Item | Value |
---|---|
geneid | 317649 |
ensemblid | ENSG00000163412.13 |
hgncid | 31837 |
symbol | EIF4E3 |
name | eukaryotic translation initiation factor 4E family member 3 |
refseq_nuc | NM_001134651.2 |
refseq_prot | NP_001128123.1 |
ensembl_nuc | ENST00000425534.8 |
ensembl_prot | ENSP00000393324.2 |
mane_status | MANE Select |
chr | chr3 |
start | 71675414 |
end | 71725402 |
strand | - |
ver | v1.2 |
region | chr3:71675414-71725402 |
region5000 | chr3:71670414-71730402 |
regionname0 | EIF4E3_chr3_71675414_71725402 |
regionname5000 | EIF4E3_chr3_71670414_71730402 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 224 | 397 | 94 | 78 | 169 | 12 | 42 | 129 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | MALPP others(219): Show |
chr3 | 71670414 | 71730402 |
a0002 | 0/0 | 224 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | MALPP others(219): Show |
chr3 | 71670414 | 71730402 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 672 | 396 | 94 | 78 | 169 | 12 | 41 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | ATGGC others(667): Show |
chr3 | 71670414 | 71730402 | ||
a0001c0003 | 0/0 | 672 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | ATGGC others(667): Show |
chr3 | 71670414 | 71730402 | ||
a0002c0002 | 0/0 | 672 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | ATGGC others(667): Show |
chr3 | 71670414 | 71730402 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9978 | 126 | 31 | 37 | 32 | 6 | 19 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0002 | 0/0 | 9979 | 60 | 3 | 5 | 46 | 2 | 4 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0003 | 0/0 | 9979 | 53 | 22 | 3 | 26 | 0 | 2 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0004 | 0/0 | 9979 | 30 | 0 | 14 | 16 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0005 | 0/0 | 9979 | 13 | 3 | 0 | 4 | 1 | 5 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0006 | 0/0 | 9979 | 8 | 6 | 2 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0007 | 0/0 | 9980 | 5 | 0 | 0 | 5 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9975): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0008 | 0/0 | 9978 | 5 | 5 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0009 | 0/0 | 9978 | 4 | 0 | 3 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0010 | 0/0 | 9979 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0011 | 0/0 | 9979 | 3 | 0 | 3 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0012 | 0/0 | 9980 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9975): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0013 | 0/0 | 9978 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0014 | 0/0 | 9978 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0015 | 0/0 | 9978 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0016 | 0/0 | 9979 | 2 | 0 | 1 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0017 | 0/0 | 9979 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0018 | 0/0 | 9979 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0019 | 0/0 | 9979 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0020 | 0/0 | 9979 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0021 | 0/0 | 9979 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0022 | 0/0 | 9979 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0023 | 0/0 | 9979 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0024 | 0/0 | 9980 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9975): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0025 | 0/0 | 9979 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0026 | 0/0 | 9980 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9975): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0027 | 0/0 | 9978 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0028 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0029 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0030 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0031 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0032 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0033 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0034 | 0/0 | 9978 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0035 | 0/0 | 9978 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0036 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0037 | 0/0 | 9978 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0038 | 0/0 | 9978 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0039 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0040 | 0/0 | 9978 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0041 | 0/1 | 9978 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0042 | 0/0 | 9978 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0043 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0044 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0045 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0046 | 0/0 | 9977 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9972): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0047 | 0/0 | 9978 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0048 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0049 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0050 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0051 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0052 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0053 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0054 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0055 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0056 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0057 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0058 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0059 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0060 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0061 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0062 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0063 | 0/0 | 9978 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0064 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0065 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0066 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0067 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0068 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0069 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0070 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0071 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0072 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0073 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0074 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0075 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0076 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0077 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0078 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0079 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9974): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0080 | 0/0 | 9980 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9975): Show |
chr3 | 71670414 | 71730402 |
a0001c0001t0081 | 0/0 | 9980 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9975): Show |
chr3 | 71670414 | 71730402 |
a0001c0003t0001 | 0/0 | 9978 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9973): Show |
chr3 | 71670414 | 71730402 |
a0002c0002t0007 | 0/0 | 9980 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | GCGCG others(9975): Show |
chr3 | 71670414 | 71730402 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0001 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0007g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0009g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0009g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0009g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0009g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0011g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0011g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0011g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0012g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0014g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0015g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0016g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0016g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0017g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0017g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0018g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0018g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0019g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0019g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0020g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0020g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0021g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0021g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0022g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0023g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0023g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0024g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0024g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0025g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0025g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0026g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0026g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0027g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0028g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0029g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0030g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0031g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0032g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0033g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0034g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0035g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0036g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0037g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0038g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0039g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0040g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0041g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0042g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0043g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0044g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0045g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0046g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0047g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0048g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0049g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0050g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0051g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0052g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0053g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0054g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0055g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0056g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0057g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0058g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0059g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0060g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0061g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0062g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0063g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0064g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0065g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0066g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0067g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0068g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0069g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0070g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0071g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0072g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0073g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0074g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0075g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0076g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0077g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0078g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0079g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0080g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0001t0081g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0001c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
a0002c0002t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | GBR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | GBR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0301 | EUR | FIN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00280 | hp2 | a0001 | c0001 | t0047 | g0067 | EUR | FIN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00423 | hp2 | a0001 | c0001 | t0007 | g0256 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00438 | hp1 | a0001 | c0001 | t0026 | g0091 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00544 | hp1 | a0001 | c0001 | t0042 | g0134 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00639 | hp2 | a0001 | c0001 | t0040 | g0186 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00642 | hp2 | a0001 | c0001 | t0011 | g0109 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00733 | hp1 | a0001 | c0001 | t0016 | g0341 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00738 | hp1 | a0001 | c0001 | t0058 | g0226 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01070 | hp2 | a0001 | c0001 | t0021 | g0224 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01071 | hp1 | a0001 | c0001 | t0021 | g0225 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01074 | hp2 | a0001 | c0001 | t0009 | g0345 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01081 | hp1 | a0001 | c0001 | t0011 | g0097 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01081 | hp2 | a0001 | c0001 | t0009 | g0344 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01106 | hp2 | a0001 | c0001 | t0037 | g0273 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0124 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01169 | hp2 | a0001 | c0001 | t0067 | g0334 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0362 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01192 | hp2 | a0001 | c0001 | t0054 | g0168 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0321 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0366 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01433 | hp2 | a0001 | c0001 | t0011 | g0065 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0137 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01515 | hp1 | a0001 | c0001 | t0035 | g0343 | EUR | IBS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | IBS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0342 | EUR | IBS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0359 | EUR | IBS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | IBS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0356 | EUR | IBS | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01884 | hp1 | a0001 | c0001 | t0013 | g0064 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01934 | hp1 | a0001 | c0001 | t0053 | g0169 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01975 | hp1 | a0001 | c0001 | t0063 | g0265 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0287 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01981 | hp2 | a0001 | c0001 | t0027 | g0171 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0222 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0165 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02055 | hp1 | a0001 | c0001 | t0080 | g0324 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02056 | hp1 | a0001 | c0001 | t0010 | g0170 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02071 | hp1 | a0001 | c0001 | t0012 | g0160 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02071 | hp2 | a0001 | c0001 | t0012 | g0212 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02083 | hp2 | a0001 | c0001 | t0062 | g0167 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02129 | hp1 | a0001 | c0001 | t0055 | g0145 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02129 | hp2 | a0001 | c0001 | t0017 | g0024 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02132 | hp1 | a0001 | c0001 | t0052 | g0031 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02135 | hp1 | a0001 | c0001 | t0059 | g0284 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CDX | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | CDX | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02257 | hp1 | a0001 | c0001 | t0032 | g0019 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02257 | hp2 | a0001 | c0001 | t0045 | g0303 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0232 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0300 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02451 | hp2 | a0001 | c0001 | t0028 | g0022 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02523 | hp1 | a0001 | c0001 | t0046 | g0205 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02572 | hp1 | a0001 | c0001 | t0039 | g0307 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0230 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02615 | hp1 | a0001 | c0001 | t0068 | g0309 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0327 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02647 | hp1 | a0001 | c0001 | t0029 | g0104 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02683 | hp1 | a0001 | c0001 | t0023 | g0295 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0302 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0330 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0316 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02818 | hp2 | a0001 | c0001 | t0044 | g0207 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02895 | hp1 | a0001 | c0001 | t0064 | g0196 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02897 | hp1 | a0001 | c0001 | t0022 | g0197 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02922 | hp1 | a0001 | c0001 | t0033 | g0193 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02922 | hp2 | a0001 | c0001 | t0066 | g0125 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0304 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0245 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0340 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0360 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0100 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0305 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0110 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0317 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0192 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03486 | hp1 | a0001 | c0001 | t0036 | g0323 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03490 | hp1 | a0001 | c0001 | t0069 | g0093 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0337 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03516 | hp2 | a0001 | c0001 | t0031 | g0361 | AFR | ESN | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03540 | hp2 | a0001 | c0001 | t0022 | g0085 | AFR | GWD | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03654 | hp1 | a0001 | c0001 | t0079 | g0338 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03669 | hp1 | a0001 | c0001 | t0081 | g0294 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03669 | hp2 | a0001 | c0001 | t0034 | g0276 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0206 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03710 | hp1 | a0001 | c0001 | t0078 | g0270 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0251 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03927 | hp2 | a0001 | c0001 | t0023 | g0296 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04115 | hp2 | a0001 | c0001 | t0072 | g0199 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04184 | hp1 | a0001 | c0001 | t0049 | g0094 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0203 | SAS | BEB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04204 | hp2 | a0001 | c0001 | t0070 | g0130 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04228 | hp1 | a0001 | c0001 | t0016 | g0108 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0364 | SAS | STU | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | YRI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | YRI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18941 | hp1 | a0001 | c0001 | t0019 | g0278 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0373 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18943 | hp2 | a0001 | c0001 | t0014 | g0248 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0372 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18944 | hp2 | a0001 | c0001 | t0077 | g0182 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18947 | hp1 | a0001 | c0001 | t0017 | g0073 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18951 | hp1 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0268 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0370 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18962 | hp1 | a0002 | c0002 | t0007 | g0173 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18963 | hp1 | a0001 | c0001 | t0010 | g0266 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18968 | hp2 | a0001 | c0001 | t0007 | g0367 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18977 | hp2 | a0001 | c0001 | t0019 | g0025 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18981 | hp1 | a0001 | c0001 | t0076 | g0219 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18981 | hp2 | a0001 | c0001 | t0075 | g0144 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0045 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18988 | hp2 | a0001 | c0001 | t0024 | g0132 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18991 | hp1 | a0001 | c0001 | t0012 | g0161 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18991 | hp2 | a0001 | c0001 | t0024 | g0047 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18998 | hp2 | a0001 | c0001 | t0018 | g0099 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19000 | hp2 | a0001 | c0001 | t0071 | g0216 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19003 | hp1 | a0001 | c0001 | t0014 | g0246 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19003 | hp2 | a0001 | c0001 | t0025 | g0095 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19011 | hp1 | a0001 | c0001 | t0051 | g0040 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19011 | hp2 | a0001 | c0001 | t0020 | g0078 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19012 | hp2 | a0001 | c0001 | t0056 | g0283 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19030 | hp1 | a0001 | c0001 | t0048 | g0113 | AFR | LWK | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19030 | hp2 | a0001 | c0001 | t0015 | g0331 | AFR | LWK | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19043 | hp1 | a0001 | c0001 | t0030 | g0020 | AFR | LWK | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0371 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19065 | hp1 | a0001 | c0001 | t0050 | g0187 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0374 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19068 | hp1 | a0001 | c0001 | t0060 | g0272 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19068 | hp2 | a0001 | c0001 | t0057 | g0147 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19070 | hp2 | a0001 | c0001 | t0018 | g0156 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19072 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19076 | hp1 | a0001 | c0001 | t0061 | g0080 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19082 | hp2 | a0001 | c0001 | t0026 | g0255 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19083 | hp1 | a0001 | c0001 | t0065 | g0058 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19084 | hp1 | a0001 | c0001 | t0038 | g0174 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19090 | hp1 | a0001 | c0001 | t0020 | g0079 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19091 | hp1 | a0001 | c0001 | t0025 | g0026 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA20752 | hp2 | a0001 | c0001 | t0009 | g0353 | EUR | TSI | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0363 | SAS | GIH | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | GIH | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | USA | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0069 | AFR | USA | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA20300 | hp1 | a0001 | c0001 | t0074 | g0328 | AFR | USA | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0068 | AFR | USA | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA21309 | hp1 | a0001 | c0001 | t0043 | g0351 | AFR | LWK | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
NA21309 | hp2 | a0001 | c0001 | t0073 | g0082 | AFR | LWK | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
homoSapiens | chm13v2 | a0001 | c0001 | t0041 | g0211 | REF | REF | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0335 | REF | REF | EIF4E3_chr3_71670414_71730402 | EIF4E3 | chr3 | 71670414 | 71730402 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:71693907 | A | G | 1 | a0002 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.440T>C | p.Ile147Thr | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/7 | 475/9978 | 440/675 | 147/224 | chr3 | 71693907 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:71693876 | T | C | 1 | a0001c0003 | 1 | HG03017.hp2 | splice_region_variant&synonymous_variant | LOW | c.471A>G | p.Ala157Ala | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/7 | 506/9978 | 471/675 | 157/224 | chr3 | 71693876 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:71675434 | T | A | 2 | a0001c0001t0021 a0001c0001t0032 |
3 | HG01070.hp2 HG01071.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9248A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 9248 | chr3 | 71675434 | ||||||
chr3:71675525 | C | T | 3 | a0001c0001t0010 a0001c0001t0062 a0001c0001t0063 |
5 | HG01975.hp1 HG02027.hp1 HG02056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9157G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 9157 | chr3 | 71675525 | ||||||
chr3:71675724 | T | C | 1 | a0001c0001t0018 | 2 | NA18998.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8958A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 8958 | chr3 | 71675724 | ||||||
chr3:71675992 | C | T | 1 | a0001c0001t0074 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8690G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 8690 | chr3 | 71675992 | ||||||
chr3:71675996 | G | C | 7 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0030 others(4): Show |
15 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*8686C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 8686 | chr3 | 71675996 | ||||||
chr3:71676003 | G | A | 1 | a0001c0001t0062 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8679C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 8679 | chr3 | 71676003 | ||||||
chr3:71676192 | A | G | 25 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(22): Show |
55 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*8490T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 8490 | chr3 | 71676192 | ||||||
chr3:71676225 | A | T | 14 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0017 others(11): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8457T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 8457 | chr3 | 71676225 | ||||||
chr3:71676343 | A | C | 1 | a0001c0001t0035 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8339T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 8339 | chr3 | 71676343 | ||||||
chr3:71676744 | TC | T | 5 | a0001c0001t0025 a0001c0001t0046 a0001c0001t0063 others(2): Show |
6 | HG01975.hp1 HG02523.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7937delG | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7937 | chr3 | 71676744 | ||||||
chr3:71676745 | C | T | 43 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(40): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*7937G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7937 | chr3 | 71676745 | ||||||
chr3:71676745 | CA | C | 3 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0075 |
7 | HG01081.hp2 HG02735.hp1 HG02735.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7936delT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7936 | chr3 | 71676745 | ||||||
chr3:71676746 | A | T | 5 | a0001c0001t0025 a0001c0001t0046 a0001c0001t0063 others(2): Show |
6 | HG01975.hp1 HG02523.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7936T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7936 | chr3 | 71676746 | ||||||
chr3:71676817 | T | G | 42 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(39): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*7865A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7865 | chr3 | 71676817 | ||||||
chr3:71676924 | C | A | 1 | a0001c0001t0011 | 3 | HG00642.hp2 HG01081.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7758G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7758 | chr3 | 71676924 | ||||||
chr3:71677108 | T | C | 47 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(44): Show |
140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*7574A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7574 | chr3 | 71677108 | ||||||
chr3:71677119 | T | G | 47 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(44): Show |
140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*7563A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7563 | chr3 | 71677119 | ||||||
chr3:71677122 | T | C | 1 | a0001c0001t0009 | 4 | HG01074.hp2 HG01081.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7560A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7560 | chr3 | 71677122 | ||||||
chr3:71677310 | G | A | 1 | a0001c0001t0065 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7372C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7372 | chr3 | 71677310 | ||||||
chr3:71677424 | G | A | 2 | a0001c0001t0006 a0001c0001t0066 |
9 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7258C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7258 | chr3 | 71677424 | ||||||
chr3:71677478 | T | G | 1 | a0001c0001t0075 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7204A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7204 | chr3 | 71677478 | ||||||
chr3:71677589 | A | G | 1 | a0001c0001t0056 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7093T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7093 | chr3 | 71677589 | ||||||
chr3:71677620 | T | C | 1 | a0001c0001t0015 | 2 | HG03098.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7062A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 7062 | chr3 | 71677620 | ||||||
chr3:71677812 | C | A | 1 | a0001c0001t0060 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6870G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6870 | chr3 | 71677812 | ||||||
chr3:71677834 | G | A | 1 | a0001c0001t0013 | 2 | HG01884.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6848C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6848 | chr3 | 71677834 | ||||||
chr3:71677865 | C | T | 2 | a0001c0001t0029 a0001c0001t0033 |
2 | HG02647.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6817G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6817 | chr3 | 71677865 | ||||||
chr3:71677902 | G | T | 1 | a0001c0001t0055 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6780C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6780 | chr3 | 71677902 | ||||||
chr3:71677953 | C | T | 1 | a0001c0001t0073 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6729G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6729 | chr3 | 71677953 | ||||||
chr3:71678082 | T | C | 1 | a0001c0001t0037 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6600A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6600 | chr3 | 71678082 | ||||||
chr3:71678295 | A | G | 1 | a0001c0001t0053 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6387T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6387 | chr3 | 71678295 | ||||||
chr3:71678317 | C | A | 1 | a0001c0001t0054 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6365G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6365 | chr3 | 71678317 | ||||||
chr3:71678338 | C | A | 1 | a0001c0001t0046 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6344G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6344 | chr3 | 71678338 | ||||||
chr3:71678538 | C | A | 15 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0010 others(12): Show |
40 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6144G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6144 | chr3 | 71678538 | ||||||
chr3:71678593 | A | G | 1 | a0001c0001t0034 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6089T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 6089 | chr3 | 71678593 | ||||||
chr3:71678691 | G | C | 1 | a0001c0001t0039 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5991C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5991 | chr3 | 71678691 | ||||||
chr3:71678913 | A | G | 2 | a0001c0001t0029 a0001c0001t0033 |
2 | HG02647.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5769T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5769 | chr3 | 71678913 | ||||||
chr3:71678914 | T | C | 41 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(38): Show |
135 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*5768A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5768 | chr3 | 71678914 | ||||||
chr3:71679042 | A | G | 2 | a0001c0001t0029 a0001c0001t0033 |
2 | HG02647.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5640T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5640 | chr3 | 71679042 | ||||||
chr3:71679092 | C | T | 1 | a0001c0001t0062 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5590G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5590 | chr3 | 71679092 | ||||||
chr3:71679146 | A | C | 1 | a0001c0001t0052 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5536T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5536 | chr3 | 71679146 | ||||||
chr3:71679319 | C | G | 1 | a0001c0001t0051 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5363G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5363 | chr3 | 71679319 | ||||||
chr3:71679344 | T | C | 1 | a0001c0001t0076 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5338A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5338 | chr3 | 71679344 | ||||||
chr3:71679522 | C | A | 1 | a0001c0001t0046 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5160G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5160 | chr3 | 71679522 | ||||||
chr3:71679528 | A | G | 1 | a0001c0001t0021 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5154T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 5154 | chr3 | 71679528 | ||||||
chr3:71679686 | A | T | 2 | a0001c0001t0029 a0001c0001t0033 |
2 | HG02647.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4996T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4996 | chr3 | 71679686 | ||||||
chr3:71679702 | T | A | 1 | a0001c0001t0061 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4980A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4980 | chr3 | 71679702 | ||||||
chr3:71679860 | C | G | 1 | a0001c0001t0072 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4822G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4822 | chr3 | 71679860 | ||||||
chr3:71679878 | G | A | 1 | a0001c0001t0031 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4804C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4804 | chr3 | 71679878 | ||||||
chr3:71679932 | T | C | 1 | a0001c0001t0008 | 5 | HG02630.hp1 HG02970.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4750A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4750 | chr3 | 71679932 | ||||||
chr3:71679955 | C | T | 8 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0030 others(5): Show |
9 | HG02257.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4727G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4727 | chr3 | 71679955 | ||||||
chr3:71679957 | A | G | 1 | a0001c0001t0023 | 2 | HG02683.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4725T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4725 | chr3 | 71679957 | ||||||
chr3:71680025 | G | A | 1 | a0001c0001t0038 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4657C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4657 | chr3 | 71680025 | ||||||
chr3:71680093 | T | C | 1 | a0001c0001t0014 | 2 | NA18943.hp2 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4589A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4589 | chr3 | 71680093 | ||||||
chr3:71680232 | T | G | 1 | a0001c0001t0039 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4450A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4450 | chr3 | 71680232 | ||||||
chr3:71680261 | G | A | 1 | a0001c0001t0045 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4421C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4421 | chr3 | 71680261 | ||||||
chr3:71680358 | T | C | 1 | a0001c0001t0067 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4324A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4324 | chr3 | 71680358 | ||||||
chr3:71680587 | T | C | 1 | a0001c0001t0077 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4095A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4095 | chr3 | 71680587 | ||||||
chr3:71680643 | C | T | 8 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0030 others(5): Show |
9 | HG02257.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4039G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 4039 | chr3 | 71680643 | ||||||
chr3:71680687 | A | G | 1 | a0001c0001t0017 | 2 | HG02129.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3995T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3995 | chr3 | 71680687 | ||||||
chr3:71680714 | G | A | 8 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0030 others(5): Show |
9 | HG02257.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3968C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3968 | chr3 | 71680714 | ||||||
chr3:71680839 | T | C | 1 | a0001c0001t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3843A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3843 | chr3 | 71680839 | ||||||
chr3:71680951 | G | C | 1 | a0001c0001t0043 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3731C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3731 | chr3 | 71680951 | ||||||
chr3:71681009 | A | T | 1 | a0001c0001t0028 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3673T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3673 | chr3 | 71681009 | ||||||
chr3:71681371 | A | G | 1 | a0001c0001t0050 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3311T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3311 | chr3 | 71681371 | ||||||
chr3:71681390 | G | T | 1 | a0001c0001t0071 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3292C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3292 | chr3 | 71681390 | ||||||
chr3:71681527 | G | A | 1 | a0001c0001t0046 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3155C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3155 | chr3 | 71681527 | ||||||
chr3:71681637 | C | A | 1 | a0001c0001t0031 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3045G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 3045 | chr3 | 71681637 | ||||||
chr3:71681693 | G | A | 1 | a0001c0001t0042 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2989C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2989 | chr3 | 71681693 | ||||||
chr3:71681701 | C | A | 7 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0030 others(4): Show |
8 | HG02257.hp2 HG02451.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2981G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2981 | chr3 | 71681701 | ||||||
chr3:71681714 | C | T | 42 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(39): Show |
166 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*2968G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2968 | chr3 | 71681714 | ||||||
chr3:71681835 | G | T | 1 | a0001c0001t0043 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2847C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2847 | chr3 | 71681835 | ||||||
chr3:71681926 | C | T | 51 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(48): Show |
177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*2756G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2756 | chr3 | 71681926 | ||||||
chr3:71681972 | T | C | 1 | a0001c0001t0078 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2710A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2710 | chr3 | 71681972 | ||||||
chr3:71681977 | C | A | 1 | a0001c0001t0028 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2705G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2705 | chr3 | 71681977 | ||||||
chr3:71681992 | T | A | 8 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0030 others(5): Show |
9 | HG02257.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2690A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2690 | chr3 | 71681992 | ||||||
chr3:71682197 | T | C | 20 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(17): Show |
50 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2485A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2485 | chr3 | 71682197 | ||||||
chr3:71682335 | T | C | 1 | a0001c0001t0068 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2347A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 2347 | chr3 | 71682335 | ||||||
chr3:71682699 | A | T | 1 | a0001c0001t0049 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1983 | chr3 | 71682699 | ||||||
chr3:71682741 | C | T | 1 | a0001c0001t0016 | 2 | HG00733.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1941G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1941 | chr3 | 71682741 | ||||||
chr3:71682890 | C | A | 1 | a0001c0001t0048 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1792G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1792 | chr3 | 71682890 | ||||||
chr3:71682891 | C | G | 1 | a0001c0001t0048 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1791 | chr3 | 71682891 | ||||||
chr3:71683064 | T | G | 1 | a0001c0001t0046 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1618A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1618 | chr3 | 71683064 | ||||||
chr3:71683094 | A | G | 1 | a0001c0001t0008 | 5 | HG02630.hp1 HG02970.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1588T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1588 | chr3 | 71683094 | ||||||
chr3:71683145 | G | A | 1 | a0001c0001t0047 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1537 | chr3 | 71683145 | ||||||
chr3:71683410 | C | T | 1 | a0001c0001t0032 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1272G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1272 | chr3 | 71683410 | ||||||
chr3:71683529 | A | G | 3 | a0001c0001t0029 a0001c0001t0030 a0001c0001t0031 |
3 | HG02647.hp1 HG03516.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1153 | chr3 | 71683529 | ||||||
chr3:71683589 | A | G | 1 | a0001c0001t0028 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1093T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 1093 | chr3 | 71683589 | ||||||
chr3:71683727 | T | G | 1 | a0001c0001t0069 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*955A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 955 | chr3 | 71683727 | ||||||
chr3:71684269 | C | T | 41 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(38): Show |
166 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*413G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 413 | chr3 | 71684269 | ||||||
chr3:71684393 | C | CA | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(44): Show |
218 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*288dupT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 288 | chr3 | 71684393 | ||||||
chr3:71684393 | C | CAA | 8 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0024 others(5): Show |
17 | HG00423.hp2 HG00438.hp1 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*287_*288dupTT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 7/7 | 288 | chr3 | 71684393 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:71684869 | T | A | 1 | a0001c0001t0003g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.629-141A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71684869 | |||||||
chr3:71684988 | G | T | 120 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0039 others(117): Show |
128 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.629-260C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71684988 | |||||||
chr3:71685009 | G | A | 1 | a0001c0001t0045g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.629-281C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685009 | |||||||
chr3:71685015 | G | C | 1 | a0001c0001t0002g0159 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.629-287C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685015 | |||||||
chr3:71685079 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.629-351C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685079 | |||||||
chr3:71685196 | T | C | 1 | a0001c0001t0031g0361 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-468A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685196 | |||||||
chr3:71685370 | A | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG00735.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.629-642T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685370 | |||||||
chr3:71685505 | G | C | 1 | a0001c0001t0052g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.629-777C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685505 | |||||||
chr3:71685523 | A | G | 1 | a0001c0001t0003g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.629-795T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685523 | |||||||
chr3:71685705 | T | TCAAACAC others(47): Show |
1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.629-978_629-977ins others(54): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685705 | |||||||
chr3:71685747 | G | T | 2 | a0001c0001t0015g0100 a0001c0001t0015g0331 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.629-1019C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685747 | |||||||
chr3:71685754 | G | A | 1 | a0001c0001t0001g0364 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.629-1026C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685754 | |||||||
chr3:71685761 | A | G | 2 | a0001c0001t0005g0046 a0001c0001t0026g0091 |
2 | HG00438.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.629-1033T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685761 | |||||||
chr3:71685809 | G | A | 1 | a0001c0001t0005g0269 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.629-1081C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685809 | |||||||
chr3:71685838 | C | T | 2 | a0001c0001t0015g0100 a0001c0001t0015g0331 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.629-1110G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685838 | |||||||
chr3:71685855 | G | A | 2 | a0001c0001t0003g0075 a0001c0001t0003g0076 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.629-1127C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71685855 | |||||||
chr3:71686064 | C | A | 2 | a0001c0001t0029g0104 a0001c0001t0030g0020 |
2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.629-1336G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686064 | |||||||
chr3:71686236 | G | C | 171 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0039 others(168): Show |
179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.629-1508C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686236 | |||||||
chr3:71686253 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.629-1525C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686253 | |||||||
chr3:71686448 | C | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
92 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.629-1720G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686448 | |||||||
chr3:71686502 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0258 a0001c0001t0001g0318 |
3 | HG01123.hp2 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.629-1774T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686502 | |||||||
chr3:71686543 | A | AGT | 100 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0231 others(97): Show |
110 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.629-1817_629-1816d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGT | 75 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0066 others(72): Show |
77 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.629-1819_629-1816d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGT | 8 | a0001c0001t0001g0042 a0001c0001t0003g0152 a0001c0001t0003g0271 others(5): Show |
8 | HG00621.hp2 HG02040.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.629-1821_629-1816d others(8): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0308 a0001c0001t0002g0178 a0001c0001t0005g0110 others(4): Show |
7 | HG02451.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.629-1823_629-1816d others(10): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGTG others(3): Show |
4 | a0001c0001t0005g0046 a0001c0001t0005g0230 a0001c0001t0005g0337 others(1): Show |
4 | HG00438.hp1 HG02602.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-1825_629-1816d others(12): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGTG others(5): Show |
5 | a0001c0001t0005g0206 a0001c0001t0005g0245 a0001c0001t0021g0224 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-1827_629-1816d others(14): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGTG others(7): Show |
5 | a0001c0001t0005g0269 a0001c0001t0010g0165 a0001c0001t0016g0108 others(2): Show |
5 | HG00733.hp1 HG02027.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-1829_629-1816d others(16): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGTG others(9): Show |
5 | a0001c0001t0005g0268 a0001c0001t0005g0301 a0001c0001t0010g0170 others(2): Show |
5 | HG00280.hp1 HG02056.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-1831_629-1816d others(18): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGTG others(11): Show |
3 | a0001c0001t0005g0148 a0001c0001t0062g0167 a0001c0001t0063g0265 |
3 | HG01975.hp1 HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.629-1833_629-1816d others(20): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | A | AGTGTGTG others(13): Show |
1 | a0001c0001t0005g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.629-1835_629-1816d others(22): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | AGT | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0092 others(17): Show |
20 | HG00735.hp1 HG01243.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.629-1817_629-1816d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | AGTGT | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(34): Show |
42 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.629-1819_629-1816d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686543 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0003g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.629-1827_629-1816d others(14): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686543 | |||||||
chr3:71686579 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0079g0338 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.629-1852_629-1851i others(17): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686579 | |||||||
chr3:71686580 | T | G | 1 | a0001c0001t0001g0282 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.629-1852A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686580 | |||||||
chr3:71686613 | C | A | 6 | a0001c0001t0001g0231 a0001c0001t0003g0233 a0001c0001t0029g0104 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-1885G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686613 | |||||||
chr3:71686712 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0001g0275 |
3 | HG00544.hp2 HG02040.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.629-1984A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686712 | |||||||
chr3:71686747 | T | G | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.629-2019A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71686747 | |||||||
chr3:71687021 | A | T | 60 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(57): Show |
63 | HG00621.hp2 HG00642.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.629-2293T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687021 | |||||||
chr3:71687022 | CAG | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0297 a0001c0001t0035g0343 |
3 | HG01243.hp2 HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.629-2296_629-2295d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687022 | |||||||
chr3:71687030 | T | C | 50 | a0001c0001t0005g0046 a0001c0001t0005g0110 a0001c0001t0005g0148 others(47): Show |
50 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.629-2302A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687030 | |||||||
chr3:71687130 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.629-2402T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687130 | |||||||
chr3:71687327 | T | C | 2 | a0001c0001t0001g0368 a0001c0001t0001g0369 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.629-2599A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687327 | |||||||
chr3:71687356 | C | T | 1 | a0001c0001t0028g0022 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.629-2628G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687356 | |||||||
chr3:71687357 | G | A | 1 | a0001c0001t0045g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.629-2629C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687357 | |||||||
chr3:71687396 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.628+2614A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687396 | |||||||
chr3:71687584 | A | G | 371 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(368): Show |
395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.628+2426T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687584 | |||||||
chr3:71687615 | T | G | 1 | a0001c0001t0007g0367 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.628+2395A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687615 | |||||||
chr3:71687690 | A | G | 1 | a0001c0001t0043g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628+2320T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687690 | |||||||
chr3:71687745 | C | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0190 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+2265G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687745 | |||||||
chr3:71687866 | C | G | 1 | a0001c0001t0071g0216 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.628+2144G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687866 | |||||||
chr3:71687868 | T | C | 5 | a0001c0001t0015g0100 a0001c0001t0015g0331 a0001c0001t0028g0022 others(2): Show |
5 | HG02451.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+2142A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687868 | |||||||
chr3:71687956 | A | G | 172 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0039 others(169): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.628+2054T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71687956 | |||||||
chr3:71688015 | G | GT | 177 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0190 others(174): Show |
185 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.628+1994dupA | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71688015 | |||||||
chr3:71688804 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.628+1206A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71688804 | |||||||
chr3:71688863 | A | C | 1 | a0001c0001t0003g0034 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.628+1147T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71688863 | |||||||
chr3:71688975 | T | C | 1 | a0001c0001t0046g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.628+1035A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71688975 | |||||||
chr3:71689070 | G | A | 1 | a0001c0001t0044g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.628+940C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689070 | |||||||
chr3:71689275 | T | G | 1 | a0001c0001t0043g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628+735A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689275 | |||||||
chr3:71689570 | C | T | 1 | a0001c0001t0039g0307 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.628+440G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689570 | |||||||
chr3:71689654 | T | C | 5 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0208 others(2): Show |
5 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+356A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689654 | |||||||
chr3:71689801 | G | T | 1 | a0001c0001t0028g0022 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.628+209C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689801 | |||||||
chr3:71689846 | G | GT | 12 | a0001c0001t0002g0164 a0001c0001t0002g0178 a0001c0001t0002g0286 others(9): Show |
12 | HG00609.hp2 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.628+163dupA | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689846 | |||||||
chr3:71689854 | T | A | 2 | a0001c0001t0001g0319 a0001c0001t0003g0075 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.628+156A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689854 | |||||||
chr3:71689854 | TA | T | 10 | a0001c0001t0001g0042 a0001c0001t0001g0129 a0001c0001t0001g0259 others(7): Show |
10 | HG01070.hp1 HG01256.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.628+155delT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689854 | |||||||
chr3:71689855 | A | T | 38 | a0001c0001t0001g0339 a0001c0001t0005g0046 a0001c0001t0005g0110 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.628+155T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689855 | |||||||
chr3:71689856 | A | T | 1 | a0001c0001t0046g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.628+154T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689856 | |||||||
chr3:71689867 | A | AC | 113 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0039 others(110): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.628+142_628+143ins others(1): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689867 | |||||||
chr3:71689867 | A | C | 55 | a0001c0001t0002g0164 a0001c0001t0002g0178 a0001c0001t0002g0238 others(52): Show |
55 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.628+143T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689867 | |||||||
chr3:71689887 | A | T | 42 | a0001c0001t0005g0046 a0001c0001t0005g0110 a0001c0001t0005g0148 others(39): Show |
42 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.628+123T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689887 | |||||||
chr3:71689919 | A | G | 169 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0039 others(166): Show |
177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.628+91T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689919 | |||||||
chr3:71689965 | T | C | 1 | a0001c0001t0002g0183 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.628+45A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 6/6 | chr3 | 71689965 | |||||||
chr3:71690181 | G | GA | 9 | a0001c0001t0003g0006 a0001c0001t0003g0018 a0001c0001t0003g0070 others(6): Show |
10 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.473-17dupT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690181 | |||||||
chr3:71690413 | A | C | 45 | a0001c0001t0005g0046 a0001c0001t0005g0110 a0001c0001t0005g0148 others(42): Show |
45 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.473-248T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690413 | |||||||
chr3:71690423 | T | G | 1 | a0001c0001t0001g0275 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.473-258A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690423 | |||||||
chr3:71690453 | A | G | 1 | a0001c0001t0046g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.473-288T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690453 | |||||||
chr3:71690518 | T | C | 1 | a0001c0001t0004g0181 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.473-353A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690518 | |||||||
chr3:71690797 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.473-632C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690797 | |||||||
chr3:71690861 | G | C | 2 | a0001c0001t0015g0100 a0001c0001t0015g0331 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.473-696C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690861 | |||||||
chr3:71690902 | C | T | 2 | a0001c0001t0015g0100 a0001c0001t0015g0331 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.473-737G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690902 | |||||||
chr3:71690959 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.473-794T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71690959 | |||||||
chr3:71691060 | A | G | 1 | a0001c0001t0043g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.473-895T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691060 | |||||||
chr3:71691285 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0293 |
3 | HG01074.hp1 HG03927.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.473-1120A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691285 | |||||||
chr3:71691401 | T | C | 110 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0039 others(107): Show |
118 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.473-1236A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691401 | |||||||
chr3:71691508 | C | T | 65 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(62): Show |
68 | HG00621.hp2 HG00642.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.473-1343G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691508 | |||||||
chr3:71691523 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.473-1358A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691523 | |||||||
chr3:71691560 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.473-1395C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691560 | |||||||
chr3:71691589 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.473-1424G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691589 | |||||||
chr3:71691675 | C | T | 65 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(62): Show |
68 | HG00621.hp2 HG00642.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.473-1510G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691675 | |||||||
chr3:71691705 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.473-1540G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691705 | |||||||
chr3:71691917 | T | C | 66 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(63): Show |
69 | HG00621.hp2 HG00642.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.473-1752A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71691917 | |||||||
chr3:71692007 | A | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.473-1842T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692007 | |||||||
chr3:71692017 | T | C | 1 | a0001c0001t0043g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.473-1852A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692017 | |||||||
chr3:71692031 | T | A | 2 | a0001c0001t0001g0139 a0001c0001t0003g0083 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.472+1844A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692031 | |||||||
chr3:71692098 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.472+1777C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692098 | |||||||
chr3:71692103 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.472+1772C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692103 | |||||||
chr3:71692187 | C | G | 30 | a0001c0001t0004g0001 a0001c0001t0004g0010 a0001c0001t0004g0012 others(27): Show |
38 | HG00639.hp1 HG01071.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.472+1688G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692187 | |||||||
chr3:71692341 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.472+1534G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692341 | |||||||
chr3:71692406 | C | A | 113 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0039 others(110): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.472+1469G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692406 | |||||||
chr3:71692426 | G | C | 1 | a0001c0001t0002g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.472+1449C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692426 | |||||||
chr3:71692539 | T | G | 1 | a0001c0001t0031g0361 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.472+1336A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692539 | |||||||
chr3:71692593 | GTCT | G | 3 | a0001c0001t0003g0048 a0001c0001t0003g0203 a0001c0001t0004g0373 |
3 | HG04184.hp2 NA18943.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.472+1279_472+1281d others(5): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692593 | |||||||
chr3:71692596 | TTC | T | 172 | a0001c0001t0001g0231 a0001c0001t0002g0033 a0001c0001t0002g0037 others(169): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.472+1277_472+1278d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692596 | |||||||
chr3:71692597 | TC | T | 6 | a0001c0001t0003g0070 a0001c0001t0015g0100 a0001c0001t0015g0331 others(3): Show |
6 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+1277delG | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692597 | |||||||
chr3:71692598 | C | T | 1 | a0001c0001t0031g0361 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.472+1277G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692598 | |||||||
chr3:71692619 | A | T | 1 | a0002c0002t0007g0173 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.472+1256T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692619 | |||||||
chr3:71692847 | G | A | 1 | a0001c0001t0031g0361 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.472+1028C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692847 | |||||||
chr3:71692976 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.472+899C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692976 | |||||||
chr3:71692988 | T | C | 111 | a0001c0001t0001g0282 a0001c0001t0002g0033 a0001c0001t0002g0037 others(108): Show |
119 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.472+887A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71692988 | |||||||
chr3:71693340 | A | T | 1 | a0001c0001t0015g0100 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.472+535T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71693340 | |||||||
chr3:71693423 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.472+452C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71693423 | |||||||
chr3:71693504 | G | C | 1 | a0001c0001t0069g0093 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.472+371C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71693504 | |||||||
chr3:71693632 | A | T | 2 | a0001c0001t0006g0304 a0001c0001t0006g0305 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.472+243T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71693632 | |||||||
chr3:71693715 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.472+160G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71693715 | |||||||
chr3:71693839 | C | T | 1 | a0001c0001t0071g0216 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.472+36G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71693839 | |||||||
chr3:71693850 | C | T | 4 | a0001c0001t0005g0268 a0001c0001t0005g0269 a0001c0001t0026g0255 others(1): Show |
4 | NA18953.hp2 NA19066.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+25G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 5/6 | chr3 | 71693850 | |||||||
chr3:71693961 | A | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | HG01167.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.406-20T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71693961 | |||||||
chr3:71694106 | T | C | 1 | a0001c0001t0029g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.406-165A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694106 | |||||||
chr3:71694530 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.406-589A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694530 | |||||||
chr3:71694532 | C | T | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.406-591G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694532 | |||||||
chr3:71694557 | T | TCAGTC | 109 | a0001c0001t0001g0355 a0001c0001t0002g0033 a0001c0001t0002g0037 others(106): Show |
117 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.406-617_406-616ins others(5): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694557 | |||||||
chr3:71694589 | G | C | 1 | a0001c0001t0056g0283 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.406-648C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694589 | |||||||
chr3:71694655 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(116): Show |
124 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.406-714T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694655 | |||||||
chr3:71694672 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.406-731A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694672 | |||||||
chr3:71694728 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.406-787C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694728 | |||||||
chr3:71694948 | T | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0088 a0001c0001t0001g0089 others(17): Show |
21 | HG01255.hp2 HG02451.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.406-1007A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694948 | |||||||
chr3:71694967 | T | C | 1 | a0001c0001t0034g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.406-1026A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694967 | |||||||
chr3:71694973 | G | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0107 others(2): Show |
8 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.406-1032C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71694973 | |||||||
chr3:71695260 | A | G | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+1200T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695260 | |||||||
chr3:71695321 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.405+1139C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695321 | |||||||
chr3:71695325 | A | G | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+1135T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695325 | |||||||
chr3:71695344 | T | A | 39 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0139 others(36): Show |
40 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.405+1116A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695344 | |||||||
chr3:71695436 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.405+1024A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695436 | |||||||
chr3:71695500 | T | C | 34 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(31): Show |
35 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.405+960A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695500 | |||||||
chr3:71695528 | C | T | 4 | a0001c0001t0001g0297 a0001c0001t0003g0210 a0001c0001t0046g0205 others(1): Show |
4 | HG02523.hp1 HG03239.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+932G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695528 | |||||||
chr3:71695533 | A | G | 1 | a0001c0001t0068g0309 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.405+927T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695533 | |||||||
chr3:71695628 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.405+832G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695628 | |||||||
chr3:71695650 | G | A | 77 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(74): Show |
78 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.405+810C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695650 | |||||||
chr3:71695861 | A | G | 15 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0201 others(12): Show |
15 | HG01361.hp1 HG01952.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.405+599T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695861 | |||||||
chr3:71695962 | G | A | 1 | a0001c0001t0003g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.405+498C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71695962 | |||||||
chr3:71696013 | G | A | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0317 others(1): Show |
4 | HG02717.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+447C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696013 | |||||||
chr3:71696069 | TC | T | 3 | a0001c0001t0001g0009 a0001c0001t0003g0242 a0001c0001t0005g0301 |
4 | HG00280.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+390delG | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696069 | |||||||
chr3:71696219 | C | T | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.405+241G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696219 | |||||||
chr3:71696229 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0051g0040 |
2 | NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.405+231G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696229 | |||||||
chr3:71696249 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(171): Show |
182 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.405+211G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696249 | |||||||
chr3:71696258 | G | A | 2 | a0001c0001t0003g0084 a0001c0001t0022g0085 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.405+202C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696258 | |||||||
chr3:71696426 | C | T | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00741.hp2 HG01346.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.405+34G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696426 | |||||||
chr3:71696430 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.405+30C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 4/6 | chr3 | 71696430 | |||||||
chr3:71696537 | C | T | 23 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0115 others(20): Show |
23 | HG01361.hp1 HG01891.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.345-17G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696537 | |||||||
chr3:71696599 | A | G | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.345-79T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696599 | |||||||
chr3:71696600 | C | T | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.345-80G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696600 | |||||||
chr3:71696661 | T | A | 23 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0115 others(20): Show |
23 | HG01361.hp1 HG01891.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.345-141A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696661 | |||||||
chr3:71696719 | A | AT | 12 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0191 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-200dupA | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696719 | |||||||
chr3:71696719 | A | ATT | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0062 others(55): Show |
59 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.345-201_345-200dup others(2): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696719 | |||||||
chr3:71696719 | A | ATTT | 21 | a0001c0001t0001g0021 a0001c0001t0001g0139 a0001c0001t0001g0140 others(18): Show |
21 | HG00741.hp2 HG01346.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.345-202_345-200dup others(3): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696719 | |||||||
chr3:71696743 | G | T | 79 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(76): Show |
80 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.345-223C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696743 | |||||||
chr3:71696801 | T | G | 2 | a0001c0001t0003g0362 a0001c0001t0031g0361 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.345-281A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696801 | |||||||
chr3:71696860 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.345-340G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696860 | |||||||
chr3:71696884 | T | A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0201 others(13): Show |
16 | HG01361.hp1 HG01952.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-364A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696884 | |||||||
chr3:71696954 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0274 others(26): Show |
31 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-434C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696954 | |||||||
chr3:71696988 | G | A | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345-468C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71696988 | |||||||
chr3:71697014 | G | A | 1 | a0001c0001t0047g0067 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.345-494C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697014 | |||||||
chr3:71697068 | T | C | 81 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(78): Show |
82 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.345-548A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697068 | |||||||
chr3:71697089 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.345-569G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697089 | |||||||
chr3:71697127 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0074 a0001c0001t0002g0052 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-607C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697127 | |||||||
chr3:71697187 | T | A | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345-667A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697187 | |||||||
chr3:71697235 | C | T | 1 | a0001c0001t0043g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.345-715G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697235 | |||||||
chr3:71697258 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.345-738G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697258 | |||||||
chr3:71697296 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0017g0073 |
2 | HG00609.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.345-776G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697296 | |||||||
chr3:71697445 | T | A | 1 | a0001c0001t0001g0363 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.345-925A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697445 | |||||||
chr3:71697571 | T | C | 15 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00741.hp2 HG01346.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-1051A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697571 | |||||||
chr3:71697589 | G | A | 2 | a0001c0001t0002g0159 a0002c0002t0007g0173 |
2 | NA18962.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.345-1069C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697589 | |||||||
chr3:71697894 | C | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(24): Show |
27 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.345-1374G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71697894 | |||||||
chr3:71698057 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0312 |
2 | HG00673.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.345-1537G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698057 | |||||||
chr3:71698076 | A | T | 15 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00741.hp2 HG01346.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.344+1538T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698076 | |||||||
chr3:71698137 | T | C | 1 | a0001c0001t0004g0012 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.344+1477A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698137 | |||||||
chr3:71698223 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.344+1391C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698223 | |||||||
chr3:71698252 | A | T | 15 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00741.hp2 HG01346.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.344+1362T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698252 | |||||||
chr3:71698280 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(159): Show |
170 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.344+1334G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698280 | |||||||
chr3:71698325 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.344+1289A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698325 | |||||||
chr3:71698412 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.344+1202C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698412 | |||||||
chr3:71698519 | C | T | 24 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0115 others(21): Show |
24 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.344+1095G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698519 | |||||||
chr3:71698560 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.344+1054G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698560 | |||||||
chr3:71698561 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.344+1053C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698561 | |||||||
chr3:71698678 | A | T | 73 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0062 others(70): Show |
74 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.344+936T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698678 | |||||||
chr3:71698680 | A | C | 73 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0062 others(70): Show |
74 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.344+934T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698680 | |||||||
chr3:71698766 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(83): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.344+848G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698766 | |||||||
chr3:71698824 | C | T | 71 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0062 others(68): Show |
72 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.344+790G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698824 | |||||||
chr3:71698922 | C | T | 71 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0062 others(68): Show |
72 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.344+692G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698922 | |||||||
chr3:71698926 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.344+688A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698926 | |||||||
chr3:71698929 | C | T | 3 | a0001c0001t0002g0183 a0001c0001t0002g0185 a0001c0001t0002g0253 |
3 | HG02056.hp2 NA18950.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.344+685G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698929 | |||||||
chr3:71698930 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(89): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.344+684T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71698930 | |||||||
chr3:71699058 | C | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(162): Show |
172 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.344+556G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699058 | |||||||
chr3:71699076 | A | G | 2 | a0001c0001t0003g0362 a0001c0001t0031g0361 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.344+538T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699076 | |||||||
chr3:71699077 | A | G | 1 | a0001c0001t0043g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.344+537T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699077 | |||||||
chr3:71699124 | G | T | 2 | a0001c0001t0003g0362 a0001c0001t0031g0361 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.344+490C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699124 | |||||||
chr3:71699176 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.344+438C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699176 | |||||||
chr3:71699260 | C | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0033g0193 |
3 | HG02895.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.344+354G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699260 | |||||||
chr3:71699268 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0005g0230 a0001c0001t0021g0224 others(2): Show |
6 | HG00738.hp1 HG00738.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+346T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699268 | |||||||
chr3:71699269 | C | A | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+345G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699269 | |||||||
chr3:71699303 | T | C | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.344+311A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699303 | |||||||
chr3:71699339 | T | C | 1 | a0001c0001t0004g0143 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.344+275A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699339 | |||||||
chr3:71699474 | C | A | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+140G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699474 | |||||||
chr3:71699475 | C | T | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+139G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699475 | |||||||
chr3:71699476 | A | G | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+138T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699476 | |||||||
chr3:71699489 | T | C | 1 | a0001c0001t0003g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.344+125A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699489 | |||||||
chr3:71699492 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(91): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.344+122A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699492 | |||||||
chr3:71699503 | G | C | 30 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0204 others(27): Show |
31 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.344+111C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699503 | |||||||
chr3:71699600 | C | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(31): Show |
35 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.344+14G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 3/6 | chr3 | 71699600 | |||||||
chr3:71699727 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.250-19G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71699727 | |||||||
chr3:71699760 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(91): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.250-52T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71699760 | |||||||
chr3:71699988 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(87): Show |
97 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.250-280A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71699988 | |||||||
chr3:71700107 | G | A | 1 | a0001c0001t0013g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.250-399C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700107 | |||||||
chr3:71700130 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0003g0018 a0001c0001t0003g0070 others(5): Show |
8 | HG02486.hp2 HG02723.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-422C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700130 | |||||||
chr3:71700140 | A | T | 2 | a0001c0001t0003g0362 a0001c0001t0031g0361 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.250-432T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700140 | |||||||
chr3:71700166 | C | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(156): Show |
166 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.250-458G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700166 | |||||||
chr3:71700173 | C | T | 1 | a0001c0001t0077g0182 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.250-465G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700173 | |||||||
chr3:71700242 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.250-534A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700242 | |||||||
chr3:71700302 | A | T | 2 | a0001c0001t0002g0081 a0001c0001t0061g0080 |
2 | NA19074.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.250-594T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700302 | |||||||
chr3:71700545 | C | T | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.250-837G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700545 | |||||||
chr3:71700554 | C | A | 24 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0115 others(21): Show |
24 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.250-846G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700554 | |||||||
chr3:71700609 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250-901C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700609 | |||||||
chr3:71700612 | T | TA | 127 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(124): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.250-905dupT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700612 | |||||||
chr3:71700612 | T | TAA | 40 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0062 others(37): Show |
41 | HG00738.hp1 HG00738.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.250-906_250-905dup others(2): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700612 | |||||||
chr3:71700612 | TA | T | 27 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0139 others(24): Show |
28 | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.250-905delT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700612 | |||||||
chr3:71700612 | TAA | T | 19 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0201 others(16): Show |
19 | HG01175.hp2 HG01346.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-906_250-905del others(2): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700612 | |||||||
chr3:71700639 | C | A | 3 | a0001c0001t0001g0021 a0001c0001t0030g0020 a0001c0001t0032g0019 |
3 | HG02257.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.250-931G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700639 | |||||||
chr3:71700693 | T | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(157): Show |
167 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.250-985A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700693 | |||||||
chr3:71700821 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0314 a0001c0001t0001g0315 |
4 | NA18971.hp2 NA19056.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-1113G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700821 | |||||||
chr3:71700992 | A | G | 47 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(44): Show |
48 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.250-1284T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71700992 | |||||||
chr3:71701029 | G | A | 99 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(96): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.250-1321C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701029 | |||||||
chr3:71701219 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.250-1511A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701219 | |||||||
chr3:71701325 | C | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(165): Show |
176 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.250-1617G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701325 | |||||||
chr3:71701355 | T | G | 49 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(46): Show |
50 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.250-1647A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701355 | |||||||
chr3:71701397 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.250-1689C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701397 | |||||||
chr3:71701510 | C | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(172): Show |
183 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.250-1802G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701510 | |||||||
chr3:71701577 | G | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0017 others(119): Show |
128 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.250-1869C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701577 | |||||||
chr3:71701895 | T | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(266): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.250-2187A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701895 | |||||||
chr3:71701914 | C | T | 1 | a0001c0001t0070g0130 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.250-2206G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71701914 | |||||||
chr3:71702021 | G | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.250-2313C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702021 | |||||||
chr3:71702039 | G | T | 1 | a0001c0001t0001g0336 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.250-2331C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702039 | |||||||
chr3:71702142 | AAT | A | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00741.hp2 HG01346.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.250-2436_250-2435d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702142 | |||||||
chr3:71702364 | G | C | 2 | a0001c0001t0022g0197 a0001c0001t0064g0196 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.250-2656C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702364 | |||||||
chr3:71702365 | T | C | 1 | a0001c0001t0003g0362 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.250-2657A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702365 | |||||||
chr3:71702523 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250-2815T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702523 | |||||||
chr3:71702527 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0365 |
2 | NA18970.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.250-2819A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702527 | |||||||
chr3:71702699 | C | T | 1 | a0001c0001t0023g0296 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.250-2991G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702699 | |||||||
chr3:71702711 | T | TA | 70 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0062 others(67): Show |
71 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.250-3004dupT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702711 | |||||||
chr3:71702711 | T | TAA | 8 | a0001c0001t0003g0029 a0001c0001t0003g0126 a0001c0001t0006g0122 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-3005_250-3004d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702711 | |||||||
chr3:71702711 | TA | T | 9 | a0001c0001t0001g0044 a0001c0001t0001g0315 a0001c0001t0001g0329 others(6): Show |
9 | HG01243.hp2 HG01975.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-3004delT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702711 | |||||||
chr3:71702815 | C | G | 5 | a0001c0001t0001g0016 a0001c0001t0005g0230 a0001c0001t0021g0224 others(2): Show |
6 | HG00738.hp1 HG00738.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-3107G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702815 | |||||||
chr3:71702926 | A | T | 1 | a0001c0001t0001g0297 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.250-3218T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71702926 | |||||||
chr3:71703110 | T | C | 1 | a0001c0001t0002g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.250-3402A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703110 | |||||||
chr3:71703196 | T | C | 2 | a0001c0001t0006g0302 a0001c0001t0044g0207 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.250-3488A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703196 | |||||||
chr3:71703199 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.250-3491A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703199 | |||||||
chr3:71703248 | G | A | 4 | a0001c0001t0001g0297 a0001c0001t0003g0210 a0001c0001t0046g0205 others(1): Show |
4 | HG02523.hp1 HG03239.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-3540C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703248 | |||||||
chr3:71703256 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(162): Show |
173 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.250-3548A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703256 | |||||||
chr3:71703601 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(162): Show |
173 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.250-3893G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703601 | |||||||
chr3:71703683 | T | A | 6 | a0001c0001t0001g0332 a0001c0001t0001g0355 a0001c0001t0001g0357 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-3975A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703683 | |||||||
chr3:71703712 | A | G | 15 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00741.hp2 HG01346.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.250-4004T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703712 | |||||||
chr3:71703811 | C | CA | 86 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(83): Show |
90 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.250-4104dupT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703811 | |||||||
chr3:71703811 | C | CAA | 19 | a0001c0001t0001g0074 a0001c0001t0001g0086 a0001c0001t0001g0115 others(16): Show |
19 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.250-4105_250-4104d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703811 | |||||||
chr3:71703811 | C | CAAA | 13 | a0001c0001t0001g0116 a0001c0001t0001g0140 a0001c0001t0001g0141 others(10): Show |
13 | HG02258.hp2 HG02300.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-4106_250-4104d others(5): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703811 | |||||||
chr3:71703811 | C | CAAAA | 17 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(14): Show |
17 | HG01175.hp2 HG01346.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-4107_250-4104d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703811 | |||||||
chr3:71703811 | CA | C | 20 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0314 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.250-4104delT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703811 | |||||||
chr3:71703811 | CAAAAA | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(28): Show |
32 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.250-4108_250-4104d others(7): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703811 | |||||||
chr3:71703955 | A | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(167): Show |
177 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.250-4247T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703955 | |||||||
chr3:71703967 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.250-4259A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71703967 | |||||||
chr3:71704047 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(159): Show |
169 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.250-4339C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704047 | |||||||
chr3:71704079 | G | A | 1 | a0001c0001t0010g0165 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250-4371C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704079 | |||||||
chr3:71704259 | T | C | 7 | a0001c0001t0003g0126 a0001c0001t0003g0330 a0001c0001t0006g0122 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-4551A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704259 | |||||||
chr3:71704279 | G | C | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.250-4571C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704279 | |||||||
chr3:71704295 | G | C | 2 | a0001c0001t0001g0356 a0001c0001t0001g0359 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.250-4587C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704295 | |||||||
chr3:71704387 | T | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0014 |
5 | HG00642.hp1 HG00741.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-4679A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704387 | |||||||
chr3:71704415 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.250-4707C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704415 | |||||||
chr3:71704430 | G | A | 15 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00741.hp2 HG01346.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.250-4722C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704430 | |||||||
chr3:71704448 | C | T | 1 | a0001c0001t0003g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.250-4740G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704448 | |||||||
chr3:71704591 | G | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(93): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.250-4883C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704591 | |||||||
chr3:71704798 | T | C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(18): Show |
21 | HG01361.hp1 HG01952.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-5090A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704798 | |||||||
chr3:71704835 | G | A | 274 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(271): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.250-5127C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704835 | |||||||
chr3:71704905 | T | C | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.250-5197A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704905 | |||||||
chr3:71704922 | A | C | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.250-5214T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71704922 | |||||||
chr3:71705032 | C | A | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-5324G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705032 | |||||||
chr3:71705079 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0030g0020 a0001c0001t0032g0019 |
3 | HG02257.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.249+5333A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705079 | |||||||
chr3:71705218 | C | T | 30 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(27): Show |
30 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.249+5194G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705218 | |||||||
chr3:71705319 | T | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG00735.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.249+5093A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705319 | |||||||
chr3:71705338 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.249+5074C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705338 | |||||||
chr3:71705446 | T | C | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4966A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705446 | |||||||
chr3:71705492 | T | C | 1 | a0001c0001t0001g0357 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.249+4920A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705492 | |||||||
chr3:71705501 | T | C | 30 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(27): Show |
30 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.249+4911A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705501 | |||||||
chr3:71705528 | A | G | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+4884T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705528 | |||||||
chr3:71705609 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(83): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.249+4803G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705609 | |||||||
chr3:71705626 | G | A | 2 | a0001c0001t0003g0006 a0001c0001t0074g0328 |
3 | NA19043.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.249+4786C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705626 | |||||||
chr3:71705656 | C | T | 5 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+4756G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705656 | |||||||
chr3:71705805 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.249+4607G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71705805 | |||||||
chr3:71706045 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.249+4367G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706045 | |||||||
chr3:71706096 | A | G | 1 | a0001c0001t0001g0364 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.249+4316T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706096 | |||||||
chr3:71706205 | G | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(30): Show |
34 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.249+4207C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706205 | |||||||
chr3:71706241 | G | C | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4171C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706241 | |||||||
chr3:71706253 | A | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(83): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.249+4159T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706253 | |||||||
chr3:71706261 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(83): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.249+4151G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706261 | |||||||
chr3:71706337 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(82): Show |
91 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+4075C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706337 | |||||||
chr3:71706526 | G | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.249+3886C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706526 | |||||||
chr3:71706671 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.249+3741A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706671 | |||||||
chr3:71706739 | C | A | 3 | a0001c0001t0001g0103 a0001c0001t0008g0102 a0001c0001t0029g0104 |
3 | HG02647.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.249+3673G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706739 | |||||||
chr3:71706777 | A | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.249+3635T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706777 | |||||||
chr3:71706864 | A | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(264): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.249+3548T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706864 | |||||||
chr3:71706887 | T | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(82): Show |
91 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+3525A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706887 | |||||||
chr3:71706964 | C | T | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+3448G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71706964 | |||||||
chr3:71707021 | T | A | 1 | a0001c0001t0059g0284 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.249+3391A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707021 | |||||||
chr3:71707038 | T | A | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+3374A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707038 | |||||||
chr3:71707121 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0027 others(70): Show |
75 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.249+3291C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707121 | |||||||
chr3:71707193 | T | C | 2 | a0001c0001t0006g0302 a0001c0001t0044g0207 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.249+3219A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707193 | |||||||
chr3:71707224 | A | C | 109 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(106): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.249+3188T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707224 | |||||||
chr3:71707235 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.249+3177T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707235 | |||||||
chr3:71707246 | C | T | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+3166G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707246 | |||||||
chr3:71707356 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.249+3056G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707356 | |||||||
chr3:71707393 | C | A | 1 | a0001c0001t0005g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.249+3019G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707393 | |||||||
chr3:71707470 | T | A | 1 | a0001c0001t0035g0343 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.249+2942A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707470 | |||||||
chr3:71707598 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.249+2814G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707598 | |||||||
chr3:71707610 | T | C | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.249+2802A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707610 | |||||||
chr3:71707614 | C | T | 74 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0086 others(71): Show |
77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.249+2798G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707614 | |||||||
chr3:71707772 | A | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.249+2640T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707772 | |||||||
chr3:71707871 | C | CT | 46 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0001t0001g0204 others(43): Show |
47 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.249+2540dupA | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707871 | |||||||
chr3:71707871 | C | CTT | 33 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0066 others(30): Show |
34 | HG01074.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.249+2539_249+2540d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707871 | |||||||
chr3:71707871 | CT | C | 8 | a0001c0001t0001g0359 a0001c0001t0002g0288 a0001c0001t0002g0360 others(5): Show |
8 | HG01516.hp2 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+2540delA | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707871 | |||||||
chr3:71707876 | T | C | 1 | a0001c0001t0062g0167 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.249+2536A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71707876 | |||||||
chr3:71708084 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.249+2328C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708084 | |||||||
chr3:71708102 | G | C | 4 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0039g0307 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+2310C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708102 | |||||||
chr3:71708109 | A | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): Show |
162 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.249+2303T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708109 | |||||||
chr3:71708124 | T | G | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.249+2288A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708124 | |||||||
chr3:71708141 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249+2271C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708141 | |||||||
chr3:71708183 | C | T | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+2229G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708183 | |||||||
chr3:71708266 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(152): Show |
163 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.249+2146C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708266 | |||||||
chr3:71708296 | G | T | 1 | a0001c0001t0049g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.249+2116C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708296 | |||||||
chr3:71708385 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.249+2027C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708385 | |||||||
chr3:71708389 | T | C | 106 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(103): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.249+2023A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708389 | |||||||
chr3:71708436 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): Show |
162 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.249+1976G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708436 | |||||||
chr3:71708487 | T | C | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.249+1925A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708487 | |||||||
chr3:71708499 | G | A | 1 | a0001c0001t0062g0167 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.249+1913C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708499 | |||||||
chr3:71708561 | T | C | 1 | a0001c0001t0003g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.249+1851A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708561 | |||||||
chr3:71708581 | CT | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.249+1830delA | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708581 | |||||||
chr3:71708585 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249+1827A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708585 | |||||||
chr3:71708719 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0002g0262 |
3 | HG00544.hp2 HG02040.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.249+1693G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708719 | |||||||
chr3:71708740 | C | T | 1 | a0001c0001t0043g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.249+1672G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708740 | |||||||
chr3:71708744 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.249+1668C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708744 | |||||||
chr3:71708760 | G | A | 2 | a0001c0001t0003g0362 a0001c0001t0031g0361 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.249+1652C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708760 | |||||||
chr3:71708864 | A | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.249+1548T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708864 | |||||||
chr3:71708938 | C | T | 1 | a0001c0001t0004g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.249+1474G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71708938 | |||||||
chr3:71709025 | A | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): Show |
162 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.249+1387T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709025 | |||||||
chr3:71709046 | T | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0201 others(13): Show |
16 | HG01361.hp1 HG01952.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.249+1366A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709046 | |||||||
chr3:71709073 | C | A | 1 | a0001c0001t0002g0081 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.249+1339G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709073 | |||||||
chr3:71709113 | C | G | 8 | a0001c0001t0003g0126 a0001c0001t0003g0330 a0001c0001t0006g0122 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+1299G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709113 | |||||||
chr3:71709442 | T | C | 30 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(27): Show |
30 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.249+970A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709442 | |||||||
chr3:71709672 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(154): Show |
166 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.249+740G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709672 | |||||||
chr3:71709677 | G | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(30): Show |
34 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.249+735C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709677 | |||||||
chr3:71709719 | T | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(28): Show |
32 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.249+693A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709719 | |||||||
chr3:71709855 | G | A | 4 | a0001c0001t0002g0183 a0001c0001t0002g0185 a0001c0001t0002g0253 others(1): Show |
4 | HG02056.hp2 NA18950.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+557C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709855 | |||||||
chr3:71709858 | AC | A | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+553delG | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709858 | |||||||
chr3:71709924 | C | T | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+488G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709924 | |||||||
chr3:71709991 | T | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(30): Show |
34 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.249+421A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71709991 | |||||||
chr3:71710029 | G | A | 1 | a0001c0001t0062g0167 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.249+383C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71710029 | |||||||
chr3:71710054 | CAGAGGCA others(3): Show |
C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0066 others(28): Show |
32 | HG01074.hp1 HG01884.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.249+348_249+357del others(10): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71710054 | |||||||
chr3:71710063 | A | G | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+349T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71710063 | |||||||
chr3:71710076 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.249+336G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71710076 | |||||||
chr3:71710168 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.249+244T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71710168 | |||||||
chr3:71710243 | G | A | 1 | a0001c0001t0054g0168 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.249+169C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71710243 | |||||||
chr3:71710395 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.249+17G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 2/6 | chr3 | 71710395 | |||||||
chr3:71710554 | T | G | 1 | a0001c0001t0002g0360 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177-70A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71710554 | |||||||
chr3:71710566 | C | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(161): Show |
173 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.177-82G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71710566 | |||||||
chr3:71710569 | C | G | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.177-85G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71710569 | |||||||
chr3:71710657 | G | T | 3 | a0001c0001t0001g0297 a0001c0001t0003g0210 a0001c0001t0070g0130 |
3 | HG03239.hp2 HG04204.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.177-173C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71710657 | |||||||
chr3:71710703 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.177-219T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71710703 | |||||||
chr3:71710869 | C | A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177-385G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71710869 | |||||||
chr3:71710890 | C | A | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.177-406G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71710890 | |||||||
chr3:71711244 | T | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0032 others(82): Show |
95 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.177-760A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711244 | |||||||
chr3:71711371 | G | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(163): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.177-887C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711371 | |||||||
chr3:71711436 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0229 |
2 | NA18990.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.177-952C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711436 | |||||||
chr3:71711455 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(84): Show |
93 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.177-971G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711455 | |||||||
chr3:71711583 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.177-1099C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711583 | |||||||
chr3:71711603 | T | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0106 others(30): Show |
34 | HG00621.hp1 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.177-1119A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711603 | |||||||
chr3:71711659 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0036 others(84): Show |
93 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.177-1175G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711659 | |||||||
chr3:71711702 | C | T | 7 | a0001c0001t0003g0126 a0001c0001t0003g0330 a0001c0001t0006g0122 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.177-1218G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711702 | |||||||
chr3:71711724 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(254): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.177-1240G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711724 | |||||||
chr3:71711811 | T | A | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | HG01167.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.177-1327A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711811 | |||||||
chr3:71711839 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.177-1355G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711839 | |||||||
chr3:71711891 | G | A | 1 | a0001c0001t0013g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177-1407C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711891 | |||||||
chr3:71711938 | G | A | 1 | a0001c0001t0008g0327 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.177-1454C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71711938 | |||||||
chr3:71712233 | C | A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177-1749G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712233 | |||||||
chr3:71712298 | C | T | 6 | a0001c0001t0001g0297 a0001c0001t0003g0210 a0001c0001t0003g0362 others(3): Show |
6 | HG01175.hp2 HG02523.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.177-1814G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712298 | |||||||
chr3:71712347 | A | G | 2 | a0001c0001t0006g0302 a0001c0001t0044g0207 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.177-1863T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712347 | |||||||
chr3:71712385 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.177-1901T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712385 | |||||||
chr3:71712403 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(262): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.177-1919A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712403 | |||||||
chr3:71712450 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(221): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.177-1966A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712450 | |||||||
chr3:71712476 | T | G | 2 | a0001c0001t0006g0302 a0001c0001t0044g0207 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.177-1992A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712476 | |||||||
chr3:71712585 | T | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(120): Show |
128 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.177-2101A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712585 | |||||||
chr3:71712635 | T | TG | 65 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(62): Show |
69 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.177-2152dupC | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712635 | |||||||
chr3:71712635 | T | TGG | 70 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0036 others(67): Show |
75 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.177-2153_177-2152d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712635 | |||||||
chr3:71712635 | T | TGGG | 16 | a0001c0001t0001g0041 a0001c0001t0001g0184 a0001c0001t0001g0312 others(13): Show |
16 | HG00673.hp1 HG01167.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.177-2154_177-2152d others(5): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712635 | |||||||
chr3:71712639 | C | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(257): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.177-2155G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712639 | |||||||
chr3:71712644 | G | GC | 98 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(95): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.177-2161_177-2160i others(3): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712644 | |||||||
chr3:71712708 | T | C | 1 | a0001c0001t0003g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.177-2224A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712708 | |||||||
chr3:71712852 | C | CA | 184 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.177-2369dupT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712852 | |||||||
chr3:71712852 | C | CAA | 8 | a0001c0001t0001g0285 a0001c0001t0002g0172 a0001c0001t0004g0133 others(5): Show |
8 | HG01515.hp2 HG01934.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.177-2370_177-2369d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712852 | |||||||
chr3:71712852 | CA | C | 39 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(36): Show |
39 | HG01167.hp2 HG01175.hp2 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.177-2369delT | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712852 | |||||||
chr3:71712852 | CAA | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(30): Show |
36 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.177-2370_177-2369d others(4): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712852 | |||||||
chr3:71712945 | T | G | 1 | a0001c0001t0002g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.177-2461A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71712945 | |||||||
chr3:71713020 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.177-2536G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713020 | |||||||
chr3:71713138 | A | G | 5 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0311 others(2): Show |
5 | HG01167.hp1 HG01255.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.177-2654T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713138 | |||||||
chr3:71713278 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.177-2794C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713278 | |||||||
chr3:71713501 | ATCATAGC | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(40): Show |
46 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.177-3024_177-3018d others(9): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713501 | |||||||
chr3:71713576 | A | G | 1 | a0001c0001t0004g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.177-3092T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713576 | |||||||
chr3:71713644 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0038 others(12): Show |
17 | HG00673.hp1 HG01109.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.177-3160G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713644 | |||||||
chr3:71713851 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(40): Show |
46 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.177-3367C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713851 | |||||||
chr3:71713873 | T | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0201 others(11): Show |
14 | HG01361.hp1 HG01952.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.177-3389A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71713873 | |||||||
chr3:71714026 | A | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(41): Show |
47 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.177-3542T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714026 | |||||||
chr3:71714143 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.177-3659G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714143 | |||||||
chr3:71714234 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(181): Show |
193 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.177-3750C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714234 | |||||||
chr3:71714240 | GGAAA | G | 12 | a0001c0001t0001g0217 a0001c0001t0001g0231 a0001c0001t0002g0214 others(9): Show |
12 | HG01993.hp2 HG02145.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.177-3760_177-3757d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714240 | |||||||
chr3:71714240 | GGAAAGGA others(1): Show |
G | 5 | a0001c0001t0001g0106 a0001c0001t0001g0213 a0001c0001t0003g0029 others(2): Show |
5 | HG01934.hp2 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.177-3764_177-3757d others(10): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714240 | |||||||
chr3:71714240 | GGAAAGGA others(5): Show |
G | 3 | a0001c0001t0006g0302 a0001c0001t0012g0212 a0001c0001t0044g0207 |
3 | HG02071.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.177-3768_177-3757d others(14): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714240 | |||||||
chr3:71714240 | GGAAAGGA others(13): Show |
G | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.177-3776_177-3757d others(22): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714240 | |||||||
chr3:71714242 | A | G | 21 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(18): Show |
24 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.177-3758T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714242 | |||||||
chr3:71714249 | GGAAGGAA others(17): Show |
G | 3 | a0001c0001t0001g0021 a0001c0001t0030g0020 a0001c0001t0032g0019 |
3 | HG02257.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.177-3789_177-3766d others(26): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714249 | |||||||
chr3:71714250 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(11): Show |
17 | HG00597.hp2 HG00621.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.177-3766C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714250 | |||||||
chr3:71714253 | GGAAGGAA others(13): Show |
G | 59 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0201 others(56): Show |
61 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.177-3789_177-3770d others(22): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714253 | |||||||
chr3:71714254 | G | A | 11 | a0001c0001t0001g0217 a0001c0001t0001g0231 a0001c0001t0002g0214 others(8): Show |
11 | HG01993.hp2 HG02886.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.177-3770C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714254 | |||||||
chr3:71714257 | GGAAGGAA others(9): Show |
G | 25 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0292 others(22): Show |
27 | HG00280.hp1 HG01884.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.177-3789_177-3774d others(18): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714257 | |||||||
chr3:71714258 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0213 a0001c0001t0003g0029 |
3 | HG01934.hp2 HG02109.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.177-3774C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714258 | |||||||
chr3:71714261 | GGAAGGAA others(5): Show |
G | 15 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0112 others(12): Show |
15 | HG00609.hp1 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.177-3789_177-3778d others(14): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714261 | |||||||
chr3:71714262 | G | A | 3 | a0001c0001t0006g0302 a0001c0001t0012g0212 a0001c0001t0044g0207 |
3 | HG02071.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.177-3778C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714262 | |||||||
chr3:71714265 | GGAAGGAA others(1): Show |
G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0116 others(2): Show |
5 | HG01109.hp1 HG02165.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.177-3789_177-3782d others(10): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714265 | |||||||
chr3:71714269 | G | A | 1 | a0001c0001t0023g0295 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.177-3785C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714269 | |||||||
chr3:71714269 | G | C | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177-3785C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714269 | |||||||
chr3:71714269 | GGAAA | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0184 others(9): Show |
13 | HG00639.hp2 HG00673.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.177-3789_177-3786d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714269 | |||||||
chr3:71714273 | A | AGAAG | 64 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0138 others(61): Show |
71 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.177-3793_177-3790d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714273 | |||||||
chr3:71714273 | A | AGAAGGAA others(1): Show |
5 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0002g0189 others(2): Show |
6 | HG02027.hp1 HG03704.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.177-3797_177-3790d others(10): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714273 | |||||||
chr3:71714273 | A | C | 11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0308 others(8): Show |
11 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.177-3789T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714273 | |||||||
chr3:71714273 | A | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0038 others(55): Show |
61 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.177-3789T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714273 | |||||||
chr3:71714273 | AGAAG | A | 5 | a0001c0001t0001g0198 a0001c0001t0001g0267 a0001c0001t0002g0200 others(2): Show |
5 | HG01358.hp2 HG01975.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.177-3793_177-3790d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714273 | |||||||
chr3:71714273 | AGAAGGAA others(5): Show |
A | 1 | a0001c0001t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.177-3801_177-3790d others(14): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714273 | |||||||
chr3:71714277 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177-3793C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714277 | |||||||
chr3:71714277 | GGAAGGAA others(21): Show |
G | 10 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0308 others(7): Show |
10 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.177-3821_177-3794d others(30): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714277 | |||||||
chr3:71714279 | AAGGAAGG others(20): Show |
A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177-3822_177-3796d others(29): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714279 | |||||||
chr3:71714281 | G | A | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.177-3797C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714281 | |||||||
chr3:71714283 | AAGGAAGG others(16): Show |
A | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.177-3822_177-3800d others(25): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714283 | |||||||
chr3:71714301 | G | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0038 others(97): Show |
106 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.177-3817C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714301 | |||||||
chr3:71714301 | G | GGAAGGAA others(5): Show |
1 | a0001c0001t0001g0365 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.177-3818_177-3817i others(14): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714301 | |||||||
chr3:71714305 | C | CGAACGAA others(1): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(31): Show |
37 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.177-3822_177-3821i others(10): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714305 | |||||||
chr3:71714305 | C | CGAAG | 8 | a0001c0001t0001g0041 a0001c0001t0001g0239 a0001c0001t0003g0126 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.177-3822_177-3821i others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714305 | |||||||
chr3:71714305 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0038 others(98): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.177-3821G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714305 | |||||||
chr3:71714309 | A | G | 2 | a0001c0001t0003g0330 a0001c0001t0074g0328 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.177-3825T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714309 | |||||||
chr3:71714323 | A | AG | 34 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(31): Show |
37 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.177-3840dupC | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714323 | |||||||
chr3:71714329 | A | AAAG | 13 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0308 others(10): Show |
13 | HG01167.hp1 HG01255.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.177-3848_177-3846d others(5): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714329 | |||||||
chr3:71714500 | C | T | 1 | a0001c0001t0011g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.177-4016G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714500 | |||||||
chr3:71714501 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.177-4017C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714501 | |||||||
chr3:71714563 | C | A | 1 | a0001c0001t0002g0360 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177-4079G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714563 | |||||||
chr3:71714604 | C | T | 2 | a0001c0001t0001g0348 a0001c0001t0009g0344 |
2 | HG01081.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.177-4120G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714604 | |||||||
chr3:71714616 | C | A | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0311 others(1): Show |
4 | HG01167.hp1 HG01255.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.177-4132G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714616 | |||||||
chr3:71714654 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(29): Show |
35 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.177-4170C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714654 | |||||||
chr3:71714723 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.177-4239A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714723 | |||||||
chr3:71714761 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.177-4277G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714761 | |||||||
chr3:71714823 | TGAAGCCT others(4): Show |
T | 1 | a0001c0001t0002g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.177-4350_177-4340d others(13): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714823 | |||||||
chr3:71714953 | A | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(152): Show |
164 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.177-4469T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71714953 | |||||||
chr3:71715008 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(145): Show |
157 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.177-4524G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715008 | |||||||
chr3:71715020 | C | A | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0311 others(1): Show |
4 | HG01167.hp1 HG01255.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.177-4536G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715020 | |||||||
chr3:71715040 | C | T | 8 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0308 others(5): Show |
8 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.177-4556G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715040 | |||||||
chr3:71715045 | T | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(145): Show |
157 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.177-4561A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715045 | |||||||
chr3:71715087 | G | T | 2 | a0001c0001t0004g0131 a0001c0001t0024g0132 |
2 | NA18988.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177-4603C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715087 | |||||||
chr3:71715147 | T | C | 1 | a0001c0001t0040g0186 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.177-4663A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715147 | |||||||
chr3:71715286 | A | G | 1 | a0001c0001t0002g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.177-4802T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715286 | |||||||
chr3:71715348 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.177-4864C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715348 | |||||||
chr3:71715379 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0038 others(109): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.177-4895A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715379 | |||||||
chr3:71715426 | G | A | 1 | a0001c0001t0002g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.177-4942C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715426 | |||||||
chr3:71715428 | A | T | 1 | a0001c0001t0002g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.177-4944T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715428 | |||||||
chr3:71715430 | T | C | 1 | a0001c0001t0002g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.177-4946A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715430 | |||||||
chr3:71715466 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0003g0233 a0001c0001t0006g0232 |
3 | HG02258.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.177-4982T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715466 | |||||||
chr3:71715652 | G | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(178): Show |
189 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.177-5168C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715652 | |||||||
chr3:71715739 | TTAA | T | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.177-5258_177-5256d others(5): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715739 | |||||||
chr3:71715939 | T | C | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.177-5455A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715939 | |||||||
chr3:71715960 | T | G | 3 | a0001c0001t0011g0065 a0001c0001t0011g0097 a0001c0001t0011g0109 |
3 | HG00642.hp2 HG01081.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.177-5476A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71715960 | |||||||
chr3:71716081 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.177-5597G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716081 | |||||||
chr3:71716140 | G | A | 1 | a0001c0001t0038g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.177-5656C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716140 | |||||||
chr3:71716238 | CT | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(31): Show |
37 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.177-5755delA | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716238 | |||||||
chr3:71716442 | C | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0292 a0001c0001t0001g0318 |
3 | HG01952.hp1 HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.177-5958G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716442 | |||||||
chr3:71716518 | C | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0201 others(14): Show |
17 | HG01361.hp1 HG01952.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.177-6034G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716518 | |||||||
chr3:71716553 | T | TCCAGAAA others(6): Show |
1 | a0001c0001t0007g0090 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.177-6082_177-6070d others(15): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716553 | |||||||
chr3:71716631 | G | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(31): Show |
37 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.177-6147C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716631 | |||||||
chr3:71716665 | C | A | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.177-6181G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716665 | |||||||
chr3:71716860 | G | A | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.177-6376C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716860 | |||||||
chr3:71716903 | C | A | 3 | a0001c0001t0001g0103 a0001c0001t0008g0102 a0001c0001t0029g0104 |
3 | HG02647.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.177-6419G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716903 | |||||||
chr3:71716943 | G | T | 1 | a0001c0001t0003g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177-6459C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716943 | |||||||
chr3:71716945 | T | A | 3 | a0001c0001t0001g0329 a0001c0001t0006g0304 a0001c0001t0006g0305 |
3 | HG02630.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.177-6461A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716945 | |||||||
chr3:71716953 | C | G | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177-6469G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71716953 | |||||||
chr3:71717047 | C | G | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0308 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177-6563G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717047 | |||||||
chr3:71717147 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.177-6663G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717147 | |||||||
chr3:71717224 | C | G | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177-6740G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717224 | |||||||
chr3:71717301 | G | A | 34 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(31): Show |
34 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.177-6817C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717301 | |||||||
chr3:71717464 | G | A | 31 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(28): Show |
31 | HG01175.hp2 HG01361.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.177-6980C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717464 | |||||||
chr3:71717536 | A | G | 10 | a0001c0001t0001g0329 a0001c0001t0003g0126 a0001c0001t0003g0330 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.177-7052T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717536 | |||||||
chr3:71717618 | C | T | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.177-7134G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717618 | |||||||
chr3:71717705 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0065g0058 |
5 | HG01109.hp1 HG01928.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.177-7221A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717705 | |||||||
chr3:71717725 | T | C | 1 | a0001c0001t0050g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.177-7241A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717725 | |||||||
chr3:71717840 | A | C | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.176+7352T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717840 | |||||||
chr3:71717849 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
90 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.176+7343A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717849 | |||||||
chr3:71717920 | G | A | 5 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(2): Show |
5 | NA18940.hp1 NA18945.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.176+7272C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717920 | |||||||
chr3:71717943 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.176+7249A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71717943 | |||||||
chr3:71718072 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.176+7120G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718072 | |||||||
chr3:71718100 | C | G | 1 | a0001c0001t0003g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.176+7092G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718100 | |||||||
chr3:71718155 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(40): Show |
46 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.176+7037T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718155 | |||||||
chr3:71718165 | G | C | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.176+7027C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718165 | |||||||
chr3:71718213 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.176+6979C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718213 | |||||||
chr3:71718229 | A | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(29): Show |
35 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.176+6963T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718229 | |||||||
chr3:71718262 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(172): Show |
183 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.176+6930G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718262 | |||||||
chr3:71718273 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.176+6919G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718273 | |||||||
chr3:71718274 | G | A | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.176+6918C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718274 | |||||||
chr3:71718348 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(25): Show |
31 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.176+6844A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718348 | |||||||
chr3:71718527 | T | G | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.176+6665A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718527 | |||||||
chr3:71718627 | G | A | 1 | a0001c0001t0073g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.176+6565C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718627 | |||||||
chr3:71718696 | A | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0364 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.176+6496T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718696 | |||||||
chr3:71718883 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.176+6309C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718883 | |||||||
chr3:71718927 | T | C | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.176+6265A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71718927 | |||||||
chr3:71719043 | A | G | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176+6149T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719043 | |||||||
chr3:71719280 | T | G | 1 | a0001c0001t0002g0178 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.176+5912A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719280 | |||||||
chr3:71719322 | T | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(177): Show |
188 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.176+5870A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719322 | |||||||
chr3:71719348 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0038 others(87): Show |
95 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.176+5844G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719348 | |||||||
chr3:71719536 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0067g0334 |
2 | HG01070.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.176+5656T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719536 | |||||||
chr3:71719619 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(177): Show |
188 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.176+5573T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719619 | |||||||
chr3:71719660 | C | T | 2 | a0001c0001t0003g0362 a0001c0001t0031g0361 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.176+5532G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719660 | |||||||
chr3:71719684 | T | C | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.176+5508A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719684 | |||||||
chr3:71719716 | T | C | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176+5476A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719716 | |||||||
chr3:71719818 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.176+5374C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719818 | |||||||
chr3:71719831 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(87): Show |
93 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.176+5361G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71719831 | |||||||
chr3:71720014 | A | AATAT | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.176+5174_176+5177d others(6): Show |
EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720014 | |||||||
chr3:71720014 | A | T | 1 | a0001c0001t0003g0237 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.176+5178T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720014 | |||||||
chr3:71720051 | T | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0114 |
3 | HG01891.hp2 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.176+5141A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720051 | |||||||
chr3:71720105 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(25): Show |
31 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.176+5087A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720105 | |||||||
chr3:71720180 | A | G | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176+5012T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720180 | |||||||
chr3:71720181 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(31): Show |
37 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.176+5011G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720181 | |||||||
chr3:71720286 | T | C | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(282): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.176+4906A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720286 | |||||||
chr3:71720460 | A | G | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.176+4732T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720460 | |||||||
chr3:71720483 | C | A | 3 | a0001c0001t0001g0329 a0001c0001t0006g0304 a0001c0001t0006g0305 |
3 | HG02630.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.176+4709G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720483 | |||||||
chr3:71720565 | G | C | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.176+4627C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720565 | |||||||
chr3:71720686 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0003g0018 a0001c0001t0003g0070 others(1): Show |
4 | HG02486.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.176+4506A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720686 | |||||||
chr3:71720705 | G | A | 10 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0297 others(7): Show |
10 | HG01175.hp2 HG01891.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.176+4487C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720705 | |||||||
chr3:71720753 | A | G | 2 | a0001c0001t0003g0330 a0001c0001t0015g0331 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.176+4439T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720753 | |||||||
chr3:71720846 | G | C | 1 | a0001c0001t0002g0291 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.176+4346C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720846 | |||||||
chr3:71720871 | G | C | 6 | a0001c0001t0003g0126 a0001c0001t0006g0122 a0001c0001t0006g0123 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.176+4321C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720871 | |||||||
chr3:71720877 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.176+4315C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720877 | |||||||
chr3:71720971 | T | A | 1 | a0001c0001t0007g0090 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.176+4221A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720971 | |||||||
chr3:71720992 | G | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0098 others(29): Show |
35 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.176+4200C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71720992 | |||||||
chr3:71721036 | T | G | 42 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0112 others(39): Show |
42 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.176+4156A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721036 | |||||||
chr3:71721037 | A | G | 2 | a0001c0001t0003g0330 a0001c0001t0015g0331 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.176+4155T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721037 | |||||||
chr3:71721049 | G | A | 1 | a0001c0001t0002g0360 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.176+4143C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721049 | |||||||
chr3:71721123 | A | T | 1 | a0001c0001t0007g0090 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.176+4069T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721123 | |||||||
chr3:71721138 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.176+4054C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721138 | |||||||
chr3:71721251 | C | T | 1 | a0001c0001t0003g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.176+3941G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721251 | |||||||
chr3:71721254 | A | G | 2 | a0001c0001t0003g0330 a0001c0001t0015g0331 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.176+3938T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721254 | |||||||
chr3:71721351 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.176+3841T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721351 | |||||||
chr3:71721500 | G | A | 1 | a0001c0001t0046g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.176+3692C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721500 | |||||||
chr3:71721551 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.176+3641C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721551 | |||||||
chr3:71721585 | G | C | 1 | a0001c0001t0003g0298 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.176+3607C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721585 | |||||||
chr3:71721610 | T | C | 10 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0308 others(7): Show |
10 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.176+3582A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721610 | |||||||
chr3:71721684 | C | T | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0308 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.176+3508G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721684 | |||||||
chr3:71721976 | C | T | 1 | a0001c0001t0044g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.176+3216G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721976 | |||||||
chr3:71721991 | AG | A | 22 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0003g0006 others(19): Show |
23 | HG00609.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.176+3200delC | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71721991 | |||||||
chr3:71722029 | G | C | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.176+3163C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722029 | |||||||
chr3:71722064 | T | TG | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(237): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.176+3127dupC | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722064 | |||||||
chr3:71722093 | C | CG | 55 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0072 others(52): Show |
56 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.176+3098dupC | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722093 | |||||||
chr3:71722142 | G | A | 1 | a0001c0001t0005g0301 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.176+3050C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722142 | |||||||
chr3:71722148 | C | T | 1 | a0001c0001t0011g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.176+3044G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722148 | |||||||
chr3:71722179 | T | C | 10 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0003g0311 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.176+3013A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722179 | |||||||
chr3:71722303 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.176+2889A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722303 | |||||||
chr3:71722308 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0032 others(50): Show |
57 | HG00408.hp1 HG01074.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.176+2884G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722308 | |||||||
chr3:71722403 | G | C | 2 | a0001c0001t0003g0084 a0001c0001t0022g0085 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.176+2789C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722403 | |||||||
chr3:71722441 | C | T | 1 | a0001c0001t0026g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.176+2751G>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722441 | |||||||
chr3:71722445 | C | A | 1 | a0001c0001t0001g0313 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.176+2747G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722445 | |||||||
chr3:71722446 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0314 a0001c0001t0001g0315 |
4 | NA18971.hp2 NA19056.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.176+2746C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722446 | |||||||
chr3:71722597 | G | A | 3 | a0001c0001t0003g0317 a0001c0001t0003g0330 a0001c0001t0005g0316 |
3 | HG02723.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.176+2595C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722597 | |||||||
chr3:71722752 | A | T | 1 | a0001c0001t0007g0090 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.176+2440T>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722752 | |||||||
chr3:71722832 | T | A | 1 | a0001c0001t0007g0090 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.176+2360A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722832 | |||||||
chr3:71722861 | A | C | 1 | a0001c0001t0007g0090 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.176+2331T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722861 | |||||||
chr3:71722929 | A | C | 3 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0008g0327 |
3 | HG01167.hp1 HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.176+2263T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722929 | |||||||
chr3:71722996 | A | C | 1 | a0001c0001t0028g0022 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.176+2196T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71722996 | |||||||
chr3:71723250 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0318 a0001c0001t0001g0319 others(5): Show |
9 | HG01346.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.176+1942C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723250 | |||||||
chr3:71723313 | T | G | 3 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0008g0327 |
3 | HG01167.hp1 HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.176+1879A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723313 | |||||||
chr3:71723369 | T | A | 1 | a0001c0001t0074g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.176+1823A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723369 | |||||||
chr3:71723467 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0027 others(70): Show |
78 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.176+1725A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723467 | |||||||
chr3:71723486 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(75): Show |
83 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.176+1706A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723486 | |||||||
chr3:71723489 | T | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(75): Show |
83 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.176+1703A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723489 | |||||||
chr3:71723730 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0003g0330 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.176+1462A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723730 | |||||||
chr3:71723887 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.176+1305A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723887 | |||||||
chr3:71723932 | T | C | 2 | a0001c0001t0003g0362 a0001c0001t0031g0361 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.176+1260A>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723932 | |||||||
chr3:71723990 | A | C | 1 | a0001c0001t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.176+1202T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71723990 | |||||||
chr3:71724064 | G | A | 1 | a0001c0001t0015g0331 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176+1128C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724064 | |||||||
chr3:71724123 | A | G | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(333): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.176+1069T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724123 | |||||||
chr3:71724226 | T | G | 1 | a0001c0001t0001g0363 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.176+966A>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724226 | |||||||
chr3:71724319 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.176+873C>A | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724319 | |||||||
chr3:71724374 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.176+818T>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724374 | |||||||
chr3:71724521 | G | C | 1 | a0001c0001t0001g0364 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.176+671C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724521 | |||||||
chr3:71724551 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.176+641G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724551 | |||||||
chr3:71724563 | G | C | 1 | a0001c0001t0001g0365 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.176+629C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724563 | |||||||
chr3:71724607 | T | A | 1 | a0001c0001t0002g0366 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.176+585A>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724607 | |||||||
chr3:71724862 | C | A | 1 | a0001c0001t0007g0367 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.176+330G>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724862 | |||||||
chr3:71724884 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.176+308G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724884 | |||||||
chr3:71724919 | G | C | 2 | a0001c0001t0001g0368 a0001c0001t0001g0369 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.176+273C>G | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71724919 | |||||||
chr3:71725079 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(75): Show |
83 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.176+113T>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71725079 | |||||||
chr3:71725157 | C | G | 1 | a0001c0001t0001g0005 | 2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.176+35G>C | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71725157 | |||||||
chr3:71725182 | G | A | 5 | a0001c0001t0004g0370 a0001c0001t0004g0371 a0001c0001t0004g0372 others(2): Show |
5 | NA18943.hp1 NA18944.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.176+10C>T | EIF4E3 | ENSG00000163412.13 | transcript | ENST00000425534.8 | protein_coding | 1/6 | chr3 | 71725182 |