017 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0014c0016 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0015c0022 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0016c0014 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7265 | 55 | 5 | 9 | 28 | 4 | 7 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0002 | 0/0 | 7267 | 58 | 4 | 14 | 35 | 0 | 5 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0003 | 0/0 | 7276 | 41 | 4 | 3 | 27 | 1 | 6 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0004 | 0/0 | 7278 | 16 | 1 | 5 | 7 | 2 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0005 | 0/0 | 7269 | 11 | 1 | 7 | 1 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0008 | 0/0 | 7271 | 8 | 0 | 3 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0009 | 0/0 | 7272 | 8 | 7 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0010 | 0/0 | 7274 | 4 | 3 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0011 | 0/0 | 7270 | 7 | 5 | 1 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0013 | 0/0 | 7280 | 5 | 0 | 2 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0018 | 0/0 | 7265 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0020 | 0/0 | 7276 | 4 | 0 | 4 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0021 | 0/0 | 7259 | 3 | 1 | 1 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0022 | 0/0 | 7273 | 3 | 0 | 2 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0027 | 0/0 | 7265 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0029 | 0/0 | 7275 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0030 | 0/0 | 7276 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0032 | 0/0 | 7282 | 2 | 0 | 1 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0034 | 0/0 | 7265 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0036 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0038 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0039 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0040 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0041 | 0/0 | 7265 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0043 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0046 | 0/0 | 7278 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0048 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0052 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0054 | 0/0 | 7286 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0060 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0061 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0001t0063 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0007t0005 | 0/0 | 7269 | 2 | 1 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0007t0029 | 0/0 | 7275 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0008t0024 | 0/0 | 7278 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0012t0001 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0001c0013t0059 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0006 | 0/0 | 7278 | 5 | 0 | 0 | 5 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0014 | 0/0 | 7282 | 4 | 0 | 0 | 4 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0017 | 0/0 | 7280 | 4 | 0 | 1 | 2 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0023 | 0/0 | 7274 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0025 | 0/0 | 7284 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0033 | 0/0 | 7290 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0042 | 0/0 | 7270 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0049 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0050 | 0/0 | 7280 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0051 | 0/0 | 7283 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0053 | 0/0 | 7283 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0055 | 0/0 | 7286 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0003t0062 | 0/0 | 7280 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0004t0006 | 0/0 | 7278 | 3 | 0 | 0 | 1 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0004t0007 | 0/0 | 7276 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0004t0014 | 0/0 | 7282 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0004t0015 | 0/0 | 7276 | 5 | 5 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0002c0004t0047 | 0/0 | 7278 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0006 | 0/0 | 7278 | 3 | 1 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0007 | 0/0 | 7276 | 6 | 5 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0012 | 0/0 | 7276 | 5 | 1 | 0 | 0 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0014 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0016 | 0/0 | 7278 | 4 | 3 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0017 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0023 | 0/0 | 7274 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0028 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0031 | 0/0 | 7280 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0035 | 0/0 | 7274 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0045 | 0/0 | 7274 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0056 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0057 | 0/0 | 7278 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0002t0058 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0015t0028 | 0/0 | 7272 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0003c0019t0016 | 0/0 | 7278 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0004c0005t0010 | 0/0 | 7274 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0004c0005t0037 | 0/0 | 7274 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0004c0005t0044 | 0/0 | 7274 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0005c0006t0013 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0005c0006t0019 | 0/0 | 7265 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0006c0010t0001 | 0/0 | 7265 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0007c0009t0003 | 0/0 | 7276 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0008c0011t0026 | 0/0 | 7252 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0009c0023t0007 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0010c0021t0001 | 0/0 | 7265 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0011c0020t0005 | 0/0 | 7269 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0012c0018t0012 | 0/0 | 7276 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0013c0017t0003 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0014c0016t0004 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0015c0022t0004 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
a0016c0014t0025 | 0/0 | 7284 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | copy fasta | chr3 | 42595686 | 42653735 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0001 | 0/0 | 7 | 1 | 1 | 3 | 0 | 2 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0010g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0011g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0011g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0011g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0013g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0013g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0013g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0018g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0018g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0018g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0020g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0020g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0021g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0021g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0021g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0022g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0022g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0022g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0027g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0027g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0029g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0030g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0030g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0032g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0032g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0034g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0034g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0036g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0038g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0039g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0040g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0041g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0043g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0046g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0048g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0052g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0054g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0060g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0061g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0001t0063g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0007t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0007t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0007t0029g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0008t0024g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0008t0024g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0008t0024g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0012t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0001c0013t0059g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0006g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0014g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0014g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0014g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0017g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0017g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0017g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0023g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0025g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0025g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0033g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0033g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0042g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0049g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0050g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0051g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0053g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0055g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0003t0062g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0014g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0015g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0015g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0015g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0015g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0002c0004t0047g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0007g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0012g0002 | 0/0 | 5 | 1 | 0 | 0 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0014g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0016g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0017g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0023g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0023g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0028g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0031g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0031g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0035g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0045g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0056g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0057g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0002t0058g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0015t0028g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0003c0019t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0004c0005t0010g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0004c0005t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0004c0005t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0004c0005t0037g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0004c0005t0044g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0005c0006t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0005c0006t0019g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0005c0006t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0006c0010t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0007c0009t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0007c0009t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0008c0011t0026g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0008c0011t0026g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0009c0023t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0010c0021t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0011c0020t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0012c0018t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0013c0017t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0014c0016t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0015c0022t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
a0016c0014t0025g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00099 | hp2 | a0001 | c0007 | t0005 | g0176 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0108 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00280 | hp1 | a0002 | c0004 | t0006 | g0060 | EUR | FIN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00280 | hp2 | a0001 | c0001 | t0021 | g0238 | EUR | FIN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00423 | hp2 | a0001 | c0001 | t0048 | g0115 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00544 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00558 | hp1 | a0002 | c0003 | t0051 | g0067 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00597 | hp2 | a0002 | c0003 | t0055 | g0070 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00639 | hp2 | a0002 | c0004 | t0047 | g0058 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00642 | hp1 | a0001 | c0001 | t0008 | g0237 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00673 | hp1 | a0002 | c0003 | t0053 | g0072 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0213 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00741 | hp1 | a0001 | c0001 | t0013 | g0114 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG00741 | hp2 | a0001 | c0001 | t0020 | g0001 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0212 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0225 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0128 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01081 | hp1 | a0011 | c0020 | t0005 | g0156 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01081 | hp2 | a0006 | c0010 | t0001 | g0029 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01106 | hp1 | a0002 | c0004 | t0014 | g0061 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0157 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01109 | hp2 | a0003 | c0015 | t0028 | g0053 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01167 | hp1 | a0003 | c0002 | t0006 | g0045 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01169 | hp1 | a0003 | c0002 | t0006 | g0046 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01169 | hp2 | a0001 | c0001 | t0021 | g0198 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0240 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01192 | hp1 | a0003 | c0002 | t0023 | g0040 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01243 | hp2 | a0008 | c0011 | t0026 | g0287 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01256 | hp1 | a0001 | c0001 | t0020 | g0023 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01256 | hp2 | a0001 | c0007 | t0029 | g0171 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01257 | hp1 | a0001 | c0001 | t0013 | g0106 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0100 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01346 | hp1 | a0012 | c0018 | t0012 | g0002 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01358 | hp2 | a0001 | c0001 | t0020 | g0001 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0174 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0284 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0251 | EUR | IBS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01891 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01891 | hp2 | a0003 | c0002 | t0035 | g0013 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01934 | hp2 | a0003 | c0002 | t0007 | g0012 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01943 | hp1 | a0001 | c0001 | t0022 | g0026 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01943 | hp2 | a0001 | c0001 | t0020 | g0023 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0236 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01975 | hp1 | a0001 | c0001 | t0022 | g0197 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02027 | hp2 | a0002 | c0003 | t0023 | g0073 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02040 | hp1 | a0001 | c0001 | t0032 | g0119 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02040 | hp2 | a0001 | c0013 | t0059 | g0116 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02056 | hp1 | a0014 | c0016 | t0004 | g0022 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02083 | hp2 | a0001 | c0001 | t0060 | g0289 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0089 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | CDX | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CDX | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02257 | hp1 | a0002 | c0003 | t0042 | g0065 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02257 | hp2 | a0001 | c0001 | t0021 | g0255 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02258 | hp1 | a0004 | c0005 | t0037 | g0011 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02293 | hp2 | a0006 | c0010 | t0001 | g0029 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02300 | hp1 | a0002 | c0003 | t0017 | g0004 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0026 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02451 | hp1 | a0003 | c0002 | t0012 | g0002 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02451 | hp2 | a0001 | c0001 | t0027 | g0230 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02572 | hp1 | a0001 | c0001 | t0052 | g0085 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02572 | hp2 | a0004 | c0005 | t0044 | g0142 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0258 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02622 | hp1 | a0005 | c0006 | t0013 | g0082 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02622 | hp2 | a0003 | c0002 | t0016 | g0005 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02630 | hp1 | a0003 | c0002 | t0031 | g0052 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02630 | hp2 | a0001 | c0001 | t0018 | g0149 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02647 | hp1 | a0001 | c0001 | t0046 | g0084 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02647 | hp2 | a0004 | c0005 | t0010 | g0011 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0205 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02723 | hp1 | a0003 | c0002 | t0058 | g0050 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0286 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02809 | hp1 | a0001 | c0001 | t0034 | g0144 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0124 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02818 | hp1 | a0003 | c0002 | t0045 | g0051 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02886 | hp1 | a0004 | c0005 | t0010 | g0129 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02886 | hp2 | a0001 | c0001 | t0018 | g0145 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02895 | hp1 | a0005 | c0006 | t0019 | g0083 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02895 | hp2 | a0003 | c0002 | t0007 | g0039 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0125 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02896 | hp2 | a0003 | c0002 | t0007 | g0036 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02897 | hp1 | a0005 | c0006 | t0019 | g0008 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02897 | hp2 | a0001 | c0001 | t0043 | g0126 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02922 | hp1 | a0003 | c0002 | t0035 | g0013 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02922 | hp2 | a0005 | c0006 | t0019 | g0008 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02965 | hp2 | a0003 | c0002 | t0007 | g0038 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02976 | hp2 | a0005 | c0006 | t0019 | g0008 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03017 | hp2 | a0001 | c0001 | t0008 | g0030 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03041 | hp1 | a0001 | c0001 | t0027 | g0231 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03041 | hp2 | a0004 | c0005 | t0010 | g0011 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03130 | hp2 | a0003 | c0002 | t0028 | g0032 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03139 | hp1 | a0002 | c0004 | t0015 | g0055 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03139 | hp2 | a0003 | c0002 | t0017 | g0035 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03195 | hp1 | a0003 | c0002 | t0057 | g0034 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03209 | hp1 | a0001 | c0001 | t0063 | g0150 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0127 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03225 | hp1 | a0001 | c0001 | t0018 | g0147 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03239 | hp1 | a0003 | c0002 | t0012 | g0002 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03239 | hp2 | a0001 | c0001 | t0022 | g0030 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03453 | hp1 | a0002 | c0004 | t0015 | g0057 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03453 | hp2 | a0003 | c0002 | t0031 | g0005 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03486 | hp1 | a0003 | c0002 | t0016 | g0005 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0135 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03490 | hp1 | a0003 | c0002 | t0012 | g0002 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0266 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03492 | hp1 | a0003 | c0002 | t0012 | g0002 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03516 | hp1 | a0002 | c0004 | t0015 | g0054 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03516 | hp2 | a0003 | c0002 | t0016 | g0048 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03540 | hp2 | a0001 | c0001 | t0030 | g0086 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03579 | hp1 | a0001 | c0001 | t0030 | g0087 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0285 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03654 | hp2 | a0002 | c0003 | t0017 | g0007 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03688 | hp1 | a0003 | c0002 | t0012 | g0002 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03704 | hp1 | a0002 | c0004 | t0006 | g0062 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03710 | hp1 | a0001 | c0001 | t0054 | g0001 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03710 | hp2 | a0001 | c0001 | t0041 | g0166 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0139 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG04199 | hp2 | a0001 | c0001 | t0029 | g0275 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG04204 | hp2 | a0001 | c0001 | t0008 | g0254 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18612 | hp2 | a0001 | c0001 | t0013 | g0091 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18747 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18906 | hp1 | a0002 | c0004 | t0015 | g0056 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18906 | hp2 | a0001 | c0001 | t0034 | g0146 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18941 | hp1 | a0002 | c0004 | t0006 | g0014 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18949 | hp2 | a0001 | c0001 | t0038 | g0164 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18954 | hp1 | a0002 | c0004 | t0007 | g0014 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18960 | hp2 | a0002 | c0003 | t0014 | g0076 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18961 | hp2 | a0007 | c0009 | t0003 | g0003 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18963 | hp2 | a0002 | c0004 | t0007 | g0064 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18964 | hp1 | a0002 | c0003 | t0006 | g0006 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18964 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18965 | hp1 | a0002 | c0003 | t0033 | g0015 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18965 | hp2 | a0007 | c0009 | t0003 | g0095 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18966 | hp2 | a0002 | c0003 | t0025 | g0075 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18967 | hp1 | a0001 | c0001 | t0013 | g0113 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18967 | hp2 | a0001 | c0001 | t0061 | g0276 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18969 | hp1 | a0001 | c0008 | t0024 | g0292 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18971 | hp1 | a0002 | c0003 | t0006 | g0006 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18978 | hp2 | a0002 | c0003 | t0006 | g0069 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18982 | hp2 | a0003 | c0002 | t0016 | g0002 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18983 | hp1 | a0002 | c0003 | t0006 | g0006 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18985 | hp2 | a0002 | c0003 | t0049 | g0074 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18991 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18994 | hp1 | a0002 | c0003 | t0006 | g0015 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18997 | hp1 | a0013 | c0017 | t0003 | g0022 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19011 | hp1 | a0002 | c0003 | t0033 | g0071 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19030 | hp1 | a0003 | c0002 | t0023 | g0041 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19030 | hp2 | a0002 | c0004 | t0015 | g0059 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19043 | hp1 | a0003 | c0002 | t0006 | g0047 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19043 | hp2 | a0001 | c0001 | t0039 | g0218 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19057 | hp2 | a0002 | c0003 | t0014 | g0068 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19059 | hp1 | a0016 | c0014 | t0025 | g0063 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19059 | hp2 | a0001 | c0001 | t0036 | g0290 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19062 | hp1 | a0002 | c0003 | t0050 | g0004 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19065 | hp1 | a0001 | c0001 | t0009 | g0092 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19072 | hp1 | a0002 | c0003 | t0017 | g0077 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19074 | hp1 | a0001 | c0001 | t0013 | g0120 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19075 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19076 | hp1 | a0001 | c0008 | t0024 | g0294 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19077 | hp2 | a0002 | c0003 | t0014 | g0066 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19079 | hp1 | a0002 | c0003 | t0062 | g0004 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19080 | hp1 | a0001 | c0008 | t0024 | g0293 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19080 | hp2 | a0002 | c0003 | t0014 | g0007 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19089 | hp2 | a0002 | c0003 | t0025 | g0004 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19090 | hp1 | a0002 | c0003 | t0017 | g0007 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19090 | hp2 | a0015 | c0022 | t0004 | g0101 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19240 | hp1 | a0003 | c0019 | t0016 | g0049 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA19240 | hp2 | a0004 | c0005 | t0010 | g0131 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20129 | hp1 | a0003 | c0002 | t0007 | g0012 | AFR | ASW | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20129 | hp2 | a0003 | c0002 | t0007 | g0037 | AFR | ASW | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20752 | hp1 | a0010 | c0021 | t0001 | g0192 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0099 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | GIH | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | GIH | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01123 | hp1 | a0001 | c0001 | t0032 | g0003 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02109 | hp1 | a0001 | c0007 | t0005 | g0159 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02109 | hp2 | a0001 | c0001 | t0018 | g0148 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03471 | hp1 | a0008 | c0011 | t0026 | g0288 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG03471 | hp2 | a0009 | c0023 | t0007 | g0044 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0134 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA18955 | hp2 | a0001 | c0012 | t0001 | g0200 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20300 | hp1 | a0003 | c0002 | t0056 | g0043 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA20300 | hp2 | a0001 | c0001 | t0040 | g0009 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
NA21309 | hp2 | a0003 | c0002 | t0014 | g0042 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0220 | REF | REF | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0207 | REF | REF | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42619708
|
G | A | 1 | a0016 | 1 | NA19059.hp1 | missense_variant&splice_region_variant | MODERATE | c.286G>A | p.Asp96Asn | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/17 | 402/7265 | 286/4389 | 96/1462 | chr3 | 42619708 | ||
chr3:42633618
|
T | G | 1 | a0004 | 6 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
missense_variant | MODERATE | c.812T>G | p.Val271Gly | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/17 | 928/7265 | 812/4389 | 271/1462 | chr3 | 42633618 | ||
chr3:42633713
|
G | T | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.907G>T | p.Val303Phe | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/17 | 1023/7265 | 907/4389 | 303/1462 | chr3 | 42633713 | ||
chr3:42634648
|
A | G | 1 | a0015 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.965A>G | p.Gln322Arg | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/17 | 1081/7265 | 965/4389 | 322/1462 | chr3 | 42634648 | ||
chr3:42637454
|
C | T | 1 | a0005 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.1750C>T | p.Pro584Ser | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 1866/7265 | 1750/4389 | 584/1462 | chr3 | 42637454 | ||
chr3:42637658
|
T | G | 1 | a0014 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1954T>G | p.Leu652Val | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2070/7265 | 1954/4389 | 652/1462 | chr3 | 42637658 | ||
chr3:42637686
|
C | T | 1 | a0010 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1982C>T | p.Ser661Leu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2098/7265 | 1982/4389 | 661/1462 | chr3 | 42637686 | ||
chr3:42637994
|
A | G | 1 | a0011 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2290A>G | p.Lys764Glu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2406/7265 | 2290/4389 | 764/1462 | chr3 | 42637994 | ||
chr3:42638006
|
G | A | 1 | a0012 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2302G>A | p.Val768Ile | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2418/7265 | 2302/4389 | 768/1462 | chr3 | 42638006 | ||
chr3:42638184
|
A | C | 1 | a0013 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.2480A>C | p.Lys827Thr | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2596/7265 | 2480/4389 | 827/1462 | chr3 | 42638184 | ||
chr3:42638185
|
G | C | 1 | a0013 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.2481G>C | p.Lys827Asn | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2597/7265 | 2481/4389 | 827/1462 | chr3 | 42638185 | ||
chr3:42638285
|
T | G | 6 | a0002a0003a0008others(3): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
missense_variant | MODERATE | c.2581T>G | p.Leu861Val | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2697/7265 | 2581/4389 | 861/1462 | chr3 | 42638285 | ||
chr3:42638508
|
C | T | 3 | a0002a0006a0016 | 40 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
missense_variant | MODERATE | c.2804C>T | p.Ser935Leu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2920/7265 | 2804/4389 | 935/1462 | chr3 | 42638508 | ||
chr3:42638541
|
G | C | 1 | a0008 | 2 | HG01243.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.2837G>C | p.Gly946Ala | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2953/7265 | 2837/4389 | 946/1462 | chr3 | 42638541 | ||
chr3:42638979
|
C | G | 1 | a0007 | 2 | NA18961.hp2 NA18965.hp2 |
missense_variant | MODERATE | c.3275C>G | p.Ser1092Cys | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 3391/7265 | 3275/4389 | 1092/1462 | chr3 | 42638979 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42617589
|
G | A | 1 | a0001c0012 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.78G>A | p.Gln26Gln | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/17 | 194/7265 | 78/4389 | 26/1462 | chr3 | 42617589 | ||
chr3:42617637
|
G | A | 1 | a0001c0013 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.126G>A | p.Leu42Leu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/17 | 242/7265 | 126/4389 | 42/1462 | chr3 | 42617637 | ||
chr3:42619075
|
G | A | 1 | a0001c0007 | 3 | HG00099.hp2 HG01256.hp2 HG02109.hp1 |
synonymous_variant | LOW | c.189G>A | p.Thr63Thr | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/17 | 305/7265 | 189/4389 | 63/1462 | chr3 | 42619075 | ||
chr3:42632602
|
T | C | 1 | a0003c0015 | 1 | HG01109.hp2 | splice_region_variant&synonymous_variant | LOW | c.552T>C | p.Val184Val | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/17 | 668/7265 | 552/4389 | 184/1462 | chr3 | 42632602 | ||
chr3:42637918
|
T | C | 1 | a0013c0017 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.2214T>C | p.Cys738Cys | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2330/7265 | 2214/4389 | 738/1462 | chr3 | 42637918 | ||
chr3:42638005
|
C | T | 10 | a0001c0008a0002c0003a0002c0004others(7): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
synonymous_variant | LOW | c.2301C>T | p.Ser767Ser | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2417/7265 | 2301/4389 | 767/1462 | chr3 | 42638005 | ||
chr3:42638053
|
T | C | 1 | a0003c0019 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.2349T>C | p.Ser783Ser | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2465/7265 | 2349/4389 | 783/1462 | chr3 | 42638053 | ||
chr3:42638201
|
A | C | 1 | a0013c0017 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.2497A>C | p.Arg833Arg | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2613/7265 | 2497/4389 | 833/1462 | chr3 | 42638201 | ||
chr3:42638356
|
A | G | 2 | a0002c0003a0016c0014 | 26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
synonymous_variant | LOW | c.2652A>G | p.Lys884Lys | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2768/7265 | 2652/4389 | 884/1462 | chr3 | 42638356 | ||
chr3:42639034
|
C | T | 1 | a0001c0008 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
synonymous_variant | LOW | c.3330C>T | p.His1110His | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 3446/7265 | 3330/4389 | 1110/1462 | chr3 | 42639034 | ||
chr3:42639610
|
G | A | 1 | a0001c0008 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
synonymous_variant | LOW | c.3906G>A | p.Thr1302Thr | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 4022/7265 | 3906/4389 | 1302/1462 | chr3 | 42639610 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42600774
|
G | C | 1 | a0001c0001t0036 | 1 | NA19059.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/17 | 233 | chr3 | 42600774 | |||||
chr3:42600775
|
C | G | 2 | a0001c0001t0036a0001c0001t0063 | 2 | HG03209.hp1 NA19059.hp2 |
5_prime_UTR_variant | MODIFIER | c.-27C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/17 | 232 | chr3 | 42600775 | |||||
chr3:42646131
|
G | T | 1 | a0002c0003t0062 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 156 | chr3 | 42646131 | |||||
chr3:42646229
|
C | T | 1 | a0001c0001t0020 | 4 | HG00741.hp2 HG01256.hp1 HG01358.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*254C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 254 | chr3 | 42646229 | |||||
chr3:42646368
|
G | C | 1 | a0004c0005t0037 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 393 | chr3 | 42646368 | |||||
chr3:42646415
|
T | C | 1 | a0001c0001t0038 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 440 | chr3 | 42646415 | |||||
chr3:42646449
|
A | C | 1 | a0001c0001t0061 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 474 | chr3 | 42646449 | |||||
chr3:42646745
|
C | T | 2 | a0001c0001t0060a0001c0013t0059 | 2 | HG02040.hp2 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*770C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 770 | chr3 | 42646745 | |||||
chr3:42646830
|
T | G | 1 | a0008c0011t0026 | 2 | HG01243.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*855T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 855 | chr3 | 42646830 | |||||
chr3:42647086
|
C | G | 4 | a0003c0002t0035a0003c0002t0056a0003c0002t0057others(1): Show | 5 | HG01891.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1111 | chr3 | 42647086 | |||||
chr3:42647241
|
C | G | 1 | a0008c0011t0026 | 2 | HG01243.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1266C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1266 | chr3 | 42647241 | |||||
chr3:42647267
|
A | AGT | 1 | a0001c0001t0002 | 58 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1326_*1327dupTG | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | ||||
chr3:42647267
|
A | AGTGT | 3 | a0001c0001t0005a0001c0007t0005a0011c0020t0005 | 14 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1324_*1327dupTGTG | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | ||||
chr3:42647267
|
A | AGTGTGT | 2 | a0001c0001t0008a0001c0001t0043 | 9 | HG00642.hp1 HG01361.hp2 HG02300.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1322_*1327dupTGTG others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | ||||
chr3:42647267
|
A | AGTGTGTG others(1): Show |
1 | a0001c0001t0022 | 3 | HG01943.hp1 HG01975.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1320_*1327dupTGTG others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | ||||
chr3:42647267
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0029a0001c0007t0029 | 2 | HG01256.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1318_*1327dupTGTG others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | ||||
chr3:42647267
|
AGTGTGT | A | 1 | a0001c0001t0021 | 3 | HG00280.hp2 HG01169.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1322_*1327delTGTG others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1322 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | ||||
chr3:42647288
|
GTGTGTGT others(6): Show |
G | 1 | a0008c0011t0026 | 2 | HG01243.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1314_*1326delTGTG others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1314 | chr3 | 42647288 | |||||
chr3:42647301
|
T | TGTGTG | 2 | a0001c0001t0011a0002c0003t0042 | 8 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(1): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG | 3 | a0001c0001t0009a0003c0002t0028a0003c0015t0028 | 10 | HG01109.hp2 HG02559.hp1 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(2): Show |
8 | a0001c0001t0010a0002c0003t0023a0003c0002t0023others(5): Show | 16 | HG00544.hp1 HG01192.hp1 HG01891.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(4): Show |
13 | a0001c0001t0003a0001c0001t0020a0001c0001t0030others(10): Show | 72 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(7): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(6): Show |
14 | a0001c0001t0004a0001c0001t0036a0001c0001t0046others(11): Show | 42 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(8): Show |
7 | a0001c0001t0013a0002c0003t0017a0002c0003t0050others(4): Show | 15 | HG00741.hp1 HG01257.hp1 HG02300.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(10): Show |
5 | a0001c0001t0032a0001c0001t0052a0002c0003t0014others(2): Show | 9 | HG01106.hp1 HG01123.hp1 HG02040.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(11): Show |
1 | a0002c0003t0051 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(12): Show |
2 | a0002c0003t0025a0016c0014t0025 | 3 | NA18966.hp2 NA19059.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(14): Show |
2 | a0001c0001t0054a0002c0003t0055 | 2 | HG00597.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647301
|
T | TGTGTGTG others(18): Show |
1 | a0002c0003t0033 | 2 | NA18965.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(21): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | ||||
chr3:42647302
|
G | GTGTGTGT others(7): Show |
2 | a0001c0001t0048a0002c0003t0049 | 2 | HG00423.hp2 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | chr3 | 42647302 | |||||
chr3:42647302
|
G | GTGTGTGT others(11): Show |
1 | a0002c0003t0053 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | chr3 | 42647302 | |||||
chr3:42647303
|
G | T | 65 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(62): Show | 192 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | chr3 | 42647303 | |||||
chr3:42647304
|
T | G | 1 | a0001c0001t0039 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1329T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1329 | chr3 | 42647304 | |||||
chr3:42647496
|
C | T | 1 | a0001c0001t0041 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1521C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1521 | chr3 | 42647496 | |||||
chr3:42647617
|
G | T | 37 | a0002c0003t0006a0002c0003t0014a0002c0003t0017others(34): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1642G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1642 | chr3 | 42647617 | |||||
chr3:42647733
|
T | C | 3 | a0001c0001t0030a0001c0001t0046a0001c0001t0052 | 4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1758T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1758 | chr3 | 42647733 | |||||
chr3:42647736
|
A | C | 1 | a0001c0001t0018 | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1761A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1761 | chr3 | 42647736 | |||||
chr3:42647770
|
T | C | 1 | a0001c0008t0024 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1795T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1795 | chr3 | 42647770 | |||||
chr3:42647789
|
C | T | 1 | a0001c0001t0034 | 2 | HG02809.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1814C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1814 | chr3 | 42647789 | |||||
chr3:42648017
|
T | C | 6 | a0003c0002t0012a0003c0002t0016a0003c0002t0031others(3): Show | 14 | HG01346.hp1 HG02451.hp1 HG02622.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2042T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2042 | chr3 | 42648017 | |||||
chr3:42648022
|
T | A | 1 | a0001c0001t0034 | 2 | HG02809.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2047T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2047 | chr3 | 42648022 | |||||
chr3:42648084
|
T | C | 1 | a0001c0001t0018 | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2109T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2109 | chr3 | 42648084 | |||||
chr3:42648212
|
G | A | 2 | a0004c0005t0037a0004c0005t0044 | 2 | HG02258.hp1 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2237G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2237 | chr3 | 42648212 | |||||
chr3:42648236
|
T | C | 1 | a0001c0001t0027 | 2 | HG02451.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2261T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2261 | chr3 | 42648236 | |||||
chr3:42648285
|
T | G | 68 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(65): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2310T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2310 | chr3 | 42648285 | |||||
chr3:42648289
|
A | G | 1 | a0001c0001t0054 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2314A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2314 | chr3 | 42648289 | |||||
chr3:42648302
|
A | G | 1 | a0002c0003t0050 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2327A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2327 | chr3 | 42648302 | |||||
chr3:42648460
|
C | G | 2 | a0002c0004t0015a0002c0004t0047 | 6 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2485C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2485 | chr3 | 42648460 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42600853
|
G | A | 1 | a0003c0002t0028g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24+75G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/16 | chr3 | 42600853 | ||||||
chr3:42600873
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-24+95G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/16 | chr3 | 42600873 | ||||||
chr3:42601121
|
G | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+57G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601121 | ||||||
chr3:42601142
|
T | TC | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+83dupC | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42601142 | |||||
chr3:42601228
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.58+164C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601228 | ||||||
chr3:42601253
|
C | G | 1 | a0001c0001t0036g0290 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.58+189C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601253 | ||||||
chr3:42601254
|
G | C | 1 | a0001c0001t0036g0290 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.58+190G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601254 | ||||||
chr3:42601322
|
C | T | 1 | a0001c0001t0060g0289 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.58+258C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601322 | ||||||
chr3:42601465
|
C | A | 1 | a0001c0001t0036g0290 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.58+401C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601465 | ||||||
chr3:42601485
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.58+421T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601485 | ||||||
chr3:42601579
|
A | G | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+515A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601579 | ||||||
chr3:42601763
|
C | T | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+699C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601763 | ||||||
chr3:42601892
|
G | A | 1 | a0001c0001t0004g0079 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.58+828G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601892 | ||||||
chr3:42601922
|
G | A | 1 | a0003c0002t0057g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58+858G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601922 | ||||||
chr3:42601933
|
G | A | 164 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(161): Show | 191 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.58+869G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601933 | ||||||
chr3:42602108
|
G | A | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.58+1044G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602108 | ||||||
chr3:42602204
|
G | A | 28 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(25): Show | 35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.58+1140G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602204 | ||||||
chr3:42602239
|
G | A | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1175G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602239 | ||||||
chr3:42602246
|
G | C | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.58+1182G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602246 | ||||||
chr3:42602321
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.58+1257G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602321 | ||||||
chr3:42602338
|
G | T | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.58+1274G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602338 | ||||||
chr3:42602353
|
C | A | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1289C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602353 | ||||||
chr3:42602443
|
G | A | 3 | a0003c0002t0012g0002a0003c0002t0016g0002a0012c0018t0012g0002 | 7 | HG01346.hp1 HG02451.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1379G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602443 | ||||||
chr3:42602524
|
CAG | C | 99 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(96): Show | 116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.58+1461_58+1462del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602524 | ||||||
chr3:42602609
|
G | A | 3 | a0001c0001t0003g0016a0001c0001t0004g0016a0001c0001t0004g0080 | 3 | HG01496.hp1 HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.58+1545G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602609 | ||||||
chr3:42602628
|
CTTT | C | 105 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(102): Show | 122 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.58+1580_58+1582del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42602628 | |||||
chr3:42602628
|
CTTTT | C | 62 | a0001c0001t0003g0081a0002c0003t0006g0006a0002c0003t0006g0015others(59): Show | 72 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.58+1579_58+1582del others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42602628 | |||||
chr3:42602659
|
C | T | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1595C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602659 | ||||||
chr3:42602755
|
C | T | 1 | a0002c0003t0025g0075 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.58+1691C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602755 | ||||||
chr3:42602786
|
C | T | 1 | a0004c0005t0044g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.58+1722C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602786 | ||||||
chr3:42602841
|
AC | A | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+1781delC | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42602841 | |||||
chr3:42602885
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.58+1821C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602885 | ||||||
chr3:42602903
|
G | A | 8 | a0003c0002t0007g0012a0003c0002t0007g0036a0003c0002t0007g0037others(5): Show | 9 | HG01192.hp1 HG01934.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+1839G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602903 | ||||||
chr3:42602912
|
G | A | 1 | a0003c0002t0014g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58+1848G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602912 | ||||||
chr3:42602932
|
T | C | 3 | a0005c0006t0013g0082a0005c0006t0019g0008a0005c0006t0019g0083 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1868T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602932 | ||||||
chr3:42603025
|
C | CA | 96 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(93): Show | 112 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.58+1976dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603025 | |||||
chr3:42603195
|
G | GTC | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+2133_58+2134dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603195 | |||||
chr3:42603224
|
G | A | 1 | a0003c0002t0028g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58+2160G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603224 | ||||||
chr3:42603289
|
G | T | 92 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(89): Show | 107 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.58+2225G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603289 | ||||||
chr3:42603340
|
A | G | 3 | a0005c0006t0013g0082a0005c0006t0019g0008a0005c0006t0019g0083 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2276A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603340 | ||||||
chr3:42603360
|
T | TA | 33 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0184others(30): Show | 36 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.58+2321dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | |||||
chr3:42603360
|
T | TAA | 7 | a0001c0001t0002g0158a0001c0001t0002g0160a0001c0001t0002g0161others(4): Show | 7 | HG00639.hp1 HG02109.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+2320_58+2321dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | |||||
chr3:42603360
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0008t0024g0293a0001c0008t0024g0294a0002c0004t0015g0055others(4): Show | 7 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+2314_58+2321del others(8): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | |||||
chr3:42603360
|
TAAAAAAA others(2): Show |
T | 33 | a0002c0004t0006g0014a0002c0004t0006g0060a0002c0004t0006g0062others(30): Show | 40 | HG00280.hp1 HG01106.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.58+2313_58+2321del others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | |||||
chr3:42603360
|
TAAAAAAA others(3): Show |
T | 24 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(21): Show | 27 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.58+2312_58+2321del others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | |||||
chr3:42603360
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0282 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.58+2307_58+2321del others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | |||||
chr3:42603373
|
A | AC | 3 | a0001c0001t0009g0285a0001c0001t0009g0286a0001c0001t0010g0089 | 3 | HG02145.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+2309_58+2310ins others(1): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603373 | ||||||
chr3:42603374
|
A | C | 86 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(83): Show | 101 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.58+2310A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603374 | ||||||
chr3:42603457
|
A | G | 4 | a0001c0001t0001g0031a0001c0001t0001g0184a0001c0001t0001g0281others(1): Show | 5 | HG00423.hp1 NA18944.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2393A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603457 | ||||||
chr3:42603651
|
G | A | 171 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(168): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.58+2587G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603651 | ||||||
chr3:42603732
|
C | CT | 22 | a0001c0001t0001g0078a0001c0001t0001g0272a0001c0001t0001g0274others(19): Show | 23 | HG00673.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.58+2689dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603732 | |||||
chr3:42603732
|
CT | C | 120 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(117): Show | 142 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.58+2689delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603732 | |||||
chr3:42603804
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.58+2740C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603804 | ||||||
chr3:42603881
|
A | G | 1 | a0002c0003t0049g0074 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.58+2817A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603881 | ||||||
chr3:42603976
|
A | T | 4 | a0001c0001t0018g0145a0001c0001t0018g0147a0001c0001t0018g0148others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+2912A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603976 | ||||||
chr3:42603980
|
G | A | 28 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(25): Show | 35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.58+2916G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603980 | ||||||
chr3:42603988
|
C | T | 28 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(25): Show | 35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.58+2924C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603988 | ||||||
chr3:42604205
|
C | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+3141C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604205 | ||||||
chr3:42604379
|
CT | C | 68 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(65): Show | 80 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.58+3325delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604379 | |||||
chr3:42604386
|
T | C | 4 | a0001c0001t0030g0086a0001c0001t0030g0087a0001c0001t0046g0084others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3322T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604386 | ||||||
chr3:42604446
|
A | G | 1 | a0001c0001t0034g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.58+3382A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604446 | ||||||
chr3:42604541
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG01243.hp1 HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58+3477G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604541 | ||||||
chr3:42604659
|
C | CT | 30 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0078others(27): Show | 31 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.58+3634dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTT | 20 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0180others(17): Show | 20 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.58+3633_58+3634dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTT | 12 | a0001c0001t0001g0256a0001c0001t0001g0277a0001c0001t0001g0281others(9): Show | 12 | HG00423.hp1 HG01981.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+3632_58+3634dup others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTT | 6 | a0001c0001t0001g0260a0001c0001t0001g0291a0001c0001t0002g0181others(3): Show | 6 | HG03486.hp2 HG03540.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3631_58+3634dup others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0262others(3): Show | 6 | HG03225.hp2 HG06807.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+3628_58+3634dup others(7): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0264 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.58+3625_58+3634dup others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0265 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.58+3624_58+3634dup others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.58+3623_58+3634dup others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0005g0266 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.58+3622_58+3634dup others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(7): Show |
1 | a0008c0011t0026g0287 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58+3621_58+3634dup others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0267a0001c0001t0030g0087 | 2 | HG03579.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.58+3620_58+3634dup others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0279 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.58+3616_58+3634dup others(19): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(13): Show |
1 | a0008c0011t0026g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.58+3615_58+3634dup others(20): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.58+3613_58+3634dup others(22): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CT | C | 9 | a0001c0001t0001g0143a0001c0001t0001g0191a0001c0001t0001g0193others(6): Show | 9 | HG01099.hp2 HG01192.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3634delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTT | C | 7 | a0001c0001t0001g0190a0001c0001t0003g0130a0001c0001t0009g0010others(4): Show | 8 | HG01074.hp2 HG01167.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3633_58+3634del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0009g0127a0001c0001t0034g0144a0001c0001t0043g0126others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3626_58+3634del others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(3): Show |
C | 24 | a0001c0001t0009g0125a0002c0003t0006g0069a0002c0003t0014g0068others(21): Show | 30 | HG00597.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.58+3625_58+3634del others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(4): Show |
C | 27 | a0001c0001t0002g0158a0001c0001t0002g0165a0002c0003t0006g0006others(24): Show | 31 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.58+3624_58+3634del others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0189a0002c0004t0006g0014a0002c0004t0007g0014others(12): Show | 17 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+3623_58+3634del others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(6): Show |
C | 1 | a0005c0006t0013g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58+3622_58+3634del others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(7): Show |
C | 8 | a0001c0001t0001g0188a0001c0001t0010g0089a0001c0001t0018g0145others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3621_58+3634del others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0004g0123a0001c0001t0011g0009a0001c0001t0040g0009 | 4 | HG01891.hp1 HG02976.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3619_58+3634del others(16): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0001g0187a0001c0001t0002g0271a0001c0001t0003g0021others(4): Show | 8 | HG01981.hp1 HG02015.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+3618_58+3634del others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(11): Show |
C | 62 | a0001c0001t0002g0186a0001c0001t0003g0001a0001c0001t0003g0003others(59): Show | 73 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.58+3617_58+3634del others(18): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604659
|
CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0003g0090a0001c0001t0005g0185a0001c0001t0013g0091 | 3 | HG02965.hp1 NA18612.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.58+3616_58+3634del others(19): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | |||||
chr3:42604941
|
C | T | 1 | a0001c0001t0018g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.58+3877C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604941 | ||||||
chr3:42604985
|
C | T | 1 | a0001c0001t0009g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58+3921C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604985 | ||||||
chr3:42605075
|
T | G | 3 | a0001c0001t0009g0010a0001c0001t0011g0010a0001c0001t0011g0128 | 4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+4011T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605075 | ||||||
chr3:42605115
|
T | C | 2 | a0002c0003t0017g0077a0002c0003t0042g0065 | 2 | HG02257.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.58+4051T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605115 | ||||||
chr3:42605229
|
C | G | 1 | a0001c0001t0013g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.58+4165C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605229 | ||||||
chr3:42605355
|
G | C | 1 | a0003c0002t0017g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.58+4291G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605355 | ||||||
chr3:42605419
|
A | G | 1 | a0002c0004t0006g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+4355A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605419 | ||||||
chr3:42605576
|
C | G | 1 | a0001c0001t0032g0119 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.58+4512C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605576 | ||||||
chr3:42605623
|
T | C | 3 | a0001c0001t0009g0285a0001c0001t0009g0286a0001c0001t0010g0089 | 3 | HG02145.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+4559T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605623 | ||||||
chr3:42605660
|
G | T | 1 | a0009c0023t0007g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.58+4596G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605660 | ||||||
chr3:42605706
|
C | T | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+4642C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605706 | ||||||
chr3:42605707
|
C | T | 1 | a0001c0008t0024g0292 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.58+4643C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605707 | ||||||
chr3:42605853
|
A | G | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+4789A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605853 | ||||||
chr3:42605895
|
A | G | 2 | a0001c0001t0034g0144a0001c0001t0034g0146 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58+4831A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605895 | ||||||
chr3:42606160
|
G | T | 5 | a0001c0001t0003g0132a0001c0001t0009g0125a0001c0001t0009g0127others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+5096G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606160 | ||||||
chr3:42606179
|
A | G | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+5115A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606179 | ||||||
chr3:42606188
|
A | G | 1 | a0002c0004t0015g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58+5124A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606188 | ||||||
chr3:42606247
|
T | TC | 7 | a0001c0001t0001g0234a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 11 | HG01346.hp1 HG02451.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+5190dupC | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42606247 | |||||
chr3:42606277
|
T | C | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+5213T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606277 | ||||||
chr3:42606286
|
T | A | 24 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0021others(21): Show | 26 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.58+5222T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606286 | ||||||
chr3:42606508
|
A | G | 4 | a0001c0001t0018g0145a0001c0001t0018g0147a0001c0001t0018g0148others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5444A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606508 | ||||||
chr3:42606527
|
G | A | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+5463G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606527 | ||||||
chr3:42606867
|
G | A | 1 | a0001c0001t0005g0273 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.58+5803G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606867 | ||||||
chr3:42606868
|
CT | C | 6 | a0001c0001t0003g0130a0004c0005t0010g0011a0004c0005t0010g0129others(3): Show | 7 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+5813delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42606868 | |||||
chr3:42606886
|
A | G | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+5822A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606886 | ||||||
chr3:42607051
|
ATTAG | A | 94 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(91): Show | 109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.58+5992_58+5995del others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607051 | |||||
chr3:42607109
|
C | A | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+6045C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607109 | ||||||
chr3:42607239
|
G | A | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+6175G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607239 | ||||||
chr3:42607270
|
A | G | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.58+6206A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607270 | ||||||
chr3:42607546
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58+6482G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607546 | ||||||
chr3:42607658
|
T | C | 3 | a0005c0006t0013g0082a0005c0006t0019g0008a0005c0006t0019g0083 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+6594T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607658 | ||||||
chr3:42607819
|
A | T | 1 | a0001c0001t0001g0196 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.58+6755A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607819 | ||||||
chr3:42607908
|
G | A | 1 | a0002c0004t0006g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+6844G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607908 | ||||||
chr3:42607967
|
CTCTTTTT others(19): Show |
C | 2 | a0001c0001t0034g0144a0001c0001t0034g0146 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58+6905_58+6930del others(26): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607967 | |||||
chr3:42607969
|
C | CT | 12 | a0001c0001t0001g0196a0001c0001t0001g0219a0001c0001t0001g0252others(9): Show | 12 | HG01069.hp1 HG02109.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+6948dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
C | CTTTTT | 9 | a0001c0001t0001g0178a0001c0001t0001g0220a0001c0001t0001g0221others(6): Show | 9 | HG01109.hp1 HG01981.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+6944_58+6948dup others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
C | CTTTTTT | 13 | a0001c0001t0001g0078a0001c0001t0001g0143a0001c0001t0001g0194others(10): Show | 13 | HG00423.hp1 HG00673.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6943_58+6948dup others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
C | CTTTTTTT | 8 | a0001c0001t0001g0229a0001c0001t0001g0291a0001c0001t0002g0158others(5): Show | 8 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+6942_58+6948dup others(7): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0027g0230a0001c0001t0027g0231 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.58+6939_58+6948dup others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.58+6937_58+6948dup others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0232 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.58+6936_58+6948dup others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.58+6929_58+6948dup others(20): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CT | C | 25 | a0001c0001t0001g0180a0001c0001t0001g0190a0001c0001t0001g0201others(22): Show | 26 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.58+6948delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTT | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0153a0001c0001t0001g0184others(7): Show | 10 | HG00099.hp1 HG01361.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+6947_58+6948del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTT | C | 8 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(5): Show | 8 | HG00280.hp2 HG01243.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+6946_58+6948del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0008g0174a0001c0001t0008g0237a0001c0001t0021g0198 | 3 | HG00642.hp1 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.58+6939_58+6948del others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0008g0030a0001c0001t0022g0030 | 2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.58+6938_58+6948del others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0271 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.58+6937_58+6948del others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0009g0285a0001c0001t0009g0286a0001c0001t0018g0149others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+6936_58+6948del others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0018g0145a0001c0001t0018g0148a0008c0011t0026g0287others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+6935_58+6948del others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(8): Show |
C | 14 | a0001c0001t0002g0183a0001c0001t0002g0244a0001c0001t0002g0265others(11): Show | 17 | HG00558.hp1 HG00597.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+6934_58+6948del others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(9): Show |
C | 55 | a0001c0001t0005g0236a0001c0001t0008g0026a0001c0001t0022g0026others(52): Show | 64 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.58+6933_58+6948del others(16): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(10): Show |
C | 6 | a0001c0001t0002g0235a0001c0001t0005g0266a0001c0001t0022g0197others(3): Show | 6 | HG01167.hp1 HG01433.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+6932_58+6948del others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0002g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.58+6931_58+6948del others(18): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(12): Show |
C | 4 | a0001c0001t0002g0186a0001c0008t0024g0292a0001c0008t0024g0293others(1): Show | 4 | NA18969.hp1 NA19076.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+6930_58+6948del others(19): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0002g0168 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.58+6929_58+6948del others(20): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0001g0188 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.58+6927_58+6948del others(22): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0046g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.58+6926_58+6948del others(23): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(22): Show |
C | 2 | a0001c0001t0030g0086a0001c0001t0030g0087 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58+6920_58+6948del others(29): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(23): Show |
C | 12 | a0001c0001t0003g0003a0001c0001t0003g0094a0001c0001t0003g0096others(9): Show | 13 | HG00544.hp1 HG01123.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+6919_58+6948del others(30): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42607969
|
CTTTTTTT others(24): Show |
C | 75 | a0001c0001t0003g0001a0001c0001t0003g0016a0001c0001t0003g0017others(72): Show | 89 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.58+6918_58+6948del others(31): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | |||||
chr3:42608075
|
C | T | 4 | a0003c0002t0035g0013a0003c0002t0056g0043a0003c0002t0057g0034others(1): Show | 5 | HG01891.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+7011C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608075 | ||||||
chr3:42608076
|
G | A | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.58+7012G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608076 | ||||||
chr3:42608082
|
C | T | 1 | a0003c0002t0007g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.58+7018C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608082 | ||||||
chr3:42608107
|
A | G | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+7043A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608107 | ||||||
chr3:42608112
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.58+7048C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608112 | ||||||
chr3:42608249
|
C | T | 1 | a0001c0012t0001g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.58+7185C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608249 | ||||||
chr3:42608319
|
A | G | 1 | a0001c0001t0005g0251 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.58+7255A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608319 | ||||||
chr3:42608439
|
G | A | 4 | a0001c0001t0030g0086a0001c0001t0030g0087a0001c0001t0046g0084others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+7375G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608439 | ||||||
chr3:42608463
|
G | A | 4 | a0001c0001t0005g0240a0001c0001t0008g0174a0001c0001t0008g0237others(1): Show | 4 | HG00642.hp1 HG01169.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+7399G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608463 | ||||||
chr3:42608557
|
T | A | 1 | a0001c0001t0001g0281 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.58+7493T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608557 | ||||||
chr3:42608610
|
G | A | 1 | a0003c0002t0045g0051 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+7546G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608610 | ||||||
chr3:42608901
|
A | G | 165 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(162): Show | 192 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.58+7837A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608901 | ||||||
chr3:42609058
|
G | A | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+7994G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609058 | ||||||
chr3:42609128
|
C | CA | 14 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.58+8077dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609128 | |||||
chr3:42609139
|
A | AAAG | 42 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(39): Show | 48 | HG00280.hp1 HG00639.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.58+8081_58+8083dup others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609139 | |||||
chr3:42609139
|
A | AGAAG | 23 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(20): Show | 26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58+8075_58+8076ins others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609139 | ||||||
chr3:42609155
|
A | C | 1 | a0001c0001t0002g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.58+8091A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609155 | ||||||
chr3:42609208
|
A | G | 2 | a0001c0001t0004g0099a0001c0001t0004g0100 | 2 | HG01257.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.58+8144A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609208 | ||||||
chr3:42609234
|
CAG | C | 19 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(16): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+8173_58+8174del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609234 | |||||
chr3:42609365
|
A | G | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.59-8205A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609365 | ||||||
chr3:42609501
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.59-8069T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609501 | ||||||
chr3:42609522
|
G | C | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-8048G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609522 | ||||||
chr3:42609629
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.59-7941A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609629 | ||||||
chr3:42609646
|
G | T | 1 | a0001c0001t0003g0098 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.59-7924G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609646 | ||||||
chr3:42609717
|
C | T | 18 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(15): Show | 24 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-7853C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609717 | ||||||
chr3:42609802
|
G | A | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.59-7768G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609802 | ||||||
chr3:42609827
|
G | T | 171 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(168): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-7743G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609827 | ||||||
chr3:42609850
|
T | TAA | 19 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(16): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-7719_59-7718dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609850 | |||||
chr3:42609973
|
C | A | 171 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(168): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-7597C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609973 | ||||||
chr3:42610011
|
C | CT | 4 | a0001c0001t0003g0130a0005c0006t0013g0082a0005c0006t0019g0008others(1): Show | 6 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-7550dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42610011 | |||||
chr3:42610033
|
C | G | 94 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(91): Show | 109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.59-7537C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610033 | ||||||
chr3:42610074
|
C | T | 1 | a0001c0001t0003g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.59-7496C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610074 | ||||||
chr3:42610231
|
C | T | 22 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(19): Show | 25 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-7339C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610231 | ||||||
chr3:42610240
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-7330G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610240 | ||||||
chr3:42610286
|
G | A | 28 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(25): Show | 35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.59-7284G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610286 | ||||||
chr3:42610500
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.59-7070A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610500 | ||||||
chr3:42610545
|
T | A | 3 | a0003c0002t0007g0012a0003c0002t0007g0036a0003c0002t0007g0039 | 4 | HG01934.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-7025T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610545 | ||||||
chr3:42610594
|
A | AT | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.59-6966dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42610594 | |||||
chr3:42611050
|
A | G | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-6520A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611050 | ||||||
chr3:42611128
|
C | T | 1 | a0001c0001t0003g0020 | 2 | HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.59-6442C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611128 | ||||||
chr3:42611182
|
A | G | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-6388A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611182 | ||||||
chr3:42611224
|
G | A | 6 | a0002c0004t0006g0014a0002c0004t0006g0060a0002c0004t0006g0062others(3): Show | 6 | HG00280.hp1 HG01106.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-6346G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611224 | ||||||
chr3:42611354
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.59-6216A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611354 | ||||||
chr3:42611377
|
C | A | 3 | a0005c0006t0013g0082a0005c0006t0019g0008a0005c0006t0019g0083 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-6193C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611377 | ||||||
chr3:42611687
|
C | G | 1 | a0001c0013t0059g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.59-5883C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611687 | ||||||
chr3:42611732
|
C | CA | 130 | a0001c0001t0001g0242a0001c0001t0002g0224a0001c0001t0002g0253others(127): Show | 150 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.59-5821dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42611732 | |||||
chr3:42611750
|
T | A | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59-5820T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611750 | ||||||
chr3:42611890
|
A | G | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59-5680A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611890 | ||||||
chr3:42611916
|
C | T | 1 | a0001c0001t0048g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.59-5654C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611916 | ||||||
chr3:42611978
|
A | G | 1 | a0001c0001t0004g0100 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.59-5592A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611978 | ||||||
chr3:42612082
|
C | G | 1 | a0001c0001t0009g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59-5488C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612082 | ||||||
chr3:42612086
|
G | A | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-5484G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612086 | ||||||
chr3:42612087
|
C | T | 2 | a0002c0004t0015g0057a0002c0004t0047g0058 | 2 | HG00639.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.59-5483C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612087 | ||||||
chr3:42612164
|
G | A | 171 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(168): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-5406G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612164 | ||||||
chr3:42612230
|
A | T | 23 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(20): Show | 26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-5340A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612230 | ||||||
chr3:42612233
|
T | TTTGCTTG others(10): Show |
1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.59-5336_59-5320dup others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42612233 | |||||
chr3:42612327
|
T | C | 1 | a0001c0001t0010g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-5243T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612327 | ||||||
chr3:42612354
|
C | T | 1 | a0001c0001t0008g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.59-5216C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612354 | ||||||
chr3:42612366
|
T | A | 171 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(168): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-5204T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612366 | ||||||
chr3:42612405
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.59-5165A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612405 | ||||||
chr3:42612418
|
A | G | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.59-5152A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612418 | ||||||
chr3:42612460
|
A | G | 1 | a0001c0012t0001g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.59-5110A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612460 | ||||||
chr3:42612640
|
A | G | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.59-4930A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612640 | ||||||
chr3:42612652
|
A | G | 1 | a0001c0001t0013g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.59-4918A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612652 | ||||||
chr3:42612676
|
T | C | 1 | a0001c0001t0003g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.59-4894T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612676 | ||||||
chr3:42612725
|
A | G | 1 | a0001c0001t0027g0231 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59-4845A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612725 | ||||||
chr3:42612730
|
A | G | 8 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0112others(5): Show | 9 | HG00423.hp2 HG00597.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-4840A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612730 | ||||||
chr3:42612748
|
T | A | 1 | a0001c0001t0010g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-4822T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612748 | ||||||
chr3:42612799
|
G | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-4771G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612799 | ||||||
chr3:42612853
|
G | A | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-4717G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612853 | ||||||
chr3:42612891
|
G | A | 1 | a0002c0004t0015g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.59-4679G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612891 | ||||||
chr3:42612909
|
A | G | 1 | a0001c0001t0008g0174 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.59-4661A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612909 | ||||||
chr3:42613044
|
TAAC | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-4525_59-4523del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613044 | ||||||
chr3:42613160
|
C | T | 2 | a0001c0001t0046g0084a0001c0001t0052g0085 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.59-4410C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613160 | ||||||
chr3:42613554
|
A | G | 171 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(168): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-4016A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613554 | ||||||
chr3:42613601
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.59-3969A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613601 | ||||||
chr3:42613942
|
T | C | 4 | a0001c0001t0018g0145a0001c0001t0018g0147a0001c0001t0018g0148others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3628T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613942 | ||||||
chr3:42615082
|
C | CT | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-2474dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42615082 | |||||
chr3:42615086
|
T | G | 98 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(95): Show | 115 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.59-2484T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615086 | ||||||
chr3:42615266
|
A | G | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-2304A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615266 | ||||||
chr3:42615360
|
T | G | 1 | a0001c0001t0010g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-2210T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615360 | ||||||
chr3:42615379
|
G | A | 5 | a0001c0001t0001g0078a0001c0001t0001g0194a0001c0001t0001g0206others(2): Show | 5 | HG01070.hp2 HG01123.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-2191G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615379 | ||||||
chr3:42615382
|
A | AT | 7 | a0001c0001t0001g0189a0001c0001t0061g0276a0001c0008t0024g0292others(4): Show | 7 | HG01109.hp2 NA18967.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-2171dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42615382 | |||||
chr3:42615618
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-1952C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615618 | ||||||
chr3:42615732
|
G | T | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-1838G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615732 | ||||||
chr3:42615866
|
T | G | 94 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(91): Show | 109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.59-1704T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615866 | ||||||
chr3:42615905
|
CCTGCTTG others(5): Show |
C | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-1662_59-1651del others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42615905 | |||||
chr3:42615961
|
C | G | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-1609C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615961 | ||||||
chr3:42616176
|
G | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-1394G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616176 | ||||||
chr3:42616329
|
G | A | 1 | a0003c0002t0028g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.59-1241G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616329 | ||||||
chr3:42616349
|
G | A | 9 | a0002c0003t0014g0066a0002c0003t0017g0004a0002c0003t0017g0077others(6): Show | 9 | HG00558.hp1 HG02300.hp1 NA19011.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-1221G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616349 | ||||||
chr3:42616463
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.59-1107T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616463 | ||||||
chr3:42616692
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-878G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616692 | ||||||
chr3:42616764
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.59-806A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616764 | ||||||
chr3:42616825
|
T | C | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-745T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616825 | ||||||
chr3:42616915
|
C | T | 1 | a0003c0002t0014g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-655C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616915 | ||||||
chr3:42617080
|
T | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0202a0001c0001t0002g0246 | 3 | NA18950.hp2 NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.59-490T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617080 | ||||||
chr3:42617274
|
A | G | 1 | a0001c0001t0005g0273 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.59-296A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617274 | ||||||
chr3:42617282
|
A | G | 2 | a0003c0002t0016g0048a0003c0019t0016g0049 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.59-288A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617282 | ||||||
chr3:42617391
|
A | C | 2 | a0001c0001t0034g0144a0001c0001t0034g0146 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.59-179A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617391 | ||||||
chr3:42617774
|
T | TA | 31 | a0001c0001t0009g0135a0003c0002t0006g0045a0003c0002t0006g0046others(28): Show | 38 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.133+131dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42617774 | |||||
chr3:42617856
|
AAG | A | 3 | a0001c0001t0009g0010a0001c0001t0011g0010a0001c0001t0011g0128 | 4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+217_133+218del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42617856 | |||||
chr3:42618207
|
C | T | 4 | a0001c0001t0002g0169a0001c0001t0002g0173a0001c0001t0002g0175others(1): Show | 4 | NA18961.hp1 NA18963.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+563C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618207 | ||||||
chr3:42618282
|
C | T | 65 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(62): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.133+638C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618282 | ||||||
chr3:42618307
|
C | T | 1 | a0003c0002t0028g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.133+663C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618307 | ||||||
chr3:42618349
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.134-671C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618349 | ||||||
chr3:42618351
|
C | CA | 37 | a0001c0001t0002g0179a0001c0001t0002g0224a0001c0001t0005g0266others(34): Show | 40 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.134-650dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618351 | |||||
chr3:42618351
|
CA | C | 18 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(15): Show | 20 | HG01243.hp1 HG02109.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-650delA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618351 | |||||
chr3:42618371
|
T | A | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.134-649T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618371 | ||||||
chr3:42618411
|
A | G | 94 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(91): Show | 109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.134-609A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618411 | ||||||
chr3:42618462
|
C | T | 65 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(62): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.134-558C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618462 | ||||||
chr3:42618696
|
G | A | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.134-324G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618696 | ||||||
chr3:42618736
|
G | A | 1 | a0001c0001t0010g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.134-284G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618736 | ||||||
chr3:42618789
|
T | C | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.134-231T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618789 | ||||||
chr3:42618838
|
G | T | 320 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0078others(317): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.134-182G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618838 | ||||||
chr3:42618857
|
C | T | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.134-163C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618857 | ||||||
chr3:42618884
|
T | TGTCATCT others(353): Show |
1 | a0001c0001t0003g0109 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.134-122_134-121ins others(360): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618884 | |||||
chr3:42618997
|
C | CT | 14 | a0001c0001t0001g0188a0001c0001t0001g0223a0001c0001t0001g0234others(11): Show | 15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.134-5dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618997 | |||||
chr3:42618997
|
CT | C | 32 | a0001c0001t0002g0208a0001c0001t0003g0081a0003c0002t0006g0045others(29): Show | 39 | HG01070.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.134-5delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618997 | |||||
chr3:42618997
|
CTT | C | 34 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(31): Show | 37 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.134-6_134-5delTT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618997 | |||||
chr3:42619015
|
T | C | 1 | a0003c0002t0056g0043 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.134-5T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42619015 | ||||||
chr3:42619164
|
A | T | 1 | a0001c0001t0003g0097 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.241+37A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/16 | chr3 | 42619164 | ||||||
chr3:42619370
|
C | T | 11 | a0001c0001t0001g0189a0001c0001t0002g0215a0001c0001t0008g0030others(8): Show | 11 | HG00099.hp2 HG00738.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+243C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/16 | chr3 | 42619370 | ||||||
chr3:42619583
|
G | A | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.242-81G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/16 | chr3 | 42619583 | ||||||
chr3:42619820
|
T | A | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+112T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619820 | ||||||
chr3:42619867
|
A | G | 2 | a0001c0001t0003g0019a0001c0001t0011g0019 | 2 | NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.286+159A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619867 | ||||||
chr3:42619917
|
A | T | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+209A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619917 | ||||||
chr3:42619918
|
T | A | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+210T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619918 | ||||||
chr3:42619919
|
G | T | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+211G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619919 | ||||||
chr3:42620088
|
T | A | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+380T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620088 | ||||||
chr3:42620090
|
G | C | 1 | a0002c0004t0015g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.286+382G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620090 | ||||||
chr3:42620126
|
A | T | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+418A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620126 | ||||||
chr3:42620283
|
A | G | 4 | a0001c0001t0018g0145a0001c0001t0018g0147a0001c0001t0018g0148others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+575A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620283 | ||||||
chr3:42620542
|
T | C | 4 | a0001c0001t0009g0010a0001c0001t0010g0124a0001c0001t0011g0010others(1): Show | 5 | HG01074.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+834T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620542 | ||||||
chr3:42620584
|
T | G | 1 | a0016c0014t0025g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.287-845T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620584 | ||||||
chr3:42620902
|
G | A | 3 | a0005c0006t0013g0082a0005c0006t0019g0008a0005c0006t0019g0083 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-527G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620902 | ||||||
chr3:42621001
|
C | T | 28 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(25): Show | 35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-428C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42621001 | ||||||
chr3:42621079
|
G | A | 1 | a0001c0001t0002g0203 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.287-350G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42621079 | ||||||
chr3:42621660
|
T | C | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.374+144T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42621660 | ||||||
chr3:42621758
|
G | A | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.374+242G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42621758 | ||||||
chr3:42622306
|
A | G | 2 | a0001c0001t0009g0135a0001c0001t0011g0134 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.374+790A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622306 | ||||||
chr3:42622410
|
A | G | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.374+894A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622410 | ||||||
chr3:42622451
|
T | A | 99 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(96): Show | 116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.374+935T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622451 | ||||||
chr3:42622616
|
T | C | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.374+1100T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622616 | ||||||
chr3:42622868
|
C | T | 1 | a0002c0004t0006g0060 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.374+1352C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622868 | ||||||
chr3:42623047
|
C | T | 1 | a0001c0001t0003g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.374+1531C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623047 | ||||||
chr3:42623248
|
T | G | 1 | a0015c0022t0004g0101 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.374+1732T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623248 | ||||||
chr3:42623340
|
T | A | 1 | a0001c0001t0009g0092 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.374+1824T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623340 | ||||||
chr3:42623448
|
T | G | 1 | a0001c0001t0005g0273 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.374+1932T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623448 | ||||||
chr3:42623496
|
T | G | 1 | a0001c0001t0008g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.374+1980T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623496 | ||||||
chr3:42623753
|
C | T | 5 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0284others(2): Show | 5 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+2237C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623753 | ||||||
chr3:42623786
|
G | T | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.374+2270G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623786 | ||||||
chr3:42623853
|
A | T | 6 | a0001c0001t0003g0130a0004c0005t0010g0011a0004c0005t0010g0129others(3): Show | 7 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+2337A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623853 | ||||||
chr3:42624105
|
A | G | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.374+2589A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624105 | ||||||
chr3:42624138
|
G | A | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.374+2622G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624138 | ||||||
chr3:42624326
|
A | G | 1 | a0005c0006t0013g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.374+2810A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624326 | ||||||
chr3:42624463
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.374+2947A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624463 | ||||||
chr3:42624571
|
A | G | 1 | a0002c0004t0015g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.374+3055A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624571 | ||||||
chr3:42624666
|
A | G | 2 | a0001c0001t0003g0110a0001c0001t0004g0111 | 2 | NA18975.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.374+3150A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624666 | ||||||
chr3:42624836
|
C | T | 1 | a0001c0001t0008g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.374+3320C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624836 | ||||||
chr3:42624987
|
T | C | 3 | a0005c0006t0013g0082a0005c0006t0019g0008a0005c0006t0019g0083 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+3471T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624987 | ||||||
chr3:42624996
|
A | G | 65 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(62): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.374+3480A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624996 | ||||||
chr3:42625226
|
C | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.374+3710C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625226 | ||||||
chr3:42625278
|
C | A | 1 | a0001c0001t0010g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.374+3762C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625278 | ||||||
chr3:42625425
|
A | G | 1 | a0003c0002t0007g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.374+3909A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625425 | ||||||
chr3:42625441
|
T | TAAG | 68 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(65): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.374+3926_374+3928d others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42625441 | |||||
chr3:42625609
|
G | A | 5 | a0001c0001t0003g0132a0001c0001t0009g0125a0001c0001t0009g0127others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+4093G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625609 | ||||||
chr3:42625619
|
T | A | 2 | a0001c0001t0034g0144a0001c0001t0034g0146 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.374+4103T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625619 | ||||||
chr3:42625714
|
T | G | 6 | a0002c0004t0015g0054a0002c0004t0015g0055a0002c0004t0015g0056others(3): Show | 6 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.374+4198T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625714 | ||||||
chr3:42626052
|
C | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.375-4494C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626052 | ||||||
chr3:42626123
|
T | C | 2 | a0001c0001t0003g0094a0001c0001t0003g0140 | 2 | NA18985.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.375-4423T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626123 | ||||||
chr3:42626167
|
A | AT | 27 | a0001c0001t0001g0194a0001c0001t0001g0223a0001c0001t0003g0130others(24): Show | 30 | HG01074.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.375-4367dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42626167 | |||||
chr3:42626167
|
A | ATT | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.375-4368_375-4367d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42626167 | |||||
chr3:42626234
|
TATTC | T | 4 | a0001c0001t0018g0145a0001c0001t0018g0147a0001c0001t0018g0148others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.375-4309_375-4306d others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42626234 | |||||
chr3:42626444
|
A | G | 62 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0027others(59): Show | 63 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.375-4102A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626444 | ||||||
chr3:42626949
|
A | G | 99 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(96): Show | 116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.375-3597A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626949 | ||||||
chr3:42627022
|
C | T | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.375-3524C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627022 | ||||||
chr3:42627534
|
G | T | 1 | a0003c0002t0007g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.375-3012G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627534 | ||||||
chr3:42627608
|
A | G | 1 | a0001c0001t0030g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.375-2938A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627608 | ||||||
chr3:42627630
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.375-2916A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627630 | ||||||
chr3:42627901
|
A | G | 68 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(65): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.375-2645A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627901 | ||||||
chr3:42627968
|
T | C | 68 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(65): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.375-2578T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627968 | ||||||
chr3:42628144
|
A | T | 1 | a0001c0001t0001g0242 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.375-2402A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628144 | ||||||
chr3:42628176
|
T | C | 1 | a0001c0001t0003g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.375-2370T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628176 | ||||||
chr3:42628198
|
G | C | 3 | a0001c0001t0009g0010a0001c0001t0011g0010a0001c0001t0011g0128 | 4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.375-2348G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628198 | ||||||
chr3:42628277
|
C | T | 8 | a0003c0002t0007g0012a0003c0002t0007g0036a0003c0002t0007g0037others(5): Show | 9 | HG01192.hp1 HG01934.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.375-2269C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628277 | ||||||
chr3:42628280
|
G | A | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.375-2266G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628280 | ||||||
chr3:42628389
|
C | T | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.375-2157C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628389 | ||||||
chr3:42628573
|
C | T | 1 | a0001c0008t0024g0292 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.375-1973C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628573 | ||||||
chr3:42628727
|
T | C | 68 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(65): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.375-1819T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628727 | ||||||
chr3:42628737
|
C | T | 1 | a0001c0001t0010g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.375-1809C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628737 | ||||||
chr3:42628786
|
G | A | 1 | a0002c0004t0015g0055 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.375-1760G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628786 | ||||||
chr3:42628856
|
G | A | 65 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(62): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.375-1690G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628856 | ||||||
chr3:42628957
|
A | G | 167 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(164): Show | 194 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.375-1589A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628957 | ||||||
chr3:42629475
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.375-1071G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42629475 | ||||||
chr3:42629567
|
G | A | 1 | a0001c0012t0001g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.375-979G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42629567 | ||||||
chr3:42630122
|
C | G | 1 | a0001c0001t0060g0289 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.375-424C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630122 | ||||||
chr3:42630170
|
C | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.375-376C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630170 | ||||||
chr3:42630176
|
T | G | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.375-370T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630176 | ||||||
chr3:42630362
|
AGTAAGAT others(7): Show |
A | 1 | a0001c0001t0004g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.375-183_375-170del others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630362 | ||||||
chr3:42630681
|
T | A | 1 | a0001c0001t0010g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404+106T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630681 | ||||||
chr3:42630730
|
T | A | 3 | a0001c0001t0009g0010a0001c0001t0011g0010a0001c0001t0011g0128 | 4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+155T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630730 | ||||||
chr3:42630761
|
G | T | 1 | a0001c0001t0005g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.404+186G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630761 | ||||||
chr3:42630994
|
G | A | 66 | a0001c0001t0001g0220a0002c0003t0006g0006a0002c0003t0006g0015others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.405-177G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630994 | ||||||
chr3:42631490
|
T | C | 68 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(65): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.550+174T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631490 | ||||||
chr3:42631762
|
A | G | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.550+446A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631762 | ||||||
chr3:42631794
|
T | C | 1 | a0001c0001t0002g0279 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.550+478T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631794 | ||||||
chr3:42631987
|
C | T | 65 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(62): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.551-614C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631987 | ||||||
chr3:42632061
|
C | CT | 23 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0001g0188others(20): Show | 24 | HG00544.hp2 HG01109.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.551-515dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | |||||
chr3:42632061
|
CT | C | 9 | a0001c0001t0001g0206a0001c0001t0005g0251a0001c0001t0009g0135others(6): Show | 9 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.551-515delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | |||||
chr3:42632061
|
CTT | C | 12 | a0001c0001t0003g0105a0001c0001t0004g0111a0001c0001t0004g0139others(9): Show | 12 | HG02723.hp2 HG02809.hp2 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.551-516_551-515del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | |||||
chr3:42632061
|
CTTT | C | 116 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(113): Show | 136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.551-517_551-515del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | |||||
chr3:42632404
|
G | C | 97 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(94): Show | 114 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.551-197G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42632404 | ||||||
chr3:42632536
|
A | AT | 30 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(27): Show | 37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.551-59dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632536 | |||||
chr3:42632836
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.773+13C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42632836 | ||||||
chr3:42632967
|
A | G | 12 | a0001c0001t0002g0183a0001c0001t0002g0222a0001c0001t0002g0224others(9): Show | 12 | HG01358.hp1 HG01496.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.773+144A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42632967 | ||||||
chr3:42633279
|
C | T | 1 | a0002c0003t0042g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.774-301C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42633279 | ||||||
chr3:42633560
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.774-20G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42633560 | ||||||
chr3:42633788
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.929+53G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42633788 | ||||||
chr3:42633993
|
T | C | 1 | a0001c0001t0021g0198 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.929+258T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42633993 | ||||||
chr3:42634117
|
T | C | 2 | a0001c0001t0030g0086a0001c0001t0030g0087 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.929+382T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634117 | ||||||
chr3:42634284
|
T | G | 1 | a0003c0002t0028g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.930-329T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634284 | ||||||
chr3:42634357
|
C | T | 1 | a0001c0001t0010g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.930-256C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634357 | ||||||
chr3:42634367
|
T | A | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.930-246T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634367 | ||||||
chr3:42634773
|
G | T | 68 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(65): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1017+73G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | chr3 | 42634773 | ||||||
chr3:42634933
|
G | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1017+233G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | chr3 | 42634933 | ||||||
chr3:42635054
|
A | T | 2 | a0001c0001t0034g0144a0001c0001t0034g0146 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1018-167A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | chr3 | 42635054 | ||||||
chr3:42635057
|
TA | T | 6 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0270others(3): Show | 6 | HG01516.hp1 HG03017.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-143delA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | |||||
chr3:42635057
|
TAA | T | 67 | a0001c0001t0009g0135a0001c0001t0011g0134a0001c0001t0018g0145others(64): Show | 75 | HG00280.hp1 HG00597.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-144_1018-143d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | |||||
chr3:42635057
|
TAAA | T | 9 | a0001c0001t0003g0088a0002c0003t0006g0006a0002c0003t0006g0069others(6): Show | 11 | HG00558.hp1 HG00639.hp2 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.1018-145_1018-143d others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | |||||
chr3:42635057
|
TAAAA | T | 89 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(86): Show | 106 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1018-146_1018-143d others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | |||||
chr3:42635433
|
C | A | 65 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(62): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1163+67C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635433 | ||||||
chr3:42635442
|
A | G | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1163+76A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635442 | ||||||
chr3:42635561
|
G | A | 1 | a0003c0002t0007g0012 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1163+195G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635561 | ||||||
chr3:42635658
|
G | A | 258 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(255): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1163+292G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635658 | ||||||
chr3:42635695
|
G | A | 1 | a0001c0007t0029g0171 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1163+329G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635695 | ||||||
chr3:42635796
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1163+430A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635796 | ||||||
chr3:42635862
|
C | T | 68 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(65): Show | 80 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1163+496C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635862 | ||||||
chr3:42635863
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1163+497G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635863 | ||||||
chr3:42635907
|
C | CA | 8 | a0001c0001t0001g0194a0001c0007t0005g0159a0001c0007t0005g0176others(5): Show | 8 | HG00099.hp2 HG01192.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163+556dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 42635907 | |||||
chr3:42635920
|
A | T | 2 | a0001c0001t0004g0121a0001c0001t0004g0123 | 2 | NA18990.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1163+554A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635920 | ||||||
chr3:42636011
|
C | T | 2 | a0001c0001t0004g0099a0001c0001t0004g0100 | 2 | HG01257.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1163+645C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636011 | ||||||
chr3:42636090
|
C | T | 1 | a0001c0001t0004g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1163+724C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636090 | ||||||
chr3:42636344
|
T | C | 171 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(168): Show | 198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.1164-524T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636344 | ||||||
chr3:42636406
|
C | T | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1164-462C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636406 | ||||||
chr3:42636422
|
A | G | 22 | a0003c0002t0006g0045a0003c0002t0006g0046a0003c0002t0006g0047others(19): Show | 28 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.1164-446A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636422 | ||||||
chr3:42636653
|
TA | T | 6 | a0002c0004t0015g0054a0002c0004t0015g0055a0002c0004t0015g0056others(3): Show | 6 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164-205delA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 42636653 | |||||
chr3:42639789
|
GTC | G | 3 | a0005c0006t0013g0082a0005c0006t0019g0008a0005c0006t0019g0083 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4046+41_4046+42del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 42639789 | |||||
chr3:42639859
|
G | A | 35 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(32): Show | 38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.4046+109G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42639859 | ||||||
chr3:42639895
|
G | A | 65 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(62): Show | 75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.4046+145G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42639895 | ||||||
chr3:42639953
|
A | ACT | 165 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(162): Show | 192 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.4046+204_4046+205d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 42639953 | |||||
chr3:42639960
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4046+210C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42639960 | ||||||
chr3:42640158
|
A | G | 3 | a0001c0001t0005g0212a0001c0001t0005g0213a0001c0001t0005g0225 | 3 | HG00738.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.4046+408A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640158 | ||||||
chr3:42640300
|
C | G | 1 | a0001c0001t0004g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4046+550C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640300 | ||||||
chr3:42640301
|
T | C | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4046+551T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640301 | ||||||
chr3:42640630
|
A | G | 1 | a0002c0003t0023g0073 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4046+880A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640630 | ||||||
chr3:42640632
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0211a0001c0001t0001g0221 | 3 | NA18966.hp1 NA18991.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.4046+882C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640632 | ||||||
chr3:42640696
|
C | T | 68 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(65): Show | 80 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.4046+946C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640696 | ||||||
chr3:42640755
|
G | T | 1 | a0001c0008t0024g0294 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4046+1005G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640755 | ||||||
chr3:42640839
|
C | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0220 | 2 | HG02055.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4046+1089C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640839 | ||||||
chr3:42640843
|
T | C | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4046+1093T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640843 | ||||||
chr3:42641052
|
G | A | 63 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(60): Show | 73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.4046+1302G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641052 | ||||||
chr3:42641092
|
C | T | 1 | a0001c0001t0029g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4046+1342C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641092 | ||||||
chr3:42641197
|
AG | A | 4 | a0001c0001t0018g0145a0001c0001t0018g0147a0001c0001t0018g0148others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4047-1302delG | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 42641197 | |||||
chr3:42641403
|
T | C | 1 | a0003c0002t0035g0013 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4047-1098T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641403 | ||||||
chr3:42641618
|
A | G | 313 | a0001c0001t0001g0031a0001c0001t0001g0078a0001c0001t0001g0143others(310): Show | 344 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.4047-883A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641618 | ||||||
chr3:42641627
|
C | A | 62 | a0002c0003t0006g0006a0002c0003t0006g0015a0002c0003t0006g0069others(59): Show | 72 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.4047-874C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641627 | ||||||
chr3:42641631
|
G | A | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.4047-870G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641631 | ||||||
chr3:42641646
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.4047-855G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641646 | ||||||
chr3:42641677
|
A | C | 2 | a0001c0001t0009g0285a0001c0001t0009g0286 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4047-824A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641677 | ||||||
chr3:42641735
|
G | A | 1 | a0001c0001t0005g0251 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4047-766G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641735 | ||||||
chr3:42641750
|
T | C | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4047-751T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641750 | ||||||
chr3:42641890
|
A | T | 2 | a0008c0011t0026g0287a0008c0011t0026g0288 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4047-611A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641890 | ||||||
chr3:42641927
|
T | C | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4047-574T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641927 | ||||||
chr3:42641960
|
C | T | 1 | a0003c0002t0028g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4047-541C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641960 | ||||||
chr3:42642059
|
T | C | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4047-442T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42642059 | ||||||
chr3:42642407
|
G | C | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.4047-94G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42642407 | ||||||
chr3:42642641
|
A | G | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4142+45A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42642641 | ||||||
chr3:42642770
|
C | T | 1 | a0001c0001t0003g0020 | 2 | HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.4142+174C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42642770 | ||||||
chr3:42643034
|
C | T | 1 | a0001c0001t0010g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4143-305C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42643034 | ||||||
chr3:42643093
|
C | T | 6 | a0003c0002t0016g0005a0003c0002t0016g0048a0003c0002t0031g0005others(3): Show | 7 | HG02622.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4143-246C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42643093 | ||||||
chr3:42643295
|
G | A | 66 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294others(63): Show | 76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4143-44G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42643295 | ||||||
chr3:42643542
|
C | T | 4 | a0001c0001t0018g0145a0001c0001t0018g0147a0001c0001t0018g0148others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4199+147C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 15/16 | chr3 | 42643542 | ||||||
chr3:42643874
|
T | C | 1 | a0003c0002t0028g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4200-28T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 15/16 | chr3 | 42643874 | ||||||
chr3:42644033
|
C | T | 2 | a0003c0002t0023g0040a0003c0002t0023g0041 | 2 | HG01192.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4301+30C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644033 | ||||||
chr3:42644226
|
C | T | 4 | a0001c0001t0009g0010a0001c0001t0010g0124a0001c0001t0011g0010others(1): Show | 5 | HG01074.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.4301+223C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644226 | ||||||
chr3:42644324
|
A | G | 99 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(96): Show | 116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.4301+321A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644324 | ||||||
chr3:42644349
|
AT | A | 6 | a0001c0001t0003g0130a0004c0005t0010g0011a0004c0005t0010g0129others(3): Show | 7 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4301+354delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 42644349 | |||||
chr3:42644419
|
A | G | 79 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0024others(76): Show | 80 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.4301+416A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644419 | ||||||
chr3:42644468
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4301+465A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644468 | ||||||
chr3:42644509
|
C | T | 94 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(91): Show | 109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.4301+506C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644509 | ||||||
chr3:42644658
|
A | G | 3 | a0001c0008t0024g0292a0001c0008t0024g0293a0001c0008t0024g0294 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.4301+655A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644658 | ||||||
chr3:42644671
|
G | C | 1 | a0001c0001t0001g0221 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4301+668G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644671 | ||||||
chr3:42644771
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4301+768A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644771 | ||||||
chr3:42644978
|
T | TTG | 89 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0016others(86): Show | 102 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.4302-892_4302-891d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 42644978 | |||||
chr3:42644978
|
T | TTGTG | 5 | a0001c0001t0009g0285a0001c0001t0009g0286a0001c0001t0011g0009others(2): Show | 7 | HG01256.hp1 HG01891.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.4302-894_4302-891d others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 42644978 | |||||
chr3:42645208
|
A | T | 2 | a0003c0002t0057g0034a0003c0002t0058g0050 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4302-680A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645208 | ||||||
chr3:42645407
|
G | A | 1 | a0001c0001t0008g0237 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4302-481G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645407 | ||||||
chr3:42645752
|
A | G | 5 | a0001c0001t0001g0234a0001c0001t0001g0248a0001c0001t0001g0260others(2): Show | 5 | NA18747.hp2 NA18970.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.4302-136A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645752 | ||||||
chr3:42645786
|
C | T | 79 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0024others(76): Show | 80 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.4302-102C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645786 |