Item | Value |
---|---|
geneid | 54756 |
ensemblid | ENSG00000144730.19 |
hgncid | 17616 |
symbol | IL17RD |
name | interleukin 17 receptor D |
refseq_nuc | NM_017563.5 |
refseq_prot | NP_060033.3 |
ensembl_nuc | ENST00000296318.12 |
ensembl_prot | ENSP00000296318.7 |
mane_status | MANE Select |
chr | chr3 |
start | 57089982 |
end | 57165353 |
strand | - |
ver | v1.2 |
region | chr3:57089982-57165353 |
region5000 | chr3:57084982-57170353 |
regionname0 | IL17RD_chr3_57089982_57165353 |
regionname5000 | IL17RD_chr3_57084982_57170353 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 739 | 137 | 38 | 37 | 24 | 7 | 30 | 20 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0002 | 1/0 | 739 | 107 | 36 | 7 | 60 | 1 | 2 | 47 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0003 | 0/0 | 739 | 90 | 5 | 21 | 55 | 1 | 8 | 44 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0004 | 0/0 | 739 | 9 | 5 | 3 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0005 | 0/0 | 739 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0006 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0007 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | MSPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0008 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0009 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
a0010 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | MAPWL others(734): Show |
chr3 | 57084982 | 57170353 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2217 | 130 | 32 | 37 | 24 | 7 | 29 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0001c0006 | 0/0 | 2217 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0001c0013 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0002c0003 | 1/0 | 2217 | 82 | 20 | 4 | 56 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0002c0004 | 0/0 | 2217 | 17 | 10 | 3 | 2 | 1 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0002c0007 | 0/0 | 2217 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0002c0012 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0002c0015 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0003c0002 | 0/0 | 2217 | 88 | 5 | 21 | 53 | 1 | 8 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0003c0010 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0003c0011 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0004c0008 | 0/0 | 2217 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0004c0009 | 0/0 | 2217 | 4 | 1 | 2 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0005c0005 | 0/0 | 2217 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0006c0014 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0007c0019 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGTC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0008c0017 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0009c0016 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 | ||
a0010c0018 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ATGGC others(2212): Show |
chr3 | 57084982 | 57170353 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 8697 | 35 | 8 | 9 | 12 | 3 | 3 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0004 | 0/1 | 8697 | 29 | 7 | 12 | 2 | 1 | 6 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0005 | 0/0 | 8697 | 18 | 0 | 3 | 7 | 1 | 7 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0006 | 0/0 | 8697 | 9 | 9 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0007 | 0/0 | 8697 | 12 | 0 | 5 | 0 | 1 | 6 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0018 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0020 | 0/0 | 8697 | 2 | 0 | 1 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0024 | 0/0 | 8697 | 2 | 1 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0025 | 0/0 | 8697 | 2 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0026 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0027 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0028 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0029 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0033 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0034 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0035 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0036 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0037 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0038 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0039 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0040 | 0/0 | 8698 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0042 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0043 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0044 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0045 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0046 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0047 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0052 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0001t0056 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0006t0011 | 0/0 | 8697 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0001c0013t0004 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0002 | 1/0 | 8698 | 58 | 2 | 1 | 53 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0012 | 0/0 | 8698 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0013 | 0/0 | 8698 | 5 | 5 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0014 | 0/0 | 8697 | 4 | 3 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0021 | 0/0 | 8697 | 2 | 1 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0022 | 0/0 | 8698 | 2 | 2 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0030 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0031 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0032 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8694): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0053 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0054 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0003t0055 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0008 | 0/0 | 8698 | 7 | 0 | 3 | 2 | 1 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0016 | 0/0 | 8698 | 3 | 3 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0019 | 0/0 | 8698 | 2 | 2 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0048 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0049 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0050 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0051 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0004t0057 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0002c0007t0009 | 0/0 | 8698 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0012t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0002c0015t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0003c0002t0001 | 0/0 | 8699 | 81 | 3 | 20 | 50 | 1 | 7 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8694): Show |
chr3 | 57084982 | 57170353 |
a0003c0002t0015 | 0/0 | 8698 | 3 | 2 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0003c0002t0017 | 0/0 | 8699 | 2 | 0 | 0 | 1 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8694): Show |
chr3 | 57084982 | 57170353 |
a0003c0002t0023 | 0/0 | 8699 | 2 | 0 | 0 | 2 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8694): Show |
chr3 | 57084982 | 57170353 |
a0003c0010t0041 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8694): Show |
chr3 | 57084982 | 57170353 |
a0003c0011t0001 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8694): Show |
chr3 | 57084982 | 57170353 |
a0004c0008t0006 | 0/0 | 8697 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0004c0009t0003 | 0/0 | 8697 | 4 | 1 | 2 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0005c0005t0010 | 0/0 | 8697 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0006c0014t0018 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0007c0019t0003 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
a0008c0017t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0009c0016t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8693): Show |
chr3 | 57084982 | 57170353 |
a0010c0018t0003 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | ACTCG others(8692): Show |
chr3 | 57084982 | 57170353 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0018g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0020g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0020g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0024g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0024g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0025g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0025g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0026g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0027g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0028g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0029g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0033g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0034g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0035g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0036g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0037g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0038g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0039g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0040g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0042g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0043g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0044g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0045g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0046g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0047g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0052g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0001t0056g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0006t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0006t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0006t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0006t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0006t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0006t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0001c0013t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0255 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0012g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0013g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0013g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0013g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0014g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0014g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0014g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0021g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0021g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0022g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0022g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0030g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0031g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0032g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0053g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0054g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0003t0055g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0008g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0008g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0008g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0008g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0008g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0016g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0016g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0016g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0048g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0049g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0050g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0051g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0004t0057g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0007t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0007t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0007t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0007t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0007t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0007t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0012t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0002c0015t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0015g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0015g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0017g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0017g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0002t0023g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0010t0041g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0003c0011t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0008t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0008t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0008t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0008t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0008t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0009t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0009t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0009t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0004c0009t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0005c0005t0010g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0005c0005t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0005c0005t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0005c0005t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0005c0005t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0005c0005t0010g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0006c0014t0018g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0007c0019t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0008c0017t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0009c0016t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
a0010c0018t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0004 | t0008 | g0298 | EUR | GBR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0228 | EUR | GBR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0249 | EUR | FIN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0032 | EUR | FIN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00544 | hp1 | a0002 | c0003 | t0002 | g0088 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00544 | hp2 | a0002 | c0003 | t0002 | g0316 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00558 | hp1 | a0003 | c0002 | t0001 | g0174 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00558 | hp2 | a0002 | c0003 | t0032 | g0303 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00609 | hp1 | a0002 | c0012 | t0002 | g0192 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00639 | hp1 | a0002 | c0004 | t0008 | g0322 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00639 | hp2 | a0003 | c0002 | t0001 | g0049 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00642 | hp1 | a0003 | c0002 | t0001 | g0163 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00673 | hp1 | a0002 | c0003 | t0002 | g0098 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00673 | hp2 | a0003 | c0002 | t0001 | g0085 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0208 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01069 | hp1 | a0003 | c0002 | t0001 | g0056 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01069 | hp2 | a0001 | c0001 | t0026 | g0267 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01070 | hp1 | a0002 | c0003 | t0002 | g0294 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01071 | hp2 | a0003 | c0002 | t0001 | g0057 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01074 | hp1 | a0003 | c0002 | t0001 | g0148 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01074 | hp2 | a0004 | c0009 | t0003 | g0247 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01081 | hp1 | a0003 | c0002 | t0001 | g0070 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01081 | hp2 | a0001 | c0001 | t0047 | g0198 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01099 | hp1 | a0001 | c0001 | t0056 | g0246 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01099 | hp2 | a0002 | c0004 | t0008 | g0264 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01106 | hp1 | a0001 | c0001 | t0020 | g0022 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01106 | hp2 | a0003 | c0002 | t0001 | g0162 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01109 | hp1 | a0003 | c0002 | t0001 | g0169 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01109 | hp2 | a0002 | c0003 | t0014 | g0172 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01169 | hp2 | a0003 | c0002 | t0015 | g0290 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01192 | hp2 | a0003 | c0002 | t0001 | g0139 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01243 | hp1 | a0001 | c0001 | t0052 | g0299 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01243 | hp2 | a0004 | c0008 | t0006 | g0044 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01255 | hp1 | a0002 | c0003 | t0012 | g0156 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0240 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01256 | hp2 | a0003 | c0002 | t0001 | g0079 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0292 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01257 | hp2 | a0001 | c0001 | t0025 | g0345 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0003 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01346 | hp2 | a0002 | c0004 | t0008 | g0215 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0161 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0003 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01361 | hp1 | a0001 | c0001 | t0029 | g0164 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0224 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01433 | hp2 | a0004 | c0009 | t0003 | g0248 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0291 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01496 | hp2 | a0003 | c0002 | t0001 | g0297 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01516 | hp1 | a0001 | c0001 | t0020 | g0212 | EUR | IBS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0223 | EUR | IBS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01884 | hp2 | a0002 | c0004 | t0048 | g0008 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01891 | hp1 | a0002 | c0003 | t0002 | g0093 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01891 | hp2 | a0002 | c0003 | t0012 | g0059 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0160 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01928 | hp2 | a0003 | c0002 | t0001 | g0137 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01934 | hp1 | a0002 | c0003 | t0021 | g0279 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01934 | hp2 | a0003 | c0002 | t0001 | g0052 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01978 | hp1 | a0001 | c0001 | t0040 | g0182 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0152 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01981 | hp2 | a0003 | c0002 | t0001 | g0128 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02027 | hp1 | a0003 | c0002 | t0001 | g0026 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02027 | hp2 | a0003 | c0002 | t0001 | g0030 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02040 | hp1 | a0003 | c0002 | t0001 | g0125 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02055 | hp1 | a0005 | c0005 | t0010 | g0062 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02055 | hp2 | a0004 | c0009 | t0003 | g0096 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02074 | hp2 | a0003 | c0002 | t0001 | g0028 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02080 | hp1 | a0003 | c0002 | t0001 | g0133 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02080 | hp2 | a0002 | c0003 | t0002 | g0039 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02083 | hp1 | a0003 | c0010 | t0041 | g0129 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02129 | hp1 | a0002 | c0003 | t0002 | g0042 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02129 | hp2 | a0003 | c0002 | t0001 | g0179 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02132 | hp1 | a0002 | c0003 | t0002 | g0205 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02132 | hp2 | a0002 | c0003 | t0002 | g0092 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02135 | hp1 | a0003 | c0002 | t0001 | g0025 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02135 | hp2 | a0002 | c0003 | t0002 | g0038 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02145 | hp1 | a0001 | c0001 | t0024 | g0344 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02145 | hp2 | a0001 | c0006 | t0011 | g0010 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02148 | hp1 | a0003 | c0002 | t0001 | g0135 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02148 | hp2 | a0001 | c0001 | t0007 | g0151 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02165 | hp1 | a0002 | c0003 | t0002 | g0283 | EAS | CDX | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02165 | hp2 | a0002 | c0015 | t0002 | g0278 | EAS | CDX | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02257 | hp1 | a0002 | c0004 | t0016 | g0341 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02258 | hp1 | a0001 | c0001 | t0046 | g0309 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0317 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02293 | hp1 | a0003 | c0002 | t0001 | g0055 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02293 | hp2 | a0003 | c0002 | t0001 | g0089 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02300 | hp1 | a0003 | c0002 | t0001 | g0136 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02300 | hp2 | a0003 | c0002 | t0001 | g0295 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0257 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02451 | hp2 | a0002 | c0003 | t0013 | g0063 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02622 | hp1 | a0002 | c0003 | t0022 | g0097 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02622 | hp2 | a0002 | c0003 | t0014 | g0323 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02630 | hp1 | a0002 | c0003 | t0012 | g0034 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02630 | hp2 | a0002 | c0003 | t0055 | g0009 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02647 | hp2 | a0002 | c0007 | t0009 | g0312 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02683 | hp2 | a0002 | c0003 | t0002 | g0300 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02717 | hp1 | a0002 | c0003 | t0014 | g0170 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02717 | hp2 | a0002 | c0003 | t0013 | g0324 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0188 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02735 | hp2 | a0003 | c0002 | t0001 | g0117 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02738 | hp1 | a0001 | c0001 | t0007 | g0149 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02738 | hp2 | a0001 | c0001 | t0036 | g0095 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02809 | hp1 | a0002 | c0007 | t0009 | g0310 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0331 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02818 | hp2 | a0002 | c0003 | t0022 | g0216 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02886 | hp1 | a0002 | c0004 | t0016 | g0333 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02886 | hp2 | a0002 | c0007 | t0009 | g0075 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02895 | hp1 | a0003 | c0002 | t0015 | g0220 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0222 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02896 | hp1 | a0003 | c0002 | t0001 | g0146 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02897 | hp1 | a0003 | c0002 | t0015 | g0145 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02897 | hp2 | a0003 | c0002 | t0001 | g0219 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02922 | hp2 | a0002 | c0004 | t0019 | g0006 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02965 | hp1 | a0002 | c0003 | t0012 | g0060 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02965 | hp2 | a0005 | c0005 | t0010 | g0091 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02970 | hp1 | a0002 | c0003 | t0021 | g0340 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02970 | hp2 | a0002 | c0004 | t0016 | g0342 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02976 | hp1 | a0001 | c0006 | t0011 | g0013 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02976 | hp2 | a0002 | c0003 | t0053 | g0171 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03017 | hp1 | a0002 | c0004 | t0008 | g0321 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03017 | hp2 | a0001 | c0001 | t0037 | g0041 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03041 | hp1 | a0002 | c0004 | t0049 | g0168 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03041 | hp2 | a0007 | c0019 | t0003 | g0343 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03098 | hp1 | a0001 | c0001 | t0042 | g0019 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03130 | hp2 | a0001 | c0001 | t0027 | g0167 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03139 | hp1 | a0004 | c0008 | t0006 | g0113 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03195 | hp1 | a0005 | c0005 | t0010 | g0332 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03195 | hp2 | a0001 | c0006 | t0011 | g0011 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03209 | hp1 | a0002 | c0003 | t0012 | g0221 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03225 | hp1 | a0004 | c0008 | t0006 | g0076 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0031 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0165 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03453 | hp1 | a0002 | c0004 | t0019 | g0007 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03453 | hp2 | a0002 | c0003 | t0014 | g0185 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03486 | hp1 | a0002 | c0007 | t0009 | g0183 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03486 | hp2 | a0001 | c0006 | t0011 | g0014 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03490 | hp2 | a0003 | c0002 | t0001 | g0080 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0327 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0207 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03492 | hp1 | a0003 | c0002 | t0001 | g0047 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0328 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03516 | hp2 | a0002 | c0004 | t0057 | g0287 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03540 | hp1 | a0002 | c0003 | t0013 | g0078 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03540 | hp2 | a0001 | c0001 | t0039 | g0268 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03579 | hp1 | a0004 | c0008 | t0006 | g0313 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03579 | hp2 | a0001 | c0001 | t0038 | g0035 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0329 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03669 | hp1 | a0003 | c0002 | t0001 | g0142 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03669 | hp2 | a0001 | c0013 | t0004 | g0141 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03688 | hp1 | a0003 | c0002 | t0001 | g0189 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0159 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03704 | hp1 | a0003 | c0002 | t0001 | g0050 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0153 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03710 | hp1 | a0001 | c0001 | t0025 | g0347 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03710 | hp2 | a0001 | c0001 | t0024 | g0346 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0150 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03834 | hp1 | a0001 | c0001 | t0035 | g0124 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0196 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03927 | hp1 | a0003 | c0002 | t0017 | g0132 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03927 | hp2 | a0001 | c0001 | t0033 | g0071 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG04115 | hp1 | a0001 | c0001 | t0007 | g0121 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0289 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0045 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG04199 | hp2 | a0003 | c0002 | t0001 | g0123 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0245 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18522 | hp2 | a0002 | c0003 | t0013 | g0326 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18747 | hp1 | a0002 | c0003 | t0002 | g0202 | EAS | CHB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18747 | hp2 | a0003 | c0002 | t0001 | g0084 | EAS | CHB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18906 | hp2 | a0004 | c0008 | t0006 | g0110 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18941 | hp1 | a0003 | c0002 | t0001 | g0177 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18943 | hp1 | a0002 | c0003 | t0002 | g0251 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18945 | hp1 | a0002 | c0003 | t0002 | g0068 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18945 | hp2 | a0003 | c0002 | t0001 | g0118 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18946 | hp1 | a0002 | c0004 | t0008 | g0077 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18946 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18947 | hp1 | a0001 | c0001 | t0045 | g0193 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18947 | hp2 | a0002 | c0004 | t0008 | g0320 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18948 | hp1 | a0003 | c0002 | t0001 | g0027 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18948 | hp2 | a0002 | c0003 | t0002 | g0225 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18949 | hp2 | a0003 | c0002 | t0001 | g0127 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18950 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18950 | hp2 | a0002 | c0003 | t0002 | g0094 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18956 | hp2 | a0003 | c0002 | t0001 | g0016 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18957 | hp1 | a0003 | c0002 | t0001 | g0082 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18959 | hp2 | a0002 | c0003 | t0002 | g0276 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18961 | hp2 | a0003 | c0002 | t0001 | g0130 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18962 | hp2 | a0003 | c0002 | t0001 | g0066 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18964 | hp1 | a0003 | c0002 | t0001 | g0143 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18964 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18970 | hp2 | a0003 | c0002 | t0001 | g0131 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18971 | hp1 | a0003 | c0002 | t0001 | g0140 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18973 | hp1 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18973 | hp2 | a0003 | c0002 | t0001 | g0181 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18974 | hp1 | a0002 | c0003 | t0002 | g0337 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18974 | hp2 | a0003 | c0002 | t0001 | g0036 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18975 | hp1 | a0002 | c0003 | t0002 | g0262 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18975 | hp2 | a0003 | c0002 | t0001 | g0176 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18977 | hp1 | a0003 | c0002 | t0001 | g0126 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18977 | hp2 | a0002 | c0003 | t0002 | g0269 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18978 | hp1 | a0002 | c0003 | t0002 | g0308 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18978 | hp2 | a0003 | c0002 | t0001 | g0218 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18980 | hp1 | a0003 | c0002 | t0001 | g0271 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18980 | hp2 | a0002 | c0003 | t0002 | g0301 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18982 | hp1 | a0002 | c0003 | t0031 | g0288 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18982 | hp2 | a0002 | c0003 | t0002 | g0306 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18984 | hp1 | a0003 | c0002 | t0001 | g0180 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18984 | hp2 | a0008 | c0017 | t0002 | g0252 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18989 | hp1 | a0001 | c0001 | t0028 | g0109 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18989 | hp2 | a0003 | c0002 | t0001 | g0065 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18990 | hp1 | a0002 | c0003 | t0002 | g0086 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18992 | hp1 | a0002 | c0003 | t0002 | g0037 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18992 | hp2 | a0003 | c0002 | t0001 | g0178 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18993 | hp1 | a0003 | c0002 | t0023 | g0005 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18995 | hp1 | a0002 | c0003 | t0002 | g0305 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19000 | hp1 | a0003 | c0002 | t0001 | g0081 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19000 | hp2 | a0002 | c0003 | t0002 | g0206 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19001 | hp1 | a0003 | c0002 | t0001 | g0274 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19001 | hp2 | a0002 | c0003 | t0002 | g0155 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19002 | hp1 | a0003 | c0002 | t0023 | g0005 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19002 | hp2 | a0002 | c0003 | t0002 | g0339 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19004 | hp1 | a0002 | c0003 | t0002 | g0195 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19004 | hp2 | a0003 | c0002 | t0001 | g0119 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19005 | hp1 | a0003 | c0011 | t0001 | g0122 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19005 | hp2 | a0002 | c0003 | t0002 | g0304 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19006 | hp1 | a0003 | c0002 | t0001 | g0175 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19006 | hp2 | a0002 | c0003 | t0002 | g0338 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19007 | hp2 | a0002 | c0003 | t0002 | g0242 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19009 | hp1 | a0003 | c0002 | t0001 | g0116 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19009 | hp2 | a0002 | c0003 | t0002 | g0243 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19010 | hp1 | a0002 | c0003 | t0002 | g0203 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19011 | hp1 | a0002 | c0003 | t0002 | g0048 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19011 | hp2 | a0003 | c0002 | t0001 | g0083 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19012 | hp1 | a0002 | c0003 | t0002 | g0335 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19012 | hp2 | a0003 | c0002 | t0001 | g0018 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19030 | hp1 | a0001 | c0001 | t0034 | g0100 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19054 | hp2 | a0002 | c0003 | t0002 | g0238 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19056 | hp1 | a0002 | c0003 | t0002 | g0115 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19056 | hp2 | a0003 | c0002 | t0001 | g0166 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19057 | hp1 | a0002 | c0003 | t0002 | g0040 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19057 | hp2 | a0003 | c0002 | t0001 | g0058 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19063 | hp1 | a0002 | c0003 | t0002 | g0217 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19064 | hp2 | a0002 | c0003 | t0002 | g0134 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19065 | hp1 | a0003 | c0002 | t0001 | g0024 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19065 | hp2 | a0003 | c0002 | t0001 | g0273 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19066 | hp1 | a0002 | c0003 | t0002 | g0302 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19066 | hp2 | a0009 | c0016 | t0002 | g0239 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19067 | hp1 | a0002 | c0003 | t0030 | g0213 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19067 | hp2 | a0003 | c0002 | t0001 | g0138 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19068 | hp1 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19068 | hp2 | a0003 | c0002 | t0001 | g0120 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19075 | hp1 | a0003 | c0002 | t0001 | g0051 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19075 | hp2 | a0002 | c0003 | t0002 | g0108 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19079 | hp1 | a0001 | c0001 | t0044 | g0194 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19079 | hp2 | a0003 | c0002 | t0001 | g0211 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19084 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19084 | hp2 | a0003 | c0002 | t0001 | g0272 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19085 | hp1 | a0002 | c0003 | t0002 | g0064 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19085 | hp2 | a0003 | c0002 | t0001 | g0053 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19086 | hp1 | a0002 | c0003 | t0002 | g0204 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19086 | hp2 | a0003 | c0002 | t0017 | g0087 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19087 | hp1 | a0002 | c0003 | t0002 | g0277 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19087 | hp2 | a0003 | c0002 | t0001 | g0147 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19088 | hp1 | a0003 | c0002 | t0001 | g0173 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19088 | hp2 | a0002 | c0003 | t0002 | g0114 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19090 | hp1 | a0010 | c0018 | t0003 | g0233 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19090 | hp2 | a0003 | c0002 | t0001 | g0054 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA19240 | hp2 | a0002 | c0003 | t0013 | g0325 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20129 | hp1 | a0001 | c0006 | t0011 | g0158 | AFR | ASW | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20129 | hp2 | a0002 | c0007 | t0009 | g0311 | AFR | ASW | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20752 | hp1 | a0003 | c0002 | t0001 | g0296 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20752 | hp2 | a0004 | c0009 | t0003 | g0254 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0186 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0214 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20905 | hp1 | a0001 | c0001 | t0043 | g0154 | SAS | GIH | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0275 | SAS | GIH | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01123 | hp1 | a0003 | c0002 | t0001 | g0029 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02109 | hp1 | a0002 | c0007 | t0009 | g0074 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02109 | hp2 | a0002 | c0004 | t0051 | g0020 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02486 | hp1 | a0006 | c0014 | t0018 | g0330 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02559 | hp1 | a0005 | c0005 | t0010 | g0090 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG02559 | hp2 | a0002 | c0004 | t0050 | g0314 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03471 | hp1 | a0002 | c0003 | t0054 | g0021 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG03471 | hp2 | a0005 | c0005 | t0010 | g0157 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
HG06807 | hp2 | a0003 | c0002 | t0001 | g0144 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20300 | hp1 | a0002 | c0003 | t0002 | g0244 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA20300 | hp2 | a0001 | c0006 | t0011 | g0012 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
NA21309 | hp2 | a0005 | c0005 | t0010 | g0061 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0023 | REF | REF | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
homoSapiens | grch38p0 | a0002 | c0003 | t0002 | g0255 | REF | REF | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57097731 | T | C | 1 | a0009 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.1972A>G | p.Met658Val | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 2039/8698 | 1972/2220 | 658/739 | chr3 | 57097731 | |||
chr3:57097779 | C | G | 1 | a0005 | 6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
missense_variant | MODERATE | c.1924G>C | p.Ala642Pro | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1991/8698 | 1924/2220 | 642/739 | chr3 | 57097779 | |||
chr3:57098006 | G | A | 1 | a0004 | 5 | HG01243.hp2 HG03139.hp1 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.1697C>T | p.Pro566Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1764/8698 | 1697/2220 | 566/739 | chr3 | 57098006 | |||
chr3:57098007 | G | A | 1 | a0004 | 4 | HG01074.hp2 HG01433.hp2 HG02055.hp2 others(1): Show |
missense_variant | MODERATE | c.1696C>T | p.Pro566Ser | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1763/8698 | 1696/2220 | 566/739 | chr3 | 57098007 | |||
chr3:57101356 | T | C | 1 | a0008 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.987A>G | p.Ile329Met | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/13 | 1054/8698 | 987/2220 | 329/739 | chr3 | 57101356 | |||
chr3:57102557 | C | T | 1 | a0003 | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
missense_variant | MODERATE | c.901G>A | p.Val301Met | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/13 | 968/8698 | 901/2220 | 301/739 | chr3 | 57102557 | |||
chr3:57102580 | G | A | 1 | a0006 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.878C>T | p.Pro293Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/13 | 945/8698 | 878/2220 | 293/739 | chr3 | 57102580 | |||
chr3:57104391 | G | A | 6 | a0001 a0004 a0005 others(3): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
missense_variant | MODERATE | c.764C>T | p.Thr255Met | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/13 | 831/8698 | 764/2220 | 255/739 | chr3 | 57104391 | |||
chr3:57110263 | G | A | 1 | a0010 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.359C>T | p.Ser120Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/13 | 426/8698 | 359/2220 | 120/739 | chr3 | 57110263 | |||
chr3:57165283 | C | A | 1 | a0007 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.4G>T | p.Ala2Ser | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/13 | 71/8698 | 4/2220 | 2/739 | chr3 | 57165283 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57096486 | G | A | 1 | a0002c0015 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.2127C>T | p.Ala709Ala | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2194/8698 | 2127/2220 | 709/739 | chr3 | 57096486 | |||
chr3:57097879 | A | G | 1 | a0001c0013 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1824T>C | p.Ala608Ala | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1891/8698 | 1824/2220 | 608/739 | chr3 | 57097879 | |||
chr3:57098047 | A | G | 1 | a0003c0010 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1656T>C | p.Phe552Phe | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1723/8698 | 1656/2220 | 552/739 | chr3 | 57098047 | |||
chr3:57098119 | G | C | 1 | a0001c0006 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
synonymous_variant | LOW | c.1584C>G | p.Gly528Gly | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1651/8698 | 1584/2220 | 528/739 | chr3 | 57098119 | |||
chr3:57098158 | G | A | 1 | a0002c0007 | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.1545C>T | p.Asp515Asp | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1612/8698 | 1545/2220 | 515/739 | chr3 | 57098158 | |||
chr3:57098172 | A | G | 13 | a0001c0001 a0001c0006 a0001c0013 others(10): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
synonymous_variant | LOW | c.1531T>C | p.Leu511Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1598/8698 | 1531/2220 | 511/739 | chr3 | 57098172 | |||
chr3:57098320 | G | A | 1 | a0003c0011 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1383C>T | p.Leu461Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1450/8698 | 1383/2220 | 461/739 | chr3 | 57098320 | |||
chr3:57105944 | A | G | 14 | a0001c0001 a0001c0006 a0001c0013 others(11): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
synonymous_variant | LOW | c.660T>C | p.His220His | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/13 | 727/8698 | 660/2220 | 220/739 | chr3 | 57105944 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57090092 | C | A | 1 | a0001c0001t0045 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6301G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6301 | chr3 | 57090092 | ||||||
chr3:57090168 | C | G | 1 | a0002c0004t0019 | 2 | HG02922.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6225G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6225 | chr3 | 57090168 | ||||||
chr3:57090245 | C | T | 1 | a0001c0001t0039 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6148G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6148 | chr3 | 57090245 | ||||||
chr3:57090333 | A | G | 1 | a0002c0003t0012 | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6060T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6060 | chr3 | 57090333 | ||||||
chr3:57090427 | C | A | 1 | a0001c0006t0011 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5966G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5966 | chr3 | 57090427 | ||||||
chr3:57090466 | C | T | 1 | a0003c0002t0017 | 2 | HG03927.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5927G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5927 | chr3 | 57090466 | ||||||
chr3:57090490 | C | T | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(25): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*5903G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5903 | chr3 | 57090490 | ||||||
chr3:57090531 | G | A | 2 | a0001c0001t0046 a0002c0003t0012 |
6 | HG01255.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5862C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5862 | chr3 | 57090531 | ||||||
chr3:57090563 | G | A | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(25): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*5830C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5830 | chr3 | 57090563 | ||||||
chr3:57090564 | C | G | 1 | a0003c0010t0041 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5829 | chr3 | 57090564 | ||||||
chr3:57090613 | C | T | 1 | a0001c0001t0034 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5780G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5780 | chr3 | 57090613 | ||||||
chr3:57090791 | G | C | 1 | a0001c0006t0011 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5602C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5602 | chr3 | 57090791 | ||||||
chr3:57090848 | T | C | 1 | a0001c0001t0036 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5545A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5545 | chr3 | 57090848 | ||||||
chr3:57091040 | G | T | 3 | a0002c0004t0019 a0002c0004t0049 a0002c0004t0051 |
4 | HG02109.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5353C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5353 | chr3 | 57091040 | ||||||
chr3:57091073 | A | C | 8 | a0001c0001t0037 a0002c0004t0057 a0003c0002t0001 others(5): Show |
92 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*5320T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5320 | chr3 | 57091073 | ||||||
chr3:57091174 | T | G | 14 | a0001c0001t0037 a0002c0004t0008 a0002c0004t0016 others(11): Show |
107 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*5219A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5219 | chr3 | 57091174 | ||||||
chr3:57091178 | A | G | 1 | a0001c0006t0011 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5215T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5215 | chr3 | 57091178 | ||||||
chr3:57091252 | G | A | 2 | a0002c0004t0019 a0002c0004t0051 |
3 | HG02109.hp2 HG02922.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5141C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5141 | chr3 | 57091252 | ||||||
chr3:57091352 | C | T | 60 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(57): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*5041G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5041 | chr3 | 57091352 | ||||||
chr3:57091368 | A | G | 1 | a0002c0003t0022 | 2 | HG02622.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5025T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5025 | chr3 | 57091368 | ||||||
chr3:57091371 | GA | G | 2 | a0002c0003t0014 a0002c0003t0053 |
5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5021delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5021 | chr3 | 57091371 | ||||||
chr3:57091396 | G | A | 14 | a0001c0001t0037 a0002c0004t0008 a0002c0004t0016 others(11): Show |
107 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*4997C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4997 | chr3 | 57091396 | ||||||
chr3:57091402 | G | A | 1 | a0001c0001t0038 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4991C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4991 | chr3 | 57091402 | ||||||
chr3:57091493 | G | A | 2 | a0002c0003t0022 a0002c0003t0055 |
3 | HG02622.hp1 HG02630.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4900C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4900 | chr3 | 57091493 | ||||||
chr3:57091699 | T | A | 17 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0018 others(14): Show |
72 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4694A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4694 | chr3 | 57091699 | ||||||
chr3:57091836 | A | G | 6 | a0003c0002t0001 a0003c0002t0015 a0003c0002t0017 others(3): Show |
90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4557T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4557 | chr3 | 57091836 | ||||||
chr3:57092029 | C | T | 1 | a0001c0001t0044 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4364G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4364 | chr3 | 57092029 | ||||||
chr3:57092117 | C | T | 1 | a0002c0003t0053 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4276G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4276 | chr3 | 57092117 | ||||||
chr3:57092255 | C | A | 1 | a0001c0001t0047 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4138G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4138 | chr3 | 57092255 | ||||||
chr3:57092315 | G | A | 1 | a0002c0004t0016 | 3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4078C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4078 | chr3 | 57092315 | ||||||
chr3:57092333 | A | T | 2 | a0002c0004t0048 a0005c0005t0010 |
7 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4060T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4060 | chr3 | 57092333 | ||||||
chr3:57092398 | C | T | 1 | a0002c0004t0008 | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3995G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3995 | chr3 | 57092398 | ||||||
chr3:57092462 | G | GC | 6 | a0002c0003t0032 a0003c0002t0001 a0003c0002t0017 others(3): Show |
88 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*3930dupG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3930 | chr3 | 57092462 | ||||||
chr3:57092588 | CA | C | 39 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(36): Show |
157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*3804delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3804 | chr3 | 57092588 | ||||||
chr3:57092753 | G | T | 1 | a0001c0001t0033 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3640C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3640 | chr3 | 57092753 | ||||||
chr3:57092822 | G | A | 1 | a0001c0001t0042 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3571C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3571 | chr3 | 57092822 | ||||||
chr3:57093053 | C | T | 1 | a0001c0001t0043 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3340G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3340 | chr3 | 57093053 | ||||||
chr3:57093220 | G | A | 3 | a0002c0003t0014 a0002c0003t0053 a0002c0003t0054 |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3173C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3173 | chr3 | 57093220 | ||||||
chr3:57093273 | T | C | 1 | a0001c0001t0027 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3120 | chr3 | 57093273 | ||||||
chr3:57093326 | T | C | 2 | a0001c0001t0018 a0006c0014t0018 |
2 | HG02486.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3067A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3067 | chr3 | 57093326 | ||||||
chr3:57093428 | A | T | 7 | a0002c0004t0016 a0002c0004t0019 a0002c0004t0048 others(4): Show |
10 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2965T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2965 | chr3 | 57093428 | ||||||
chr3:57093463 | G | A | 2 | a0001c0001t0018 a0006c0014t0018 |
2 | HG02486.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2930C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2930 | chr3 | 57093463 | ||||||
chr3:57093541 | A | G | 1 | a0002c0003t0030 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2852T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2852 | chr3 | 57093541 | ||||||
chr3:57093963 | G | A | 51 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(48): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*2430C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2430 | chr3 | 57093963 | ||||||
chr3:57094183 | G | A | 9 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0028 others(6): Show |
37 | HG00280.hp2 HG01081.hp2 HG01168.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2210C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2210 | chr3 | 57094183 | ||||||
chr3:57094186 | T | C | 8 | a0002c0004t0008 a0002c0004t0016 a0002c0004t0019 others(5): Show |
17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2207A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2207 | chr3 | 57094186 | ||||||
chr3:57094231 | T | G | 1 | a0001c0001t0052 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2162A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2162 | chr3 | 57094231 | ||||||
chr3:57094273 | C | T | 1 | a0001c0001t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2120G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2120 | chr3 | 57094273 | ||||||
chr3:57094385 | G | A | 1 | a0002c0004t0057 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2008C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2008 | chr3 | 57094385 | ||||||
chr3:57094482 | T | C | 3 | a0002c0003t0014 a0002c0003t0053 a0002c0003t0054 |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1911A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1911 | chr3 | 57094482 | ||||||
chr3:57094652 | G | A | 1 | a0002c0003t0012 | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1741C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1741 | chr3 | 57094652 | ||||||
chr3:57094751 | G | A | 3 | a0002c0003t0014 a0002c0003t0053 a0002c0003t0054 |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1642C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1642 | chr3 | 57094751 | ||||||
chr3:57094813 | T | C | 1 | a0001c0001t0020 | 2 | HG01106.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1580A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1580 | chr3 | 57094813 | ||||||
chr3:57094833 | C | T | 1 | a0001c0001t0028 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1560G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1560 | chr3 | 57094833 | ||||||
chr3:57094974 | G | T | 1 | a0001c0001t0027 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1419C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1419 | chr3 | 57094974 | ||||||
chr3:57095121 | C | A | 4 | a0002c0003t0013 a0002c0003t0021 a0002c0003t0022 others(1): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1272G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1272 | chr3 | 57095121 | ||||||
chr3:57095142 | C | T | 1 | a0001c0001t0026 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1251 | chr3 | 57095142 | ||||||
chr3:57095681 | T | A | 1 | a0001c0001t0056 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 712 | chr3 | 57095681 | ||||||
chr3:57095810 | T | C | 1 | a0002c0004t0008 | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*583A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 583 | chr3 | 57095810 | ||||||
chr3:57096238 | T | C | 1 | a0002c0004t0057 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 155 | chr3 | 57096238 | ||||||
chr3:57165312 | G | A | 1 | a0003c0002t0023 | 2 | NA18993.hp1 NA19002.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/13 | chr3 | 57165312 | |||||||
chr3:57165322 | C | A | 2 | a0001c0001t0024 a0001c0001t0025 |
4 | HG01257.hp2 HG02145.hp1 HG03710.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/13 | 36 | chr3 | 57165322 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57096615 | TA | T | 97 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(94): Show |
98 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.2108-111delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096615 | |||||||
chr3:57096631 | C | T | 9 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2108-126G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096631 | |||||||
chr3:57096633 | C | T | 5 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(2): Show |
5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108-128G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096633 | |||||||
chr3:57096717 | T | A | 1 | a0002c0003t0031g0288 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2108-212A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096717 | |||||||
chr3:57096860 | A | C | 4 | a0002c0004t0008g0215 a0002c0004t0008g0264 a0002c0004t0008g0298 others(1): Show |
4 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108-355T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096860 | |||||||
chr3:57096953 | T | G | 89 | a0003c0002t0001g0016 a0003c0002t0001g0018 a0003c0002t0001g0024 others(86): Show |
90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.2108-448A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096953 | |||||||
chr3:57097004 | C | CA | 11 | a0001c0001t0003g0234 a0001c0001t0018g0331 a0002c0003t0002g0072 others(8): Show |
11 | HG00673.hp1 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2108-500dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097004 | |||||||
chr3:57097004 | CA | C | 104 | a0001c0001t0003g0286 a0001c0001t0004g0226 a0001c0001t0037g0041 others(101): Show |
105 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.2108-500delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097004 | |||||||
chr3:57097083 | G | A | 17 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(14): Show |
17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.2107+513C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097083 | |||||||
chr3:57097193 | A | G | 1 | a0001c0001t0042g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2107+403T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097193 | |||||||
chr3:57097365 | C | A | 1 | a0002c0003t0012g0156 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2107+231G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097365 | |||||||
chr3:57097372 | A | G | 1 | a0002c0003t0012g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2107+224T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097372 | |||||||
chr3:57097501 | A | C | 183 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2107+95T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097501 | |||||||
chr3:57098666 | A | G | 1 | a0002c0003t0021g0340 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1165-128T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57098666 | |||||||
chr3:57098667 | T | C | 2 | a0001c0001t0004g0112 a0001c0001t0040g0182 |
2 | HG01978.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1165-129A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57098667 | |||||||
chr3:57098712 | C | G | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1165-174G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57098712 | |||||||
chr3:57099110 | G | A | 150 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(147): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1165-572C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099110 | |||||||
chr3:57099117 | T | C | 1 | a0002c0003t0031g0288 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1165-579A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099117 | |||||||
chr3:57099295 | C | G | 1 | a0003c0002t0001g0055 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1165-757G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099295 | |||||||
chr3:57099661 | A | G | 5 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165-1123T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099661 | |||||||
chr3:57099749 | A | C | 1 | a0003c0002t0001g0296 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1165-1211T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099749 | |||||||
chr3:57099922 | C | T | 5 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0310 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164+1257G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099922 | |||||||
chr3:57100087 | A | G | 241 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(238): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1164+1092T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100087 | |||||||
chr3:57100114 | G | C | 3 | a0003c0002t0001g0027 a0003c0002t0001g0052 a0003c0002t0001g0089 |
3 | HG01934.hp2 HG02293.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1164+1065C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100114 | |||||||
chr3:57100202 | T | C | 261 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(258): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1164+977A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100202 | |||||||
chr3:57100218 | C | T | 142 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(139): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1164+961G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100218 | |||||||
chr3:57100362 | C | T | 1 | a0003c0002t0001g0070 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+817G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100362 | |||||||
chr3:57100768 | G | A | 1 | a0001c0001t0007g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1164+411C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100768 | |||||||
chr3:57100858 | C | T | 1 | a0005c0005t0010g0332 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1164+321G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100858 | |||||||
chr3:57100940 | CAAAGCTT others(1): Show |
C | 5 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(2): Show |
5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164+231_1164+238d others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100940 | |||||||
chr3:57101034 | G | A | 1 | a0003c0002t0001g0049 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1164+145C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57101034 | |||||||
chr3:57101073 | G | A | 1 | a0003c0002t0001g0147 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1164+106C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57101073 | |||||||
chr3:57101379 | A | T | 1 | a0001c0001t0003g0235 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.980-16T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101379 | |||||||
chr3:57101432 | A | G | 2 | a0001c0001t0018g0331 a0006c0014t0018g0330 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.980-69T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101432 | |||||||
chr3:57101488 | C | T | 1 | a0001c0001t0034g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-125G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101488 | |||||||
chr3:57101490 | C | G | 240 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(237): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.980-127G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101490 | |||||||
chr3:57101633 | G | A | 3 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 |
3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.980-270C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101633 | |||||||
chr3:57101707 | C | G | 1 | a0001c0001t0027g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.980-344G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101707 | |||||||
chr3:57101723 | T | A | 256 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(253): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.980-360A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101723 | |||||||
chr3:57101907 | A | G | 1 | a0003c0002t0001g0143 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.980-544T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101907 | |||||||
chr3:57101952 | C | A | 283 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.979+527G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101952 | |||||||
chr3:57102013 | AT | A | 256 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(253): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.979+465delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102013 | |||||||
chr3:57102015 | G | C | 256 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(253): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.979+464C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102015 | |||||||
chr3:57102016 | A | T | 256 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(253): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.979+463T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102016 | |||||||
chr3:57102017 | G | T | 256 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(253): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.979+462C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102017 | |||||||
chr3:57102018 | A | T | 256 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(253): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.979+461T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102018 | |||||||
chr3:57102114 | T | C | 1 | a0002c0004t0049g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.979+365A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102114 | |||||||
chr3:57102115 | A | T | 7 | a0002c0003t0022g0097 a0002c0003t0022g0216 a0002c0003t0055g0009 others(4): Show |
7 | HG01496.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+364T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102115 | |||||||
chr3:57102278 | G | A | 6 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+201C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102278 | |||||||
chr3:57102670 | A | G | 1 | a0001c0001t0027g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.869-81T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57102670 | |||||||
chr3:57102685 | G | C | 6 | a0005c0005t0010g0061 a0005c0005t0010g0062 a0005c0005t0010g0090 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-96C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57102685 | |||||||
chr3:57102785 | T | C | 5 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-196A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57102785 | |||||||
chr3:57103062 | A | G | 257 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(254): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.868+29T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57103062 | |||||||
chr3:57103204 | GA | G | 89 | a0003c0002t0001g0016 a0003c0002t0001g0018 a0003c0002t0001g0024 others(86): Show |
90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.814-60delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103204 | |||||||
chr3:57103265 | G | A | 1 | a0002c0003t0002g0217 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.814-120C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103265 | |||||||
chr3:57103353 | C | T | 1 | a0003c0002t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.814-208G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103353 | |||||||
chr3:57103433 | C | A | 142 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(139): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.814-288G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103433 | |||||||
chr3:57103495 | G | A | 6 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0183 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-350C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103495 | |||||||
chr3:57103508 | G | GT | 4 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0323 others(1): Show |
4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-364dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103508 | |||||||
chr3:57103568 | A | C | 89 | a0003c0002t0001g0016 a0003c0002t0001g0018 a0003c0002t0001g0024 others(86): Show |
90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.814-423T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103568 | |||||||
chr3:57103744 | A | G | 257 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(254): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.813+598T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103744 | |||||||
chr3:57103783 | C | G | 34 | a0001c0001t0005g0001 a0001c0001t0005g0017 a0001c0001t0005g0033 others(31): Show |
37 | HG00280.hp2 HG01081.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.813+559G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103783 | |||||||
chr3:57103864 | CCAGCT | C | 4 | a0002c0004t0019g0006 a0002c0004t0019g0007 a0002c0004t0048g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+473_813+477del others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103864 | |||||||
chr3:57103870 | A | T | 4 | a0002c0004t0019g0006 a0002c0004t0019g0007 a0002c0004t0048g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+472T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103870 | |||||||
chr3:57103871 | A | G | 4 | a0002c0004t0019g0006 a0002c0004t0019g0007 a0002c0004t0048g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+471T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103871 | |||||||
chr3:57103939 | T | C | 9 | a0001c0001t0004g0226 a0001c0001t0004g0315 a0001c0001t0038g0035 others(6): Show |
9 | HG02145.hp2 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+403A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103939 | |||||||
chr3:57104069 | A | G | 1 | a0003c0002t0001g0027 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.813+273T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57104069 | |||||||
chr3:57104200 | T | A | 89 | a0003c0002t0001g0016 a0003c0002t0001g0018 a0003c0002t0001g0024 others(86): Show |
90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.813+142A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57104200 | |||||||
chr3:57104288 | T | C | 2 | a0001c0001t0034g0100 a0001c0001t0042g0019 |
2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.813+54A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57104288 | |||||||
chr3:57104695 | C | T | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.748-288G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104695 | |||||||
chr3:57104852 | C | T | 1 | a0002c0003t0013g0326 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.748-445G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104852 | |||||||
chr3:57104947 | G | A | 8 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(5): Show |
8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-540C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104947 | |||||||
chr3:57104995 | T | C | 6 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0183 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-588A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104995 | |||||||
chr3:57105180 | T | C | 1 | a0002c0003t0002g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.747+677A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105180 | |||||||
chr3:57105303 | C | T | 7 | a0001c0001t0004g0004 a0001c0001t0004g0190 a0001c0001t0004g0191 others(4): Show |
8 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.747+554G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105303 | |||||||
chr3:57105397 | T | C | 286 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(283): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.747+460A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105397 | |||||||
chr3:57105480 | C | T | 17 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(14): Show |
17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.747+377G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105480 | |||||||
chr3:57105494 | A | G | 1 | a0003c0002t0001g0137 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.747+363T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105494 | |||||||
chr3:57105536 | C | CA | 8 | a0003c0002t0001g0018 a0003c0002t0001g0024 a0003c0002t0001g0027 others(5): Show |
8 | HG00639.hp2 NA18948.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.747+320dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | |||||||
chr3:57105536 | C | CAA | 60 | a0002c0003t0032g0303 a0003c0002t0001g0025 a0003c0002t0001g0026 others(57): Show |
61 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.747+319_747+320dup others(2): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | |||||||
chr3:57105536 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0289 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.747+309_747+320dup others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | |||||||
chr3:57105536 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0003g0186 a0001c0001t0003g0291 a0001c0001t0003g0293 |
3 | HG01496.hp1 HG02083.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.747+308_747+320dup others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | |||||||
chr3:57105536 | C | CAAAAAAA others(7): Show |
30 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(27): Show |
30 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.747+307_747+320dup others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | |||||||
chr3:57105536 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0003g0253 a0001c0001t0003g0284 |
2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.747+306_747+320dup others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | |||||||
chr3:57105548 | AAAAAAT | A | 9 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.747+303_747+308del others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105548 | |||||||
chr3:57105552 | A | AAAAAAAA others(40): Show |
1 | a0002c0003t0012g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(47): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(42): Show |
1 | a0002c0003t0012g0221 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(49): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(8): Show |
18 | a0001c0001t0004g0045 a0001c0001t0004g0112 a0001c0001t0004g0191 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(10): Show |
1 | a0005c0005t0010g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(17): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(7): Show |
20 | a0001c0001t0003g0256 a0001c0001t0003g0334 a0001c0001t0004g0004 others(17): Show |
21 | HG01071.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0034g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(15): Show |
4 | a0002c0003t0013g0078 a0002c0003t0013g0325 a0002c0003t0021g0279 others(1): Show |
4 | HG01934.hp1 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(33): Show |
1 | a0002c0003t0012g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(40): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(6): Show |
11 | a0001c0001t0004g0184 a0001c0001t0004g0317 a0001c0001t0004g0318 others(8): Show |
11 | HG01069.hp2 HG01243.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(8): Show |
12 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0240 others(9): Show |
12 | HG00738.hp2 HG01106.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(7): Show |
14 | a0001c0001t0003g0111 a0001c0001t0003g0258 a0001c0001t0003g0259 others(11): Show |
16 | HG01168.hp1 HG01884.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0004g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(6): Show |
6 | a0001c0001t0005g0017 a0001c0001t0005g0033 a0001c0001t0005g0165 others(3): Show |
6 | HG02698.hp2 HG02735.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(8): Show |
5 | a0001c0001t0007g0152 a0001c0001t0043g0154 a0001c0001t0052g0299 others(2): Show |
5 | HG01243.hp1 HG01978.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(14): Show |
2 | a0002c0003t0013g0063 a0002c0003t0013g0324 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.747+304_747+305ins others(21): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(7): Show |
7 | a0001c0001t0005g0161 a0001c0001t0005g0196 a0001c0001t0005g0197 others(4): Show |
7 | HG01081.hp2 HG01358.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(15): Show |
1 | a0002c0003t0013g0326 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(37): Show |
1 | a0002c0003t0012g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(44): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(6): Show |
4 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0323 others(1): Show |
4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(8): Show |
3 | a0001c0001t0007g0003 a0001c0001t0007g0032 a0001c0001t0007g0151 |
4 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(28): Show |
1 | a0002c0007t0009g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(5): Show |
1 | a0002c0003t0053g0171 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAA others(33): Show |
1 | a0002c0003t0012g0156 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(40): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAT others(6): Show |
1 | a0002c0003t0054g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAT others(28): Show |
1 | a0002c0007t0009g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAAAAT others(32): Show |
1 | a0002c0007t0009g0312 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(39): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAATAT others(6): Show |
1 | a0002c0003t0014g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAAATAT others(8): Show |
1 | a0002c0007t0009g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAATATA others(11): Show |
2 | a0002c0004t0008g0264 a0002c0004t0008g0298 |
2 | HG00099.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.747+304_747+305ins others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAATATA others(13): Show |
1 | a0002c0004t0008g0322 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAATATA others(27): Show |
1 | a0002c0007t0009g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(34): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAATATA others(33): Show |
1 | a0002c0003t0022g0216 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(40): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAAATATA others(35): Show |
1 | a0002c0007t0009g0311 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(42): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAATATAT others(4): Show |
1 | a0001c0006t0011g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(11): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AAT | 11 | a0003c0002t0001g0056 a0003c0002t0001g0057 a0003c0002t0001g0070 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.747+303_747+304dup others(2): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AATATATA others(3): Show |
1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.747+295_747+304dup others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AATATATA others(11): Show |
1 | a0002c0004t0008g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.747+287_747+304dup others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AATATATA others(31): Show |
1 | a0002c0003t0055g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(38): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | AT | 4 | a0002c0003t0002g0093 a0002c0003t0002g0204 a0003c0002t0001g0058 others(1): Show |
4 | HG01891.hp1 HG06807.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(1): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | ATATATAT others(2): Show |
3 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 |
3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.747+304_747+305ins others(9): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | ATATATAT others(28): Show |
1 | a0002c0003t0022g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105552 | A | T | 12 | a0002c0003t0002g0064 a0002c0003t0002g0092 a0002c0003t0002g0155 others(9): Show |
12 | HG01169.hp2 HG01928.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.747+305T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | |||||||
chr3:57105554 | T | A | 2 | a0001c0001t0003g0228 a0001c0001t0003g0229 |
2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.747+303A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105554 | |||||||
chr3:57105581 | A | C | 1 | a0003c0002t0001g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.747+276T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105581 | |||||||
chr3:57105701 | T | C | 1 | a0003c0002t0001g0136 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.747+156A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105701 | |||||||
chr3:57105805 | G | A | 239 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(236): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.747+52C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105805 | |||||||
chr3:57106057 | C | G | 1 | a0001c0001t0003g0187 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.596-49G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 6/12 | chr3 | 57106057 | |||||||
chr3:57106080 | G | A | 239 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(236): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.595+30C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 6/12 | chr3 | 57106080 | |||||||
chr3:57106167 | TA | T | 3 | a0003c0002t0001g0219 a0003c0002t0015g0220 a0003c0002t0015g0290 |
3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.551-14delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106167 | |||||||
chr3:57106339 | T | C | 1 | a0001c0001t0003g0289 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.551-185A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106339 | |||||||
chr3:57106415 | G | C | 7 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-261C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106415 | |||||||
chr3:57106420 | G | A | 8 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(5): Show |
8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.551-266C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106420 | |||||||
chr3:57106501 | T | C | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.551-347A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106501 | |||||||
chr3:57106766 | A | G | 89 | a0003c0002t0001g0016 a0003c0002t0001g0018 a0003c0002t0001g0024 others(86): Show |
90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.551-612T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106766 | |||||||
chr3:57106805 | T | A | 9 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.551-651A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106805 | |||||||
chr3:57106920 | T | G | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.551-766A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106920 | |||||||
chr3:57106935 | C | T | 3 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0229 |
3 | HG00099.hp2 HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.551-781G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106935 | |||||||
chr3:57106977 | G | A | 1 | a0001c0001t0004g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.551-823C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106977 | |||||||
chr3:57107035 | T | C | 1 | a0001c0001t0038g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.551-881A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107035 | |||||||
chr3:57107100 | C | T | 1 | a0001c0001t0026g0267 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.551-946G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107100 | |||||||
chr3:57107101 | G | A | 1 | a0002c0003t0002g0064 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.551-947C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107101 | |||||||
chr3:57107105 | G | A | 1 | a0001c0001t0052g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.551-951C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107105 | |||||||
chr3:57107149 | C | T | 5 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.551-995G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107149 | |||||||
chr3:57107156 | A | T | 1 | a0002c0003t0002g0040 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.551-1002T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107156 | |||||||
chr3:57107305 | G | A | 7 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-1151C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107305 | |||||||
chr3:57107327 | C | T | 7 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0107 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-1173G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107327 | |||||||
chr3:57107328 | G | A | 6 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-1174C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107328 | |||||||
chr3:57107355 | G | C | 1 | a0001c0001t0003g0289 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.551-1201C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107355 | |||||||
chr3:57107379 | G | GA | 9 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG03195.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.551-1226dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107379 | |||||||
chr3:57107379 | G | GAA | 87 | a0002c0003t0032g0303 a0003c0002t0001g0016 a0003c0002t0001g0018 others(84): Show |
88 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.551-1227_551-1226d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107379 | |||||||
chr3:57107385 | A | AG | 158 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(155): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.551-1232_551-1231i others(3): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107385 | |||||||
chr3:57107386 | A | G | 2 | a0005c0005t0010g0090 a0005c0005t0010g0091 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.551-1232T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107386 | |||||||
chr3:57107462 | A | C | 159 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.551-1308T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107462 | |||||||
chr3:57107556 | C | T | 10 | a0002c0003t0013g0063 a0002c0003t0013g0078 a0002c0003t0013g0324 others(7): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.551-1402G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107556 | |||||||
chr3:57107807 | C | T | 1 | a0002c0003t0002g0302 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.551-1653G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107807 | |||||||
chr3:57107947 | T | C | 1 | a0002c0003t0002g0098 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.550+1590A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107947 | |||||||
chr3:57108066 | T | C | 63 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(60): Show |
63 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.550+1471A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108066 | |||||||
chr3:57108148 | C | T | 5 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.550+1389G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108148 | |||||||
chr3:57108305 | C | T | 1 | a0001c0001t0004g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550+1232G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108305 | |||||||
chr3:57108317 | T | G | 258 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(255): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.550+1220A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108317 | |||||||
chr3:57108509 | C | CT | 155 | a0001c0001t0003g0015 a0001c0001t0003g0104 a0001c0001t0003g0107 others(152): Show |
159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.550+1027dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | |||||||
chr3:57108509 | C | CTT | 40 | a0001c0001t0003g0043 a0001c0001t0003g0227 a0001c0001t0003g0256 others(37): Show |
40 | HG00544.hp2 HG00609.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.550+1026_550+1027d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | |||||||
chr3:57108509 | C | CTTT | 8 | a0001c0001t0004g0184 a0002c0003t0022g0097 a0002c0003t0055g0009 others(5): Show |
8 | HG01069.hp1 HG01169.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+1025_550+1027d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | |||||||
chr3:57108509 | C | CTTTT | 80 | a0002c0003t0013g0325 a0002c0003t0013g0326 a0002c0003t0014g0170 others(77): Show |
81 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.550+1024_550+1027d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | |||||||
chr3:57108509 | C | CTTTTT | 21 | a0002c0003t0014g0172 a0002c0003t0014g0323 a0002c0004t0008g0215 others(18): Show |
21 | HG00099.hp1 HG01071.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.550+1023_550+1027d others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | |||||||
chr3:57108509 | C | CTTTTTT | 9 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0320 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+1022_550+1027d others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | |||||||
chr3:57108576 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550+961G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108576 | |||||||
chr3:57108631 | G | A | 142 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(139): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.550+906C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108631 | |||||||
chr3:57108661 | G | A | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.550+876C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108661 | |||||||
chr3:57108670 | G | T | 1 | a0001c0001t0027g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.550+867C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108670 | |||||||
chr3:57108734 | T | G | 2 | a0001c0001t0018g0331 a0006c0014t0018g0330 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.550+803A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108734 | |||||||
chr3:57108741 | A | C | 3 | a0001c0001t0004g0231 a0001c0001t0004g0232 a0001c0001t0004g0241 |
3 | HG02040.hp2 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.550+796T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108741 | |||||||
chr3:57108768 | G | A | 1 | a0002c0003t0002g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.550+769C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108768 | |||||||
chr3:57108807 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550+730G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108807 | |||||||
chr3:57108943 | GGTAATGC others(23): Show |
G | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.550+564_550+593del others(30): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108943 | |||||||
chr3:57109166 | T | A | 1 | a0002c0003t0002g0262 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.550+371A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109166 | |||||||
chr3:57109220 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.550+317G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109220 | |||||||
chr3:57109222 | C | T | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.550+315G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109222 | |||||||
chr3:57109348 | T | C | 258 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(255): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.550+189A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109348 | |||||||
chr3:57109822 | G | C | 8 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(5): Show |
8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-165C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109822 | |||||||
chr3:57109895 | C | T | 3 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 |
3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.430-238G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109895 | |||||||
chr3:57109914 | C | T | 94 | a0001c0001t0003g0236 a0001c0001t0004g0184 a0001c0001t0004g0317 others(91): Show |
95 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.430-257G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109914 | |||||||
chr3:57109931 | T | C | 17 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(14): Show |
17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.429+262A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109931 | |||||||
chr3:57109967 | A | G | 142 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(139): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.429+226T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109967 | |||||||
chr3:57109986 | G | C | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.429+207C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109986 | |||||||
chr3:57110000 | C | T | 9 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+193G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57110000 | |||||||
chr3:57110034 | TG | T | 10 | a0002c0003t0013g0063 a0002c0003t0013g0078 a0002c0003t0013g0324 others(7): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+158delC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57110034 | |||||||
chr3:57110327 | T | A | 1 | a0002c0003t0002g0335 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.311-16A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110327 | |||||||
chr3:57110628 | A | G | 3 | a0003c0002t0001g0144 a0003c0002t0001g0146 a0003c0002t0015g0145 |
3 | HG02896.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.311-317T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110628 | |||||||
chr3:57110642 | T | C | 10 | a0002c0003t0013g0063 a0002c0003t0013g0078 a0002c0003t0013g0324 others(7): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.311-331A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110642 | |||||||
chr3:57110678 | A | G | 6 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-367T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110678 | |||||||
chr3:57110771 | T | C | 17 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(14): Show |
17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.311-460A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110771 | |||||||
chr3:57110888 | A | G | 1 | a0001c0001t0003g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.311-577T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110888 | |||||||
chr3:57110944 | G | A | 2 | a0005c0005t0010g0061 a0005c0005t0010g0062 |
2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.311-633C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110944 | |||||||
chr3:57110961 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.311-650C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110961 | |||||||
chr3:57111132 | G | A | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.311-821C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111132 | |||||||
chr3:57111244 | A | G | 1 | a0001c0001t0004g0207 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.311-933T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111244 | |||||||
chr3:57111279 | G | C | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.311-968C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111279 | |||||||
chr3:57111515 | G | A | 10 | a0002c0003t0013g0063 a0002c0003t0013g0078 a0002c0003t0013g0324 others(7): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.311-1204C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111515 | |||||||
chr3:57111570 | A | G | 2 | a0002c0003t0002g0304 a0002c0003t0002g0306 |
2 | NA18982.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.311-1259T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111570 | |||||||
chr3:57111698 | C | T | 84 | a0003c0002t0001g0016 a0003c0002t0001g0025 a0003c0002t0001g0026 others(81): Show |
85 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.311-1387G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111698 | |||||||
chr3:57111709 | G | A | 34 | a0001c0001t0005g0001 a0001c0001t0005g0017 a0001c0001t0005g0033 others(31): Show |
37 | HG00280.hp2 HG01081.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-1398C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111709 | |||||||
chr3:57111742 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.311-1431C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111742 | |||||||
chr3:57111802 | C | CA | 143 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(140): Show |
147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.311-1492dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111802 | |||||||
chr3:57111864 | A | C | 4 | a0001c0001t0004g0184 a0001c0001t0004g0317 a0001c0001t0004g0318 others(1): Show |
4 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-1553T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111864 | |||||||
chr3:57111893 | C | T | 5 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(2): Show |
5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-1582G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111893 | |||||||
chr3:57111983 | G | GA | 7 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(4): Show |
7 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-1673dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111983 | |||||||
chr3:57111987 | A | G | 6 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0183 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-1676T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111987 | |||||||
chr3:57112098 | G | A | 1 | a0001c0001t0007g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.311-1787C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112098 | |||||||
chr3:57112470 | T | C | 6 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0183 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-2159A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112470 | |||||||
chr3:57112509 | C | T | 10 | a0002c0003t0013g0063 a0002c0003t0013g0078 a0002c0003t0013g0324 others(7): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.310+2183G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112509 | |||||||
chr3:57112620 | A | G | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+2072T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112620 | |||||||
chr3:57112659 | C | A | 6 | a0001c0001t0006g0099 a0001c0001t0006g0103 a0001c0001t0006g0105 others(3): Show |
6 | HG02451.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+2033G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112659 | |||||||
chr3:57112701 | G | T | 7 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+1991C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112701 | |||||||
chr3:57112702 | TTAAAACC others(4): Show |
T | 7 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+1979_310+1989d others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112702 | |||||||
chr3:57112743 | A | G | 1 | a0002c0004t0008g0320 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.310+1949T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112743 | |||||||
chr3:57112880 | G | A | 10 | a0002c0003t0013g0063 a0002c0003t0013g0078 a0002c0003t0013g0324 others(7): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.310+1812C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112880 | |||||||
chr3:57113011 | T | C | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+1681A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113011 | |||||||
chr3:57113101 | A | G | 285 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(282): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.310+1591T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113101 | |||||||
chr3:57113143 | T | C | 1 | a0002c0004t0008g0077 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.310+1549A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113143 | |||||||
chr3:57113171 | C | A | 6 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.310+1521G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113171 | |||||||
chr3:57113216 | T | C | 2 | a0005c0005t0010g0090 a0005c0005t0010g0091 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.310+1476A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113216 | |||||||
chr3:57113330 | T | C | 1 | a0001c0001t0038g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.310+1362A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113330 | |||||||
chr3:57113434 | A | C | 2 | a0001c0001t0003g0250 a0001c0001t0003g0261 |
2 | NA18957.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.310+1258T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113434 | |||||||
chr3:57113445 | C | G | 1 | a0002c0003t0002g0073 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.310+1247G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113445 | |||||||
chr3:57113529 | G | A | 9 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.310+1163C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113529 | |||||||
chr3:57113536 | C | T | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+1156G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113536 | |||||||
chr3:57113561 | G | A | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+1131C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113561 | |||||||
chr3:57113950 | C | T | 2 | a0003c0002t0001g0016 a0003c0002t0001g0120 |
2 | NA18956.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.310+742G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113950 | |||||||
chr3:57114065 | TC | T | 97 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(94): Show |
98 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.310+626delG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114065 | |||||||
chr3:57114150 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.310+542G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114150 | |||||||
chr3:57114183 | CA | C | 91 | a0001c0001t0003g0234 a0001c0001t0004g0226 a0001c0001t0024g0346 others(88): Show |
92 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.310+508delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114183 | |||||||
chr3:57114243 | C | T | 97 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(94): Show |
98 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.310+449G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114243 | |||||||
chr3:57114315 | C | T | 1 | a0001c0001t0003g0307 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.310+377G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114315 | |||||||
chr3:57114346 | C | T | 3 | a0003c0002t0001g0169 a0003c0002t0017g0087 a0003c0002t0017g0132 |
3 | HG01109.hp1 HG03927.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.310+346G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114346 | |||||||
chr3:57114827 | A | AG | 6 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.185-11dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57114827 | |||||||
chr3:57114882 | T | C | 1 | a0003c0002t0001g0051 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185-65A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57114882 | |||||||
chr3:57114940 | C | A | 142 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(139): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.185-123G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57114940 | |||||||
chr3:57115166 | T | G | 35 | a0001c0001t0004g0004 a0001c0001t0004g0045 a0001c0001t0004g0101 others(32): Show |
36 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.185-349A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115166 | |||||||
chr3:57115185 | T | C | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.185-368A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115185 | |||||||
chr3:57115201 | C | T | 150 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.185-384G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115201 | |||||||
chr3:57115219 | G | A | 8 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(5): Show |
8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-402C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115219 | |||||||
chr3:57115220 | T | C | 1 | a0004c0008t0006g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.185-403A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115220 | |||||||
chr3:57115287 | T | G | 98 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(95): Show |
99 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.185-470A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115287 | |||||||
chr3:57115397 | T | A | 150 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.185-580A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115397 | |||||||
chr3:57115409 | A | G | 1 | a0001c0001t0003g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.185-592T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115409 | |||||||
chr3:57115581 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185-764G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115581 | |||||||
chr3:57115631 | C | T | 150 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.185-814G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115631 | |||||||
chr3:57115699 | G | C | 5 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-882C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115699 | |||||||
chr3:57115765 | C | T | 98 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(95): Show |
99 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.185-948G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115765 | |||||||
chr3:57115896 | A | G | 1 | a0003c0002t0001g0177 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.185-1079T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115896 | |||||||
chr3:57116000 | A | G | 1 | a0001c0001t0007g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.185-1183T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116000 | |||||||
chr3:57116095 | T | A | 21 | a0001c0001t0005g0001 a0001c0001t0005g0017 a0001c0001t0005g0033 others(18): Show |
23 | HG01081.hp2 HG01168.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.185-1278A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116095 | |||||||
chr3:57116162 | T | C | 1 | a0002c0003t0014g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185-1345A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116162 | |||||||
chr3:57116244 | T | C | 4 | a0001c0001t0004g0184 a0001c0001t0004g0317 a0001c0001t0004g0318 others(1): Show |
4 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-1427A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116244 | |||||||
chr3:57116282 | C | CT | 7 | a0001c0001t0027g0167 a0002c0003t0002g0155 a0002c0003t0014g0170 others(4): Show |
7 | HG02622.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.185-1466dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116282 | |||||||
chr3:57116282 | CT | C | 251 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.185-1466delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116282 | |||||||
chr3:57116282 | CTT | C | 11 | a0001c0001t0005g0327 a0001c0001t0006g0222 a0001c0001t0007g0188 others(8): Show |
11 | HG01074.hp1 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.185-1467_185-1466d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116282 | |||||||
chr3:57116288 | T | C | 8 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(5): Show |
8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-1471A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116288 | |||||||
chr3:57116430 | T | C | 2 | a0001c0001t0018g0331 a0006c0014t0018g0330 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.185-1613A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116430 | |||||||
chr3:57116444 | C | T | 1 | a0004c0009t0003g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.185-1627G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116444 | |||||||
chr3:57116458 | AT | A | 248 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(245): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.185-1642delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116458 | |||||||
chr3:57116530 | C | A | 6 | a0002c0003t0002g0002 a0002c0003t0002g0134 a0002c0003t0002g0301 others(3): Show |
8 | NA18946.hp2 NA18950.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-1713G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116530 | |||||||
chr3:57116771 | T | C | 1 | a0003c0002t0001g0030 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.185-1954A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116771 | |||||||
chr3:57116834 | G | A | 1 | a0002c0003t0014g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185-2017C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116834 | |||||||
chr3:57116842 | G | A | 4 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0323 others(1): Show |
4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-2025C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116842 | |||||||
chr3:57116889 | T | C | 8 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(5): Show |
8 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-2072A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116889 | |||||||
chr3:57116890 | T | TA | 11 | a0002c0003t0002g0039 a0002c0003t0002g0086 a0002c0003t0002g0155 others(8): Show |
11 | HG01255.hp1 HG01891.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.185-2074dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116890 | |||||||
chr3:57116890 | TA | T | 12 | a0001c0001t0005g0161 a0002c0003t0002g0037 a0002c0003t0002g0092 others(9): Show |
12 | HG01358.hp1 HG02109.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.185-2074delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116890 | |||||||
chr3:57116890 | TAA | T | 242 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.185-2075_185-2074d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116890 | |||||||
chr3:57116939 | ATATTTTG others(11): Show |
A | 1 | a0002c0003t0002g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.185-2140_185-2123d others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116939 | |||||||
chr3:57117103 | A | C | 150 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.185-2286T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117103 | |||||||
chr3:57117106 | T | A | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185-2289A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117106 | |||||||
chr3:57117113 | A | AT | 230 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0107 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.185-2297dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117113 | |||||||
chr3:57117113 | A | ATT | 18 | a0001c0001t0003g0104 a0001c0001t0004g0240 a0001c0001t0005g0199 others(15): Show |
18 | HG00558.hp2 HG00639.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-2298_185-2297d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117113 | |||||||
chr3:57117199 | C | T | 1 | a0002c0003t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.185-2382G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117199 | |||||||
chr3:57117234 | C | T | 3 | a0003c0002t0001g0144 a0003c0002t0001g0146 a0003c0002t0015g0145 |
3 | HG02896.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.185-2417G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117234 | |||||||
chr3:57117339 | C | G | 10 | a0002c0003t0013g0063 a0002c0003t0013g0078 a0002c0003t0013g0324 others(7): Show |
10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.185-2522G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117339 | |||||||
chr3:57117534 | A | T | 1 | a0001c0001t0006g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.185-2717T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117534 | |||||||
chr3:57117768 | C | G | 6 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0183 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+2488G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117768 | |||||||
chr3:57117784 | G | A | 90 | a0002c0003t0032g0303 a0003c0002t0001g0016 a0003c0002t0001g0018 others(87): Show |
91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+2472C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117784 | |||||||
chr3:57117978 | A | G | 90 | a0002c0003t0032g0303 a0003c0002t0001g0016 a0003c0002t0001g0018 others(87): Show |
91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+2278T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117978 | |||||||
chr3:57118013 | C | T | 90 | a0002c0003t0032g0303 a0003c0002t0001g0016 a0003c0002t0001g0018 others(87): Show |
91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+2243G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118013 | |||||||
chr3:57118231 | A | C | 1 | a0002c0003t0002g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.184+2025T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118231 | |||||||
chr3:57118232 | C | A | 1 | a0002c0003t0002g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.184+2024G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118232 | |||||||
chr3:57118387 | G | T | 4 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0323 others(1): Show |
4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+1869C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118387 | |||||||
chr3:57118440 | C | A | 5 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+1816G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118440 | |||||||
chr3:57118503 | C | A | 264 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(261): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.184+1753G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118503 | |||||||
chr3:57118503 | C | T | 1 | a0002c0003t0002g0277 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.184+1753G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118503 | |||||||
chr3:57118965 | G | A | 1 | a0008c0017t0002g0252 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.184+1291C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118965 | |||||||
chr3:57119008 | C | T | 1 | a0001c0001t0007g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.184+1248G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119008 | |||||||
chr3:57119036 | T | G | 9 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.184+1220A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119036 | |||||||
chr3:57119070 | T | G | 1 | a0002c0003t0002g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.184+1186A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119070 | |||||||
chr3:57119078 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.184+1178G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119078 | |||||||
chr3:57119080 | C | T | 5 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0310 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+1176G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119080 | |||||||
chr3:57119351 | C | CA | 88 | a0001c0001t0004g0282 a0001c0001t0005g0159 a0001c0001t0046g0309 others(85): Show |
89 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.184+904dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119351 | |||||||
chr3:57119360 | C | A | 254 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(251): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.184+896G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119360 | |||||||
chr3:57119418 | G | A | 1 | a0003c0002t0001g0025 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.184+838C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119418 | |||||||
chr3:57119553 | G | A | 248 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(245): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.184+703C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119553 | |||||||
chr3:57119632 | C | A | 7 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.184+624G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119632 | |||||||
chr3:57119653 | G | GTTTCACA others(19): Show |
1 | a0002c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.184+577_184+602dup others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119653 | |||||||
chr3:57119653 | GTTTCACA others(19): Show |
G | 169 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.184+577_184+602del others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119653 | |||||||
chr3:57119654 | T | A | 90 | a0002c0003t0032g0303 a0003c0002t0001g0016 a0003c0002t0001g0018 others(87): Show |
91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+602A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119654 | |||||||
chr3:57119680 | T | A | 158 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(155): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.184+576A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119680 | |||||||
chr3:57119841 | C | T | 90 | a0002c0003t0032g0303 a0003c0002t0001g0016 a0003c0002t0001g0018 others(87): Show |
91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+415G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119841 | |||||||
chr3:57119992 | A | G | 5 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+264T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119992 | |||||||
chr3:57120156 | C | A | 2 | a0002c0003t0013g0063 a0002c0003t0013g0324 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.184+100G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57120156 | |||||||
chr3:57120330 | G | A | 1 | a0002c0003t0012g0156 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-17C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120330 | |||||||
chr3:57120637 | C | T | 1 | a0002c0003t0002g0073 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.127-324G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120637 | |||||||
chr3:57120730 | C | T | 7 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-417G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120730 | |||||||
chr3:57120794 | A | G | 285 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(282): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.127-481T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120794 | |||||||
chr3:57120850 | C | T | 89 | a0003c0002t0001g0016 a0003c0002t0001g0018 a0003c0002t0001g0024 others(86): Show |
90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.127-537G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120850 | |||||||
chr3:57121392 | G | C | 4 | a0001c0006t0011g0010 a0001c0006t0011g0011 a0001c0006t0011g0013 others(1): Show |
4 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1079C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57121392 | |||||||
chr3:57121816 | C | T | 3 | a0003c0002t0001g0295 a0003c0002t0001g0296 a0003c0002t0001g0297 |
3 | HG01496.hp2 HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.127-1503G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57121816 | |||||||
chr3:57122014 | G | T | 8 | a0001c0001t0004g0226 a0001c0001t0038g0035 a0001c0006t0011g0010 others(5): Show |
8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-1701C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122014 | |||||||
chr3:57122130 | G | C | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-1817C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122130 | |||||||
chr3:57122275 | G | C | 9 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-1962C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122275 | |||||||
chr3:57122338 | C | T | 3 | a0002c0003t0002g0337 a0002c0003t0002g0338 a0002c0003t0002g0339 |
3 | NA18974.hp1 NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.127-2025G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122338 | |||||||
chr3:57122473 | G | A | 1 | a0001c0001t0038g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-2160C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122473 | |||||||
chr3:57122491 | A | G | 7 | a0002c0004t0008g0077 a0002c0004t0008g0215 a0002c0004t0008g0264 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-2178T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122491 | |||||||
chr3:57122507 | T | C | 266 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(263): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.127-2194A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122507 | |||||||
chr3:57122740 | C | CT | 34 | a0002c0003t0002g0114 a0002c0003t0002g0308 a0002c0003t0013g0063 others(31): Show |
34 | HG01069.hp1 HG01081.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-2428dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122740 | |||||||
chr3:57122740 | C | CTT | 99 | a0001c0001t0003g0256 a0001c0001t0003g0286 a0001c0001t0004g0207 others(96): Show |
100 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.127-2429_127-2428d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122740 | |||||||
chr3:57122740 | C | CTTT | 145 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(142): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.127-2430_127-2428d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122740 | |||||||
chr3:57123128 | G | C | 42 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(39): Show |
42 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-2815C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123128 | |||||||
chr3:57123128 | G | T | 1 | a0003c0002t0001g0176 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.127-2815C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123128 | |||||||
chr3:57123307 | G | C | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-2994C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123307 | |||||||
chr3:57123333 | T | A | 1 | a0002c0007t0009g0312 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-3020A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123333 | |||||||
chr3:57123344 | C | G | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.127-3031G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123344 | |||||||
chr3:57123493 | C | T | 1 | a0002c0003t0002g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127-3180G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123493 | |||||||
chr3:57123496 | T | C | 1 | a0002c0003t0002g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127-3183A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123496 | |||||||
chr3:57123499 | C | T | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-3186G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123499 | |||||||
chr3:57123688 | G | A | 36 | a0001c0001t0004g0004 a0001c0001t0004g0045 a0001c0001t0004g0101 others(33): Show |
37 | HG00544.hp1 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.127-3375C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123688 | |||||||
chr3:57123950 | C | T | 91 | a0001c0001t0004g0190 a0001c0001t0045g0193 a0003c0002t0001g0016 others(88): Show |
92 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.127-3637G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123950 | |||||||
chr3:57123951 | G | A | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-3638C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123951 | |||||||
chr3:57123999 | C | T | 1 | a0002c0003t0012g0156 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-3686G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123999 | |||||||
chr3:57124156 | A | G | 1 | a0001c0001t0018g0331 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-3843T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124156 | |||||||
chr3:57124168 | C | T | 112 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(109): Show |
115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.127-3855G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124168 | |||||||
chr3:57124220 | A | G | 120 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(117): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.127-3907T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124220 | |||||||
chr3:57124309 | G | C | 224 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.127-3996C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124309 | |||||||
chr3:57124350 | T | C | 4 | a0002c0003t0002g0134 a0002c0003t0002g0301 a0002c0003t0002g0305 others(1): Show |
4 | HG00558.hp2 NA18980.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-4037A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124350 | |||||||
chr3:57124364 | C | T | 1 | a0002c0004t0008g0264 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.127-4051G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124364 | |||||||
chr3:57124525 | GA | G | 199 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(196): Show |
203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.127-4213delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124525 | |||||||
chr3:57124558 | G | A | 22 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0107 others(19): Show |
22 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-4245C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124558 | |||||||
chr3:57124657 | C | T | 105 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(102): Show |
108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.127-4344G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124657 | |||||||
chr3:57124903 | A | G | 3 | a0001c0001t0004g0190 a0003c0002t0001g0070 a0003c0002t0001g0189 |
3 | HG01081.hp1 HG01981.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.127-4590T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124903 | |||||||
chr3:57124991 | A | G | 1 | a0001c0001t0003g0334 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-4678T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124991 | |||||||
chr3:57125116 | A | G | 2 | a0001c0001t0006g0263 a0002c0004t0057g0287 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.127-4803T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125116 | |||||||
chr3:57125119 | T | C | 1 | a0002c0004t0051g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127-4806A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125119 | |||||||
chr3:57125224 | T | C | 1 | a0001c0001t0005g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.127-4911A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125224 | |||||||
chr3:57125236 | G | A | 87 | a0001c0001t0004g0190 a0001c0001t0020g0022 a0001c0001t0020g0212 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-4923C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125236 | |||||||
chr3:57125268 | G | T | 2 | a0002c0003t0014g0185 a0002c0003t0054g0021 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.127-4955C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125268 | |||||||
chr3:57125283 | T | C | 11 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-4970A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125283 | |||||||
chr3:57125412 | GA | G | 11 | a0002c0003t0002g0037 a0002c0003t0002g0072 a0002c0003t0013g0078 others(8): Show |
11 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-5100delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125412 | |||||||
chr3:57125434 | A | G | 1 | a0002c0003t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-5121T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125434 | |||||||
chr3:57125944 | T | C | 1 | a0005c0005t0010g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127-5631A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125944 | |||||||
chr3:57126089 | C | T | 27 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(24): Show |
29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-5776G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126089 | |||||||
chr3:57126123 | G | A | 7 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0107 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-5810C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126123 | |||||||
chr3:57126284 | T | C | 165 | a0001c0001t0003g0111 a0001c0001t0004g0004 a0001c0001t0004g0045 others(162): Show |
167 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(164): Show |
intron_variant | MODIFIER | c.127-5971A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126284 | |||||||
chr3:57126430 | C | A | 39 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(36): Show |
39 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.127-6117G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126430 | |||||||
chr3:57126443 | C | A | 44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-6130G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126443 | |||||||
chr3:57126454 | C | T | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6141G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126454 | |||||||
chr3:57126538 | C | A | 1 | a0002c0003t0022g0216 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-6225G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126538 | |||||||
chr3:57126774 | GTGAACAG others(60): Show |
G | 1 | a0003c0002t0015g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-6528_127-6462d others(69): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126774 | |||||||
chr3:57126950 | G | A | 1 | a0001c0001t0005g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.127-6637C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126950 | |||||||
chr3:57126975 | C | G | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-6662G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126975 | |||||||
chr3:57127056 | C | T | 1 | a0002c0003t0013g0078 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-6743G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127056 | |||||||
chr3:57127181 | C | CAT | 9 | a0001c0001t0005g0196 a0001c0001t0018g0331 a0002c0003t0002g0073 others(6): Show |
9 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-6870_127-6869d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127181 | |||||||
chr3:57127181 | C | CATAT | 27 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(24): Show |
29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-6872_127-6869d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127181 | |||||||
chr3:57127181 | CAT | C | 5 | a0001c0001t0046g0309 a0002c0004t0019g0006 a0002c0004t0019g0007 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6870_127-6869d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127181 | |||||||
chr3:57127189 | T | TATATATA others(15): Show |
1 | a0002c0003t0002g0251 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.127-6898_127-6877d others(24): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127189 | |||||||
chr3:57127189 | T | TATATATA others(25): Show |
1 | a0001c0001t0033g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-6908_127-6877d others(34): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127189 | |||||||
chr3:57127189 | TATATATA others(37): Show |
T | 5 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0326 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6920_127-6877d others(46): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127189 | |||||||
chr3:57127197 | T | A | 112 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(109): Show |
113 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.127-6884A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127197 | |||||||
chr3:57127201 | T | A | 13 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(10): Show |
13 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-6888A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127201 | |||||||
chr3:57127207 | TAA | T | 22 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0013g0325 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-6896_127-6895d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127207 | |||||||
chr3:57127209 | A | T | 9 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-6896T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127209 | |||||||
chr3:57127209 | AAAATATA others(3): Show |
A | 1 | a0001c0001t0004g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-6906_127-6897d others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127209 | |||||||
chr3:57127211 | A | T | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6898T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127211 | |||||||
chr3:57127219 | T | A | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6906A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127219 | |||||||
chr3:57127221 | A | T | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6908T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127221 | |||||||
chr3:57127233 | A | AAT | 7 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-6922_127-6921d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | |||||||
chr3:57127233 | A | AATATATA others(27): Show |
1 | a0002c0003t0002g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.127-6921_127-6920i others(36): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | |||||||
chr3:57127233 | A | T | 6 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(3): Show |
6 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-6920T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | |||||||
chr3:57127233 | AATATATA others(5): Show |
A | 1 | a0001c0001t0004g0231 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.127-6932_127-6921d others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | |||||||
chr3:57127239 | T | TA | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6927dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127239 | |||||||
chr3:57127239 | T | TATA | 35 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(32): Show |
35 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.127-6927_127-6926i others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127239 | |||||||
chr3:57127243 | T | A | 119 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0002 others(116): Show |
122 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.127-6930A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127243 | |||||||
chr3:57127245 | T | A | 83 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(80): Show |
84 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.127-6932A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127245 | |||||||
chr3:57127251 | T | A | 9 | a0001c0001t0037g0041 a0002c0003t0002g0202 a0002c0004t0008g0077 others(6): Show |
9 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-6938A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127251 | |||||||
chr3:57127251 | T | TAAAAATA others(17): Show |
26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-6939_127-6938i others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127251 | |||||||
chr3:57127253 | A | T | 1 | a0002c0003t0013g0325 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.127-6940T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127253 | |||||||
chr3:57127257 | T | A | 1 | a0002c0003t0013g0325 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.127-6944A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127257 | |||||||
chr3:57127261 | T | TA | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-6949dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127261 | |||||||
chr3:57127263 | AATATATA others(13): Show |
A | 1 | a0001c0001t0052g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-6970_127-6951d others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127263 | |||||||
chr3:57127263 | AATATATA others(39): Show |
A | 9 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-6996_127-6951d others(48): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127263 | |||||||
chr3:57127263 | AATATATA others(51): Show |
A | 29 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(26): Show |
29 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-7008_127-6951d others(60): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127263 | |||||||
chr3:57127271 | TA | T | 3 | a0002c0003t0002g0316 a0002c0004t0049g0168 a0003c0002t0001g0169 |
3 | HG00544.hp2 HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-6959delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127271 | |||||||
chr3:57127273 | A | T | 88 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(85): Show |
89 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-6960T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127273 | |||||||
chr3:57127273 | AAAATATA others(3): Show |
A | 18 | a0001c0001t0003g0293 a0001c0001t0004g0004 a0001c0001t0004g0190 others(15): Show |
19 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-6970_127-6961d others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127273 | |||||||
chr3:57127275 | A | T | 3 | a0002c0004t0049g0168 a0002c0004t0057g0287 a0003c0002t0001g0169 |
3 | HG01109.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-6962T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127275 | |||||||
chr3:57127283 | T | A | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-6970A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127283 | |||||||
chr3:57127283 | T | TAAATATA others(91): Show |
4 | a0002c0004t0008g0264 a0002c0004t0008g0298 a0002c0004t0008g0321 others(1): Show |
4 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-6971_127-6970i others(100): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127283 | |||||||
chr3:57127285 | A | T | 1 | a0001c0001t0004g0207 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.127-6972T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127285 | |||||||
chr3:57127286 | AT | A | 5 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0326 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6974delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127286 | |||||||
chr3:57127289 | T | TAA | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-6977_127-6976i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127289 | |||||||
chr3:57127293 | T | A | 1 | a0001c0001t0043g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.127-6980A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127293 | |||||||
chr3:57127295 | A | T | 92 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(89): Show |
93 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.127-6982T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127295 | |||||||
chr3:57127297 | T | A | 21 | a0001c0001t0004g0045 a0001c0001t0004g0101 a0001c0001t0004g0102 others(18): Show |
21 | HG00738.hp2 HG01255.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-6984A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127297 | |||||||
chr3:57127297 | TATATATA others(3): Show |
T | 4 | a0001c0001t0003g0258 a0001c0001t0003g0259 a0001c0001t0056g0246 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6994_127-6985d others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127297 | |||||||
chr3:57127297 | TATATATA others(55): Show |
T | 1 | a0002c0003t0013g0325 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.127-7046_127-6985d others(64): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127297 | |||||||
chr3:57127299 | T | A | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-6986A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127299 | |||||||
chr3:57127305 | A | T | 110 | a0001c0001t0004g0045 a0001c0001t0004g0101 a0001c0001t0004g0102 others(107): Show |
111 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(108): Show |
intron_variant | MODIFIER | c.127-6992T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127305 | |||||||
chr3:57127305 | AAAAT | A | 5 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0326 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6996_127-6993d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127305 | |||||||
chr3:57127307 | A | T | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0049g0168 others(1): Show |
4 | HG01109.hp1 HG03041.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6994T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127307 | |||||||
chr3:57127307 | AATATATA others(15): Show |
A | 1 | a0002c0003t0002g0238 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.127-7016_127-6995d others(24): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127307 | |||||||
chr3:57127313 | TA | T | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7001delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127313 | |||||||
chr3:57127315 | A | T | 42 | a0001c0001t0004g0004 a0001c0001t0004g0045 a0001c0001t0004g0101 others(39): Show |
43 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.127-7002T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127315 | |||||||
chr3:57127316 | A | T | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7003T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127316 | |||||||
chr3:57127317 | A | T | 14 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(11): Show |
14 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-7004T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127317 | |||||||
chr3:57127335 | T | A | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7022A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127335 | |||||||
chr3:57127335 | TAAA | T | 14 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(11): Show |
14 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-7025_127-7023d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127335 | |||||||
chr3:57127336 | A | ATATAT | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7024_127-7023i others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127336 | |||||||
chr3:57127337 | A | T | 31 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(28): Show |
31 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.127-7024T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127337 | |||||||
chr3:57127338 | A | T | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7025T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127338 | |||||||
chr3:57127339 | A | T | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7026T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127339 | |||||||
chr3:57127345 | T | A | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7032A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127345 | |||||||
chr3:57127347 | TA | T | 9 | a0001c0001t0003g0111 a0001c0001t0027g0167 a0001c0001t0038g0035 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7035delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127347 | |||||||
chr3:57127349 | A | AT | 20 | a0001c0001t0004g0315 a0001c0006t0011g0010 a0001c0006t0011g0011 others(17): Show |
20 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.127-7037_127-7036i others(3): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127349 | |||||||
chr3:57127355 | T | TAA | 83 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(80): Show |
84 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(81): Show |
intron_variant | MODIFIER | c.127-7043_127-7042i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127355 | |||||||
chr3:57127355 | TATAA | T | 13 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(10): Show |
13 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-7046_127-7043d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127355 | |||||||
chr3:57127357 | T | A | 23 | a0001c0001t0004g0315 a0001c0006t0011g0010 a0001c0006t0011g0011 others(20): Show |
23 | HG00673.hp2 HG01109.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-7044A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127357 | |||||||
chr3:57127359 | A | T | 25 | a0001c0001t0004g0315 a0001c0006t0011g0010 a0001c0006t0011g0011 others(22): Show |
25 | HG00673.hp2 HG01109.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-7046T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127359 | |||||||
chr3:57127359 | AATATAAA others(5): Show |
A | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7058_127-7047d others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127359 | |||||||
chr3:57127361 | T | A | 16 | a0002c0003t0002g0093 a0002c0003t0012g0034 a0002c0003t0012g0059 others(13): Show |
16 | HG00673.hp2 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-7048A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | |||||||
chr3:57127361 | T | TATATATA others(266): Show |
1 | a0002c0004t0008g0320 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.127-7049_127-7048i others(275): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | |||||||
chr3:57127361 | T | TATATATA others(266): Show |
1 | a0002c0004t0008g0077 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.127-7049_127-7048i others(275): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | |||||||
chr3:57127361 | T | TATATATA others(148): Show |
4 | a0002c0004t0008g0264 a0002c0004t0008g0298 a0002c0004t0008g0321 others(1): Show |
4 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-7049_127-7048i others(157): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | |||||||
chr3:57127363 | TAA | T | 9 | a0001c0001t0003g0111 a0001c0001t0027g0167 a0001c0001t0038g0035 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7052_127-7051d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127363 | |||||||
chr3:57127365 | A | AATAT | 9 | a0001c0001t0007g0003 a0001c0001t0007g0031 a0001c0001t0007g0032 others(6): Show |
10 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-7056_127-7053d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | |||||||
chr3:57127365 | A | T | 83 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(80): Show |
84 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.127-7052T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | |||||||
chr3:57127365 | AAT | A | 3 | a0001c0001t0004g0231 a0002c0003t0054g0021 a0003c0002t0001g0118 |
3 | HG03471.hp1 HG03490.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.127-7054_127-7053d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | |||||||
chr3:57127365 | AATAT | A | 5 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0334 others(2): Show |
5 | HG01934.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-7056_127-7053d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | |||||||
chr3:57127367 | T | TAA | 81 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(78): Show |
82 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.127-7055_127-7054i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127367 | |||||||
chr3:57127369 | T | A | 30 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(27): Show |
30 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-7056A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127369 | |||||||
chr3:57127369 | T | TATATAAA others(58): Show |
28 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(25): Show |
30 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-7057_127-7056i others(67): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127369 | |||||||
chr3:57127371 | T | A | 19 | a0002c0003t0002g0093 a0002c0003t0012g0034 a0002c0003t0012g0059 others(16): Show |
19 | HG00673.hp2 HG01255.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.127-7058A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127371 | |||||||
chr3:57127373 | T | A | 9 | a0001c0001t0003g0111 a0001c0001t0027g0167 a0001c0001t0038g0035 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7060A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127373 | |||||||
chr3:57127375 | T | A | 125 | a0001c0001t0004g0315 a0001c0001t0020g0022 a0001c0001t0020g0212 others(122): Show |
126 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.127-7062A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127375 | |||||||
chr3:57127375 | TATAA | T | 12 | a0001c0001t0003g0104 a0001c0001t0007g0003 a0001c0001t0007g0032 others(9): Show |
13 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-7066_127-7063d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127375 | |||||||
chr3:57127377 | T | C | 1 | a0001c0001t0004g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.127-7064A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127377 | |||||||
chr3:57127379 | A | T | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-7066T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127379 | |||||||
chr3:57127383 | A | T | 28 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(25): Show |
30 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-7070T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127383 | |||||||
chr3:57127387 | A | T | 5 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0326 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-7074T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127387 | |||||||
chr3:57127391 | A | T | 17 | a0001c0001t0004g0315 a0002c0003t0013g0078 a0002c0003t0013g0324 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.127-7078T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127391 | |||||||
chr3:57127395 | A | AAT | 31 | a0001c0001t0004g0004 a0001c0001t0004g0045 a0001c0001t0004g0101 others(28): Show |
32 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-7084_127-7083d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127395 | |||||||
chr3:57127395 | A | T | 46 | a0001c0001t0003g0111 a0001c0001t0004g0102 a0001c0001t0004g0315 others(43): Show |
46 | HG00609.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.127-7082T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127395 | |||||||
chr3:57127395 | AAT | A | 5 | a0002c0003t0014g0170 a0002c0003t0014g0185 a0002c0003t0053g0171 others(2): Show |
5 | HG01109.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-7084_127-7083d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127395 | |||||||
chr3:57127399 | T | A | 90 | a0001c0001t0003g0334 a0001c0001t0020g0022 a0001c0001t0020g0212 others(87): Show |
91 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.127-7086A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127399 | |||||||
chr3:57127406 | A | T | 1 | a0002c0007t0009g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-7093T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127406 | |||||||
chr3:57127408 | A | AT | 3 | a0002c0003t0013g0324 a0002c0003t0013g0326 a0002c0003t0021g0340 |
3 | HG02717.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.127-7096dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127408 | |||||||
chr3:57127408 | A | T | 2 | a0002c0004t0019g0006 a0002c0007t0009g0183 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.127-7095T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127408 | |||||||
chr3:57127410 | A | ATT | 4 | a0001c0001t0004g0210 a0001c0001t0004g0275 a0001c0001t0027g0167 others(1): Show |
4 | HG01123.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-7098_127-7097i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127410 | |||||||
chr3:57127410 | A | T | 20 | a0001c0001t0003g0307 a0001c0001t0004g0315 a0001c0001t0005g0214 others(17): Show |
20 | HG00544.hp2 HG01884.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-7097T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127410 | |||||||
chr3:57127411 | TA | T | 7 | a0001c0006t0011g0010 a0001c0006t0011g0011 a0001c0006t0011g0012 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-7099delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127411 | |||||||
chr3:57127412 | A | ATATTTT | 25 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0039 others(22): Show |
27 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-7100_127-7099i others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | |||||||
chr3:57127412 | A | ATT | 9 | a0001c0001t0004g0184 a0001c0001t0034g0100 a0002c0007t0009g0074 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7101_127-7100d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | |||||||
chr3:57127412 | A | ATTTTTT | 6 | a0001c0001t0003g0111 a0002c0003t0002g0048 a0004c0008t0006g0044 others(3): Show |
6 | HG01243.hp2 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-7105_127-7100d others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | |||||||
chr3:57127412 | A | T | 142 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(139): Show |
145 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-7099T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | |||||||
chr3:57127412 | AT | A | 91 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(88): Show |
92 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.127-7100delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | |||||||
chr3:57127414 | T | A | 3 | a0001c0001t0004g0223 a0001c0001t0004g0224 a0001c0001t0037g0041 |
3 | HG01361.hp2 HG01516.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.127-7101A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127414 | |||||||
chr3:57127415 | T | A | 1 | a0003c0002t0001g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-7102A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127415 | |||||||
chr3:57127445 | G | A | 1 | a0003c0002t0001g0137 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.127-7132C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127445 | |||||||
chr3:57127551 | G | A | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-7238C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127551 | |||||||
chr3:57127597 | G | A | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-7284C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127597 | |||||||
chr3:57127859 | C | A | 1 | a0001c0001t0034g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127-7546G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127859 | |||||||
chr3:57127902 | T | C | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7589A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127902 | |||||||
chr3:57128144 | T | C | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-7831A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128144 | |||||||
chr3:57128146 | T | C | 1 | a0002c0003t0054g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127-7833A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128146 | |||||||
chr3:57128147 | G | A | 1 | a0002c0003t0012g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-7834C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128147 | |||||||
chr3:57128250 | G | A | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-7937C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128250 | |||||||
chr3:57128338 | A | G | 2 | a0001c0001t0003g0270 a0001c0001t0003g0336 |
2 | NA18949.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.127-8025T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128338 | |||||||
chr3:57128431 | G | A | 1 | a0002c0003t0002g0305 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.127-8118C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128431 | |||||||
chr3:57128443 | G | A | 27 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(24): Show |
29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-8130C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128443 | |||||||
chr3:57128448 | C | T | 86 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(83): Show |
87 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.127-8135G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128448 | |||||||
chr3:57128449 | G | A | 27 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(24): Show |
29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-8136C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128449 | |||||||
chr3:57128530 | C | T | 2 | a0003c0002t0001g0081 a0003c0002t0001g0131 |
2 | NA18970.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.127-8217G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128530 | |||||||
chr3:57128551 | C | CGAAATCC others(26): Show |
17 | a0002c0003t0002g0037 a0002c0003t0002g0038 a0002c0003t0002g0039 others(14): Show |
17 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.127-8271_127-8239d others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128551 | |||||||
chr3:57128576 | A | G | 2 | a0003c0002t0001g0125 a0003c0002t0001g0273 |
2 | HG02040.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.127-8263T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128576 | |||||||
chr3:57128706 | C | G | 4 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-8393G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128706 | |||||||
chr3:57128715 | A | G | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-8402T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128715 | |||||||
chr3:57128812 | C | A | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-8499G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128812 | |||||||
chr3:57128857 | C | T | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-8544G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128857 | |||||||
chr3:57129144 | A | T | 8 | a0001c0001t0052g0299 a0002c0003t0012g0221 a0005c0005t0010g0061 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-8831T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129144 | |||||||
chr3:57129173 | G | A | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-8860C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129173 | |||||||
chr3:57129303 | C | T | 1 | a0002c0003t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-8990G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129303 | |||||||
chr3:57129367 | A | G | 3 | a0003c0002t0001g0144 a0003c0002t0001g0146 a0003c0002t0015g0145 |
3 | HG02896.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.127-9054T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129367 | |||||||
chr3:57129566 | C | T | 2 | a0002c0003t0013g0324 a0002c0003t0014g0323 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.127-9253G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129566 | |||||||
chr3:57129669 | G | C | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-9356C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129669 | |||||||
chr3:57129671 | A | G | 6 | a0002c0003t0002g0086 a0003c0002t0001g0036 a0003c0002t0001g0051 others(3): Show |
6 | NA18962.hp2 NA18974.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-9358T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129671 | |||||||
chr3:57129723 | T | C | 167 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(164): Show |
170 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.127-9410A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129723 | |||||||
chr3:57129737 | C | T | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-9424G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129737 | |||||||
chr3:57129859 | G | T | 133 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(130): Show |
134 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(131): Show |
intron_variant | MODIFIER | c.127-9546C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129859 | |||||||
chr3:57129986 | C | T | 1 | a0003c0002t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-9673G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129986 | |||||||
chr3:57129996 | C | T | 1 | a0003c0002t0001g0211 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.127-9683G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129996 | |||||||
chr3:57130154 | C | A | 1 | a0001c0001t0004g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127-9841G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130154 | |||||||
chr3:57130229 | G | T | 2 | a0001c0001t0007g0150 a0001c0001t0007g0188 |
2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.127-9916C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130229 | |||||||
chr3:57130334 | C | T | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-10021G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130334 | |||||||
chr3:57130380 | A | T | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-10067T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130380 | |||||||
chr3:57130562 | G | A | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-10249C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130562 | |||||||
chr3:57130578 | G | C | 1 | a0002c0003t0002g0098 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127-10265C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130578 | |||||||
chr3:57130597 | G | A | 46 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(43): Show |
46 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.127-10284C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130597 | |||||||
chr3:57130667 | C | G | 5 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0310 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-10354G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130667 | |||||||
chr3:57130670 | G | A | 1 | a0001c0001t0003g0186 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.127-10357C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130670 | |||||||
chr3:57130771 | T | C | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-10458A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130771 | |||||||
chr3:57130821 | T | A | 27 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(24): Show |
29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-10508A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130821 | |||||||
chr3:57130901 | G | A | 133 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(130): Show |
134 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(131): Show |
intron_variant | MODIFIER | c.127-10588C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130901 | |||||||
chr3:57130931 | C | T | 4 | a0001c0001t0004g0184 a0001c0001t0004g0317 a0001c0001t0004g0318 others(1): Show |
4 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-10618G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130931 | |||||||
chr3:57131055 | G | A | 1 | a0003c0002t0001g0026 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127-10742C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131055 | |||||||
chr3:57131055 | G | C | 1 | a0001c0001t0005g0329 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-10742C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131055 | |||||||
chr3:57131063 | G | C | 1 | a0002c0003t0002g0098 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127-10750C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131063 | |||||||
chr3:57131216 | T | C | 44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-10903A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131216 | |||||||
chr3:57131232 | T | C | 6 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0325 others(3): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-10919A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131232 | |||||||
chr3:57131278 | G | A | 1 | a0001c0001t0039g0268 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.127-10965C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131278 | |||||||
chr3:57131279 | C | T | 1 | a0001c0001t0025g0347 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-10966G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131279 | |||||||
chr3:57131282 | C | A | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-10969G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131282 | |||||||
chr3:57131329 | C | G | 1 | a0003c0002t0001g0143 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.127-11016G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131329 | |||||||
chr3:57131540 | T | G | 1 | a0002c0003t0002g0302 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.127-11227A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131540 | |||||||
chr3:57131627 | C | T | 3 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0053g0171 |
3 | HG01109.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.127-11314G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131627 | |||||||
chr3:57131654 | G | A | 1 | a0001c0001t0003g0289 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127-11341C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131654 | |||||||
chr3:57131787 | C | T | 2 | a0003c0002t0001g0146 a0003c0002t0015g0145 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.127-11474G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131787 | |||||||
chr3:57131837 | T | C | 1 | a0002c0003t0002g0338 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.127-11524A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131837 | |||||||
chr3:57131882 | C | T | 1 | a0006c0014t0018g0330 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-11569G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131882 | |||||||
chr3:57132113 | G | A | 1 | a0002c0003t0012g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-11800C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132113 | |||||||
chr3:57132125 | G | A | 3 | a0001c0001t0004g0223 a0001c0001t0004g0224 a0001c0001t0004g0275 |
3 | HG01361.hp2 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.127-11812C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132125 | |||||||
chr3:57132195 | G | A | 1 | a0002c0003t0014g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.127-11882C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132195 | |||||||
chr3:57132198 | C | T | 1 | a0001c0001t0052g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-11885G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132198 | |||||||
chr3:57132300 | C | CA | 9 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-11988dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132300 | |||||||
chr3:57132320 | C | T | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-12007G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132320 | |||||||
chr3:57132352 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-12039G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132352 | |||||||
chr3:57132353 | G | A | 2 | a0001c0001t0005g0199 a0001c0001t0005g0200 |
2 | NA18943.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.127-12040C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132353 | |||||||
chr3:57132415 | G | A | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-12102C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132415 | |||||||
chr3:57132587 | T | C | 4 | a0002c0004t0019g0006 a0002c0004t0019g0007 a0002c0004t0048g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-12274A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132587 | |||||||
chr3:57132604 | T | C | 1 | a0001c0001t0003g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.127-12291A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132604 | |||||||
chr3:57132929 | G | A | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-12616C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132929 | |||||||
chr3:57133111 | A | T | 1 | a0002c0003t0012g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-12798T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133111 | |||||||
chr3:57133112 | C | G | 1 | a0002c0003t0012g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-12799G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133112 | |||||||
chr3:57133113 | A | T | 1 | a0002c0003t0012g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-12800T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133113 | |||||||
chr3:57133364 | T | C | 44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-13051A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133364 | |||||||
chr3:57133401 | G | GCA | 3 | a0002c0003t0022g0097 a0002c0003t0022g0216 a0002c0003t0055g0009 |
3 | HG02622.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.127-13090_127-1308 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133401 | |||||||
chr3:57133403 | A | G | 1 | a0002c0003t0002g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.127-13090T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133403 | |||||||
chr3:57133456 | T | C | 1 | a0003c0002t0001g0116 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.127-13143A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133456 | |||||||
chr3:57133674 | C | G | 3 | a0002c0004t0008g0264 a0002c0004t0008g0298 a0002c0004t0008g0322 |
3 | HG00099.hp1 HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.127-13361G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133674 | |||||||
chr3:57133703 | T | A | 2 | a0002c0004t0008g0320 a0002c0004t0008g0321 |
2 | HG03017.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.127-13390A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133703 | |||||||
chr3:57133709 | G | C | 5 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(2): Show |
5 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-13396C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133709 | |||||||
chr3:57133723 | A | C | 1 | a0006c0014t0018g0330 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-13410T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133723 | |||||||
chr3:57133915 | G | T | 3 | a0003c0002t0001g0219 a0003c0002t0015g0220 a0003c0002t0015g0290 |
3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.127-13602C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133915 | |||||||
chr3:57133951 | T | C | 1 | a0001c0001t0003g0234 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.127-13638A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133951 | |||||||
chr3:57134126 | G | A | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-13813C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134126 | |||||||
chr3:57134245 | T | C | 167 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(164): Show |
170 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.127-13932A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134245 | |||||||
chr3:57134311 | C | A | 1 | a0001c0001t0043g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.127-13998G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134311 | |||||||
chr3:57134313 | C | T | 134 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(131): Show |
135 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.127-14000G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134313 | |||||||
chr3:57134518 | A | G | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14205T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134518 | |||||||
chr3:57134564 | C | T | 4 | a0002c0003t0002g0093 a0003c0002t0001g0219 a0003c0002t0015g0220 others(1): Show |
4 | HG01169.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14251G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134564 | |||||||
chr3:57134643 | C | T | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14330G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134643 | |||||||
chr3:57134706 | G | T | 1 | a0001c0001t0005g0196 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.127-14393C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134706 | |||||||
chr3:57134765 | G | A | 130 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(127): Show |
131 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.127-14452C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134765 | |||||||
chr3:57135118 | AAAAC | A | 4 | a0002c0003t0002g0093 a0003c0002t0001g0219 a0003c0002t0015g0220 others(1): Show |
4 | HG01169.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14809_127-1480 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135118 | |||||||
chr3:57135145 | C | CA | 114 | a0001c0001t0004g0315 a0001c0001t0020g0022 a0001c0001t0020g0212 others(111): Show |
115 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.127-14833dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135145 | |||||||
chr3:57135145 | C | CAA | 10 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-14834_127-1483 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135145 | |||||||
chr3:57135146 | A | AC | 5 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(2): Show |
5 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-14834_127-1483 others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135146 | |||||||
chr3:57135185 | C | T | 1 | a0003c0002t0001g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.127-14872G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135185 | |||||||
chr3:57135206 | C | G | 1 | a0003c0002t0001g0218 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127-14893G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135206 | |||||||
chr3:57135245 | C | A | 1 | a0001c0001t0004g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.127-14932G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135245 | |||||||
chr3:57135412 | G | C | 8 | a0002c0003t0002g0195 a0002c0003t0002g0262 a0002c0003t0002g0283 others(5): Show |
8 | HG02165.hp1 NA18974.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-15099C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135412 | |||||||
chr3:57135488 | G | A | 1 | a0001c0001t0033g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-15175C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135488 | |||||||
chr3:57135575 | C | T | 1 | a0003c0002t0001g0079 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.127-15262G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135575 | |||||||
chr3:57135620 | T | C | 93 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0001c0001t0027g0167 others(90): Show |
94 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.127-15307A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135620 | |||||||
chr3:57135742 | C | T | 3 | a0002c0003t0002g0276 a0002c0003t0002g0277 a0002c0015t0002g0278 |
3 | HG02165.hp2 NA18959.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.127-15429G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135742 | |||||||
chr3:57135857 | C | T | 1 | a0001c0001t0004g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-15544G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135857 | |||||||
chr3:57135858 | G | A | 1 | a0001c0001t0027g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-15545C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135858 | |||||||
chr3:57135889 | G | GTGTA | 134 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(131): Show |
135 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.127-15577_127-1557 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135889 | |||||||
chr3:57135963 | C | T | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-15650G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135963 | |||||||
chr3:57136261 | C | T | 7 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0325 others(4): Show |
7 | HG01109.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-15948G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136261 | |||||||
chr3:57136373 | C | T | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-16060G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136373 | |||||||
chr3:57136416 | C | A | 6 | a0003c0002t0001g0128 a0003c0002t0001g0135 a0003c0002t0001g0136 others(3): Show |
6 | HG01074.hp1 HG01192.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-16103G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136416 | |||||||
chr3:57136467 | G | C | 132 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(129): Show |
133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-16154C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136467 | |||||||
chr3:57136641 | C | CA | 28 | a0001c0001t0003g0270 a0001c0001t0003g0289 a0001c0001t0003g0336 others(25): Show |
29 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-16329dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | |||||||
chr3:57136641 | CA | C | 43 | a0001c0001t0003g0234 a0001c0001t0003g0256 a0001c0001t0004g0102 others(40): Show |
44 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.127-16329delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | |||||||
chr3:57136641 | CAA | C | 75 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0001c0001t0027g0167 others(72): Show |
75 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.127-16330_127-1632 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | |||||||
chr3:57136641 | CAAA | C | 15 | a0002c0003t0002g0093 a0002c0003t0012g0034 a0002c0003t0012g0059 others(12): Show |
15 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-16331_127-1632 others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | |||||||
chr3:57136641 | CAAAA | C | 34 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0002g0204 others(31): Show |
34 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-16332_127-1632 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | |||||||
chr3:57136641 | CAAAAA | C | 23 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(20): Show |
25 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-16333_127-1632 others(9): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | |||||||
chr3:57136712 | C | T | 4 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-16399G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136712 | |||||||
chr3:57136716 | T | C | 2 | a0001c0001t0003g0253 a0001c0001t0026g0267 |
2 | HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.127-16403A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136716 | |||||||
chr3:57136738 | T | G | 18 | a0002c0003t0002g0037 a0002c0003t0002g0038 a0002c0003t0002g0039 others(15): Show |
18 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-16425A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136738 | |||||||
chr3:57136863 | A | G | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-16550T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136863 | |||||||
chr3:57136879 | G | C | 128 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(125): Show |
129 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.127-16566C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136879 | |||||||
chr3:57136881 | TAA | T | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-16570_127-1656 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136881 | |||||||
chr3:57136924 | A | T | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-16611T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136924 | |||||||
chr3:57137048 | C | T | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-16735G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137048 | |||||||
chr3:57137062 | G | T | 1 | a0002c0003t0002g0195 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.127-16749C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137062 | |||||||
chr3:57137297 | T | C | 5 | a0001c0001t0004g0226 a0001c0001t0006g0230 a0001c0001t0006g0263 others(2): Show |
5 | HG03098.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-16984A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137297 | |||||||
chr3:57137334 | G | A | 1 | a0003c0002t0001g0055 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.127-17021C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137334 | |||||||
chr3:57137343 | C | A | 1 | a0002c0007t0009g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127-17030G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137343 | |||||||
chr3:57137346 | G | A | 1 | a0002c0007t0009g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127-17033C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137346 | |||||||
chr3:57137378 | C | A | 32 | a0001c0001t0004g0004 a0001c0001t0004g0045 a0001c0001t0004g0101 others(29): Show |
33 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.127-17065G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137378 | |||||||
chr3:57137526 | G | C | 93 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0001c0001t0027g0167 others(90): Show |
94 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.127-17213C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137526 | |||||||
chr3:57137646 | C | A | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-17333G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137646 | |||||||
chr3:57137674 | A | G | 1 | a0001c0001t0052g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-17361T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137674 | |||||||
chr3:57137777 | G | A | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-17464C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137777 | |||||||
chr3:57137805 | C | T | 4 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-17492G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137805 | |||||||
chr3:57137874 | T | C | 132 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(129): Show |
133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-17561A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137874 | |||||||
chr3:57137967 | A | C | 4 | a0002c0003t0002g0093 a0003c0002t0001g0219 a0003c0002t0015g0220 others(1): Show |
4 | HG01169.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-17654T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137967 | |||||||
chr3:57138233 | TA | T | 3 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 |
3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.127-17921delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138233 | |||||||
chr3:57138419 | C | T | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-18106G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138419 | |||||||
chr3:57138511 | G | A | 1 | a0001c0001t0004g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.127-18198C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138511 | |||||||
chr3:57138517 | T | C | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-18204A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138517 | |||||||
chr3:57138543 | G | T | 4 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-18230C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138543 | |||||||
chr3:57138582 | A | G | 1 | a0002c0003t0014g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.127-18269T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138582 | |||||||
chr3:57138614 | C | T | 8 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0236 others(5): Show |
10 | HG00609.hp2 NA18941.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-18301G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138614 | |||||||
chr3:57138865 | G | A | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-18552C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138865 | |||||||
chr3:57138939 | C | CA | 24 | a0001c0001t0003g0107 a0001c0001t0004g0207 a0001c0001t0004g0317 others(21): Show |
24 | HG00642.hp1 HG01109.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.127-18627dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138939 | |||||||
chr3:57138939 | CA | C | 11 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0236 others(8): Show |
13 | HG00609.hp2 HG01074.hp2 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-18627delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138939 | |||||||
chr3:57138993 | A | T | 129 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(126): Show |
130 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.127-18680T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138993 | |||||||
chr3:57139064 | G | A | 11 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-18751C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139064 | |||||||
chr3:57139196 | C | G | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-18883G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139196 | |||||||
chr3:57139236 | C | T | 1 | a0002c0003t0002g0072 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.127-18923G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139236 | |||||||
chr3:57139322 | G | A | 1 | a0001c0001t0027g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-19009C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139322 | |||||||
chr3:57139515 | CT | C | 119 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0006g0106 others(116): Show |
120 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.127-19203delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139515 | |||||||
chr3:57139515 | CTT | C | 11 | a0002c0003t0002g0093 a0002c0003t0014g0170 a0002c0003t0014g0172 others(8): Show |
11 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-19204_127-1920 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139515 | |||||||
chr3:57139887 | T | C | 271 | a0001c0001t0003g0111 a0001c0001t0003g0256 a0001c0001t0003g0258 others(268): Show |
276 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(273): Show |
intron_variant | MODIFIER | c.127-19574A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139887 | |||||||
chr3:57139933 | G | C | 1 | a0002c0003t0002g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.127-19620C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139933 | |||||||
chr3:57140246 | T | C | 40 | a0001c0001t0005g0017 a0001c0001t0005g0033 a0001c0001t0005g0159 others(37): Show |
41 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-19933A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140246 | |||||||
chr3:57140259 | A | G | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-19946T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140259 | |||||||
chr3:57140449 | A | T | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-20136T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140449 | |||||||
chr3:57140608 | C | T | 1 | a0002c0003t0002g0283 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127-20295G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140608 | |||||||
chr3:57140785 | G | T | 1 | a0003c0002t0001g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-20472C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140785 | |||||||
chr3:57140823 | T | C | 1 | a0003c0002t0001g0140 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.127-20510A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140823 | |||||||
chr3:57140893 | C | CT | 133 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0001c0001t0027g0167 others(130): Show |
136 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.127-20581dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140893 | |||||||
chr3:57140893 | C | CTT | 11 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-20582_127-2058 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140893 | |||||||
chr3:57141087 | A | G | 1 | a0002c0003t0054g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127-20774T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141087 | |||||||
chr3:57141104 | G | A | 3 | a0002c0003t0013g0325 a0002c0003t0013g0326 a0002c0003t0021g0340 |
3 | HG02970.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-20791C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141104 | |||||||
chr3:57141170 | G | A | 6 | a0001c0001t0004g0223 a0001c0001t0004g0224 a0001c0001t0004g0231 others(3): Show |
6 | HG01361.hp2 HG01516.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-20857C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141170 | |||||||
chr3:57141426 | A | G | 88 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(85): Show |
89 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-21113T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141426 | |||||||
chr3:57141512 | A | G | 3 | a0002c0003t0002g0276 a0002c0003t0002g0277 a0002c0015t0002g0278 |
3 | HG02165.hp2 NA18959.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.127-21199T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141512 | |||||||
chr3:57141750 | T | C | 6 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0325 others(3): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-21437A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141750 | |||||||
chr3:57141846 | GA | G | 5 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(2): Show |
5 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-21534delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141846 | |||||||
chr3:57141860 | T | C | 11 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-21547A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141860 | |||||||
chr3:57141945 | A | G | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-21632T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141945 | |||||||
chr3:57141951 | G | A | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-21638C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141951 | |||||||
chr3:57142049 | C | T | 32 | a0001c0001t0004g0004 a0001c0001t0004g0045 a0001c0001t0004g0101 others(29): Show |
33 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.127-21736G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142049 | |||||||
chr3:57142056 | C | G | 9 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-21743G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142056 | |||||||
chr3:57142169 | G | A | 132 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(129): Show |
133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-21856C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142169 | |||||||
chr3:57142184 | C | T | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-21871G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142184 | |||||||
chr3:57142212 | C | T | 1 | a0003c0002t0001g0176 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.127-21899G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142212 | |||||||
chr3:57142309 | T | G | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-21996A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142309 | |||||||
chr3:57142361 | T | C | 1 | a0002c0003t0054g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127-22048A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142361 | |||||||
chr3:57142474 | C | T | 3 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0229 |
3 | HG00099.hp2 HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.127-22161G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142474 | |||||||
chr3:57142475 | G | A | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-22162C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142475 | |||||||
chr3:57142477 | A | G | 132 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(129): Show |
133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-22164T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142477 | |||||||
chr3:57142498 | G | A | 1 | a0003c0002t0001g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.127-22185C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142498 | |||||||
chr3:57142520 | A | G | 11 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-22207T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142520 | |||||||
chr3:57142528 | G | A | 9 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-22215C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142528 | |||||||
chr3:57142547 | G | A | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-22234C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142547 | |||||||
chr3:57142570 | C | T | 1 | a0002c0003t0032g0303 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.127-22257G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142570 | |||||||
chr3:57142597 | C | A | 1 | a0001c0001t0004g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127-22284G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142597 | |||||||
chr3:57142603 | G | C | 1 | a0002c0004t0051g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127-22290C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142603 | |||||||
chr3:57142719 | T | G | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-22406A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142719 | |||||||
chr3:57143068 | A | C | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.126+22093T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143068 | |||||||
chr3:57143143 | A | G | 88 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(85): Show |
89 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.126+22018T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143143 | |||||||
chr3:57143167 | C | T | 165 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(162): Show |
168 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.126+21994G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143167 | |||||||
chr3:57143316 | T | C | 1 | a0002c0003t0013g0063 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.126+21845A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143316 | |||||||
chr3:57143342 | TGACAATC others(14): Show |
T | 1 | a0009c0016t0002g0239 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.126+21798_126+2181 others(25): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143342 | |||||||
chr3:57143380 | G | T | 7 | a0001c0001t0004g0315 a0002c0003t0013g0078 a0002c0003t0013g0324 others(4): Show |
7 | HG02622.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+21781C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143380 | |||||||
chr3:57143423 | C | T | 6 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0325 others(3): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+21738G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143423 | |||||||
chr3:57143504 | C | T | 1 | a0002c0003t0053g0171 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+21657G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143504 | |||||||
chr3:57143522 | C | A | 3 | a0003c0002t0001g0117 a0003c0002t0001g0118 a0003c0002t0001g0119 |
3 | HG02735.hp2 NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+21639G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143522 | |||||||
chr3:57143615 | C | T | 2 | a0001c0001t0003g0256 a0007c0019t0003g0343 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.126+21546G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143615 | |||||||
chr3:57143688 | T | C | 84 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(81): Show |
85 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.126+21473A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143688 | |||||||
chr3:57143755 | G | A | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+21406C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143755 | |||||||
chr3:57143785 | G | A | 1 | a0004c0009t0003g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.126+21376C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143785 | |||||||
chr3:57143811 | G | C | 1 | a0003c0002t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+21350C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143811 | |||||||
chr3:57143954 | T | C | 1 | a0003c0002t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.126+21207A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143954 | |||||||
chr3:57144133 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126+21028G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144133 | |||||||
chr3:57144257 | CCT | C | 44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+20902_126+2090 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144257 | |||||||
chr3:57144265 | C | T | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.126+20896G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144265 | |||||||
chr3:57144328 | T | C | 1 | a0002c0003t0013g0078 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126+20833A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144328 | |||||||
chr3:57144368 | T | C | 11 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+20793A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144368 | |||||||
chr3:57144436 | G | T | 2 | a0003c0002t0001g0029 a0003c0002t0001g0089 |
2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.126+20725C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144436 | |||||||
chr3:57144670 | A | C | 19 | a0001c0001t0003g0256 a0001c0001t0003g0258 a0001c0001t0003g0259 others(16): Show |
19 | HG01099.hp1 HG01884.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+20491T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144670 | |||||||
chr3:57144692 | C | T | 1 | a0002c0003t0012g0221 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126+20469G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144692 | |||||||
chr3:57144727 | A | AGT | 344 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0104 others(341): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.126+20432_126+2043 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144727 | |||||||
chr3:57144773 | G | C | 3 | a0003c0002t0001g0117 a0003c0002t0001g0118 a0003c0002t0001g0119 |
3 | HG02735.hp2 NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+20388C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144773 | |||||||
chr3:57144976 | C | G | 1 | a0002c0003t0013g0324 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+20185G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144976 | |||||||
chr3:57145045 | C | G | 3 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 |
3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+20116G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145045 | |||||||
chr3:57145140 | G | A | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+20021C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145140 | |||||||
chr3:57145218 | T | A | 1 | a0003c0002t0001g0029 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.126+19943A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145218 | |||||||
chr3:57145233 | C | G | 132 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(129): Show |
133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.126+19928G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145233 | |||||||
chr3:57145402 | G | A | 8 | a0001c0001t0038g0035 a0001c0006t0011g0010 a0001c0006t0011g0011 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+19759C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145402 | |||||||
chr3:57145421 | G | A | 1 | a0001c0001t0035g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.126+19740C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145421 | |||||||
chr3:57145823 | G | A | 4 | a0002c0003t0014g0170 a0002c0003t0014g0172 a0002c0003t0014g0185 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+19338C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145823 | |||||||
chr3:57145922 | G | A | 1 | a0002c0004t0016g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.126+19239C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145922 | |||||||
chr3:57145923 | G | A | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+19238C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145923 | |||||||
chr3:57145933 | T | A | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+19228A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145933 | |||||||
chr3:57146019 | ACACACAC others(19): Show |
A | 1 | a0001c0001t0036g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126+19116_126+1914 others(30): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146019 | |||||||
chr3:57146027 | ACT | A | 4 | a0002c0004t0008g0077 a0002c0004t0008g0298 a0002c0004t0008g0321 others(1): Show |
4 | HG00099.hp1 HG00639.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+19132_126+1913 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146027 | |||||||
chr3:57146029 | T | G | 2 | a0002c0004t0008g0264 a0002c0004t0008g0320 |
2 | HG01099.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.126+19132A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146029 | |||||||
chr3:57146029 | T | TCACGCG | 9 | a0001c0006t0011g0010 a0001c0006t0011g0013 a0002c0003t0012g0156 others(6): Show |
9 | HG01109.hp2 HG01255.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+19126_126+1913 others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146029 | |||||||
chr3:57146031 | A | ACG | 34 | a0001c0001t0003g0015 a0001c0001t0003g0104 a0001c0001t0003g0253 others(31): Show |
34 | HG00544.hp2 HG00642.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.126+19128_126+1912 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146031 | |||||||
chr3:57146031 | A | ACGCGCAC others(3): Show |
1 | a0003c0002t0015g0290 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.126+19129_126+1913 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146031 | |||||||
chr3:57146031 | A | G | 6 | a0002c0004t0008g0077 a0002c0004t0008g0264 a0002c0004t0008g0298 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+19130T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146031 | |||||||
chr3:57146033 | G | GCGCA | 23 | a0001c0001t0003g0111 a0001c0001t0027g0167 a0001c0001t0038g0035 others(20): Show |
23 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+19127_126+1912 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146033 | |||||||
chr3:57146035 | G | GCACGCA | 11 | a0001c0001t0004g0315 a0002c0003t0013g0078 a0002c0003t0013g0324 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+19125_126+1912 others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146035 | |||||||
chr3:57146037 | G | A | 82 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(79): Show |
83 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.126+19124C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146037 | |||||||
chr3:57146041 | G | A | 2 | a0001c0001t0003g0186 a0001c0001t0046g0309 |
2 | HG02258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.126+19120C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146041 | |||||||
chr3:57146042 | C | T | 4 | a0002c0004t0019g0006 a0002c0004t0019g0007 a0002c0004t0048g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+19119G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146042 | |||||||
chr3:57146045 | G | A | 48 | a0001c0001t0005g0017 a0001c0001t0005g0033 a0001c0001t0005g0159 others(45): Show |
49 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.126+19116C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCACA | 5 | a0003c0002t0001g0016 a0003c0002t0001g0065 a0003c0002t0001g0083 others(2): Show |
5 | HG02083.hp1 NA18956.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+19112_126+1911 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCAC others(3): Show |
1 | a0002c0003t0054g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCAC others(5): Show |
1 | a0003c0002t0001g0173 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCGC others(3): Show |
27 | a0001c0001t0020g0212 a0003c0002t0001g0027 a0003c0002t0001g0049 others(24): Show |
27 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+19115_126+1911 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCGC others(5): Show |
3 | a0003c0002t0001g0018 a0003c0002t0001g0140 a0003c0002t0001g0273 |
3 | NA18971.hp1 NA19012.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.126+19115_126+1911 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCGC others(7): Show |
1 | a0003c0002t0001g0274 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCGC others(5): Show |
41 | a0001c0001t0020g0022 a0002c0003t0002g0086 a0002c0003t0002g0088 others(38): Show |
42 | HG00544.hp1 HG00673.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.126+19115_126+1911 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCGC others(7): Show |
4 | a0003c0002t0001g0028 a0003c0002t0001g0054 a0003c0002t0001g0058 others(1): Show |
4 | HG02074.hp2 NA18980.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+19115_126+1911 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCGCGCGC others(7): Show |
1 | a0003c0002t0001g0026 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146045 | G | GCTGCGCG others(6): Show |
1 | a0003c0002t0001g0218 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.126+19115_126+1911 others(17): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | |||||||
chr3:57146047 | A | G | 1 | a0001c0001t0003g0265 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.126+19114T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146047 | |||||||
chr3:57146132 | G | C | 44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+19029C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146132 | |||||||
chr3:57146144 | T | A | 33 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(30): Show |
35 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+19017A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146144 | |||||||
chr3:57146302 | G | A | 4 | a0002c0004t0016g0333 a0002c0004t0016g0341 a0002c0004t0016g0342 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+18859C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146302 | |||||||
chr3:57146374 | C | A | 122 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(119): Show |
123 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.126+18787G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146374 | |||||||
chr3:57146406 | T | A | 1 | a0001c0001t0005g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.126+18755A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146406 | |||||||
chr3:57146505 | C | G | 6 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0325 others(3): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+18656G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146505 | |||||||
chr3:57146519 | G | A | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+18642C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146519 | |||||||
chr3:57146639 | A | G | 1 | a0002c0004t0051g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+18522T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146639 | |||||||
chr3:57146657 | G | A | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.126+18504C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146657 | |||||||
chr3:57146749 | C | CA | 9 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0107 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+18411dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146749 | |||||||
chr3:57146749 | CA | C | 132 | a0001c0001t0004g0223 a0001c0001t0004g0315 a0001c0001t0020g0022 others(129): Show |
134 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.126+18411delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146749 | |||||||
chr3:57146749 | CAA | C | 17 | a0002c0003t0002g0088 a0002c0003t0002g0093 a0002c0003t0012g0034 others(14): Show |
18 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+18410_126+1841 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146749 | |||||||
chr3:57146762 | A | G | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+18399T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146762 | |||||||
chr3:57146797 | T | C | 1 | a0002c0003t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+18364A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146797 | |||||||
chr3:57146812 | G | C | 1 | a0003c0002t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.126+18349C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146812 | |||||||
chr3:57146820 | C | CT | 137 | a0001c0001t0004g0315 a0001c0001t0007g0149 a0001c0001t0007g0152 others(134): Show |
140 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.126+18340dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146820 | |||||||
chr3:57146820 | C | CTT | 12 | a0001c0001t0020g0022 a0001c0006t0011g0010 a0002c0003t0002g0206 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+18339_126+1834 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146820 | |||||||
chr3:57146887 | G | GC | 44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+18273_126+1827 others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146887 | |||||||
chr3:57146890 | T | TGCCATTG others(9): Show |
44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+18270_126+1827 others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146890 | |||||||
chr3:57146989 | A | AT | 10 | a0001c0001t0003g0104 a0001c0001t0003g0227 a0001c0001t0003g0228 others(7): Show |
10 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+18171dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | |||||||
chr3:57146989 | AT | A | 135 | a0001c0001t0003g0334 a0001c0001t0020g0022 a0001c0001t0020g0212 others(132): Show |
138 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.126+18171delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | |||||||
chr3:57146989 | ATT | A | 31 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0052g0299 others(28): Show |
31 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.126+18170_126+1817 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | |||||||
chr3:57146989 | ATTT | A | 6 | a0005c0005t0010g0061 a0005c0005t0010g0062 a0005c0005t0010g0090 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+18169_126+1817 others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | |||||||
chr3:57147182 | C | T | 2 | a0001c0001t0044g0194 a0001c0001t0045g0193 |
2 | NA18947.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.126+17979G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147182 | |||||||
chr3:57147313 | A | C | 4 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0060 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+17848T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147313 | |||||||
chr3:57147603 | T | C | 131 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0020g0022 others(128): Show |
132 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.126+17558A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147603 | |||||||
chr3:57147729 | T | C | 35 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(32): Show |
35 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+17432A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147729 | |||||||
chr3:57147776 | A | G | 3 | a0003c0002t0001g0219 a0003c0002t0015g0220 a0003c0002t0015g0290 |
3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+17385T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147776 | |||||||
chr3:57147781 | T | TA | 44 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(41): Show |
44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+17379dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147781 | |||||||
chr3:57148044 | C | T | 26 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.126+17117G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148044 | |||||||
chr3:57148088 | T | TG | 55 | a0001c0001t0003g0104 a0001c0001t0003g0107 a0001c0001t0003g0187 others(52): Show |
56 | HG00280.hp2 HG01069.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.126+17072dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148088 | |||||||
chr3:57148088 | TG | T | 66 | a0001c0001t0003g0043 a0001c0001t0003g0281 a0001c0001t0003g0291 others(63): Show |
68 | HG00099.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.126+17072delC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148088 | |||||||
chr3:57148088 | TGG | T | 28 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0236 others(25): Show |
31 | HG01071.hp1 HG01256.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.126+17071_126+1707 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148088 | |||||||
chr3:57148092 | G | A | 1 | a0001c0001t0043g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.126+17069C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148092 | |||||||
chr3:57148092 | G | T | 3 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 |
3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.126+17069C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148092 | |||||||
chr3:57148098 | G | A | 33 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(30): Show |
35 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+17063C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148098 | |||||||
chr3:57148099 | G | C | 1 | a0003c0002t0001g0089 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.126+17062C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148099 | |||||||
chr3:57148102 | G | A | 1 | a0005c0005t0010g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+17059C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148102 | |||||||
chr3:57148102 | G | GA | 5 | a0003c0002t0001g0147 a0003c0002t0001g0219 a0003c0002t0015g0220 others(2): Show |
5 | HG01169.hp2 HG02055.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+17058_126+1705 others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148102 | |||||||
chr3:57148104 | G | C | 61 | a0001c0001t0006g0263 a0001c0001t0042g0019 a0002c0003t0002g0002 others(58): Show |
63 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.126+17057C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148104 | |||||||
chr3:57148104 | G | GAGC | 17 | a0001c0001t0020g0212 a0003c0002t0001g0018 a0003c0002t0001g0024 others(14): Show |
17 | HG01069.hp1 HG01074.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.126+17056_126+1705 others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148104 | |||||||
chr3:57148104 | G | GGAGC | 45 | a0001c0001t0020g0022 a0002c0003t0002g0086 a0002c0003t0002g0088 others(42): Show |
46 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.126+17056_126+1705 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148104 | |||||||
chr3:57148105 | C | T | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+17056G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148105 | |||||||
chr3:57148106 | G | A | 6 | a0001c0001t0007g0003 a0001c0001t0007g0032 a0001c0001t0007g0151 others(3): Show |
7 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+17055C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148106 | |||||||
chr3:57148210 | A | C | 2 | a0003c0002t0001g0029 a0003c0002t0001g0089 |
2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.126+16951T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148210 | |||||||
chr3:57148240 | G | A | 4 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0334 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+16921C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148240 | |||||||
chr3:57148278 | T | G | 27 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(24): Show |
29 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+16883A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148278 | |||||||
chr3:57148294 | C | A | 47 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(44): Show |
47 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.126+16867G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148294 | |||||||
chr3:57148324 | C | CA | 47 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0026g0267 others(44): Show |
47 | HG01069.hp2 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.126+16836dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148324 | |||||||
chr3:57148340 | A | T | 1 | a0003c0002t0001g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+16821T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148340 | |||||||
chr3:57148378 | C | G | 47 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0027g0167 others(44): Show |
47 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.126+16783G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148378 | |||||||
chr3:57148468 | T | C | 88 | a0001c0001t0007g0121 a0001c0001t0020g0022 a0001c0001t0020g0212 others(85): Show |
89 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.126+16693A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148468 | |||||||
chr3:57148635 | G | A | 87 | a0001c0001t0020g0022 a0001c0001t0020g0212 a0002c0003t0002g0086 others(84): Show |
88 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.126+16526C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148635 | |||||||
chr3:57148677 | G | A | 1 | a0001c0001t0005g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.126+16484C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148677 | |||||||
chr3:57149227 | T | C | 7 | a0002c0003t0002g0002 a0002c0003t0002g0301 a0002c0003t0002g0302 others(4): Show |
9 | HG00558.hp2 NA18946.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15934A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149227 | |||||||
chr3:57149296 | C | CA | 34 | a0001c0001t0003g0270 a0001c0001t0004g0315 a0001c0001t0039g0268 others(31): Show |
34 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.126+15864dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149296 | |||||||
chr3:57149296 | C | CAA | 9 | a0001c0001t0003g0111 a0004c0008t0006g0044 a0004c0008t0006g0110 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15863_126+1586 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149296 | |||||||
chr3:57149296 | CA | C | 26 | a0001c0001t0006g0222 a0002c0003t0002g0002 a0002c0003t0002g0037 others(23): Show |
28 | HG00558.hp2 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+15864delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149296 | |||||||
chr3:57149318 | T | G | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+15843A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149318 | |||||||
chr3:57149399 | T | C | 9 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15762A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149399 | |||||||
chr3:57149458 | C | T | 9 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15703G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149458 | |||||||
chr3:57149559 | G | A | 9 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15602C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149559 | |||||||
chr3:57149735 | G | A | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+15426C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149735 | |||||||
chr3:57149849 | T | C | 166 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0001c0001t0007g0121 others(163): Show |
169 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.126+15312A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149849 | |||||||
chr3:57149930 | G | C | 5 | a0002c0003t0002g0093 a0002c0003t0012g0034 a0002c0003t0012g0059 others(2): Show |
5 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+15231C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149930 | |||||||
chr3:57150013 | A | C | 4 | a0002c0004t0019g0006 a0002c0004t0019g0007 a0002c0004t0048g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+15148T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150013 | |||||||
chr3:57150173 | C | T | 1 | a0001c0001t0034g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+14988G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150173 | |||||||
chr3:57150273 | G | A | 5 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0310 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+14888C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150273 | |||||||
chr3:57150302 | C | G | 1 | a0003c0002t0023g0005 | 2 | NA18993.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.126+14859G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150302 | |||||||
chr3:57150364 | C | A | 27 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(24): Show |
29 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+14797G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150364 | |||||||
chr3:57150370 | C | T | 3 | a0001c0001t0052g0299 a0002c0003t0012g0221 a0002c0004t0050g0314 |
3 | HG01243.hp1 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126+14791G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150370 | |||||||
chr3:57150437 | C | T | 6 | a0005c0005t0010g0061 a0005c0005t0010g0062 a0005c0005t0010g0090 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+14724G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150437 | |||||||
chr3:57151561 | T | A | 1 | a0002c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.126+13600A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151561 | |||||||
chr3:57151631 | A | G | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126+13530T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151631 | |||||||
chr3:57151755 | T | C | 28 | a0002c0003t0002g0002 a0002c0003t0002g0037 a0002c0003t0002g0038 others(25): Show |
30 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+13406A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151755 | |||||||
chr3:57151785 | C | T | 1 | a0002c0003t0002g0088 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.126+13376G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151785 | |||||||
chr3:57151821 | C | G | 1 | a0002c0004t0048g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126+13340G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151821 | |||||||
chr3:57151822 | A | G | 3 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0229 |
3 | HG00099.hp2 HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.126+13339T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151822 | |||||||
chr3:57151923 | A | C | 26 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(23): Show |
26 | HG01109.hp1 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.126+13238T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151923 | |||||||
chr3:57151990 | C | G | 3 | a0003c0002t0001g0219 a0003c0002t0015g0220 a0003c0002t0015g0290 |
3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+13171G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151990 | |||||||
chr3:57152007 | A | C | 161 | a0001c0001t0004g0223 a0001c0001t0004g0224 a0001c0001t0004g0226 others(158): Show |
165 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.126+13154T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152007 | |||||||
chr3:57152129 | A | C | 5 | a0003c0002t0001g0047 a0003c0002t0001g0080 a0003c0002t0001g0144 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+13032T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152129 | |||||||
chr3:57152131 | A | G | 117 | a0001c0001t0004g0112 a0001c0001t0004g0275 a0001c0001t0004g0315 others(114): Show |
118 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.126+13030T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152131 | |||||||
chr3:57152156 | G | A | 1 | a0002c0003t0012g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+13005C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152156 | |||||||
chr3:57152196 | G | C | 104 | a0001c0001t0004g0112 a0001c0001t0004g0275 a0001c0001t0005g0017 others(101): Show |
105 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.126+12965C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152196 | |||||||
chr3:57152236 | C | A | 2 | a0003c0002t0001g0047 a0003c0002t0001g0080 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.126+12925G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152236 | |||||||
chr3:57152260 | C | T | 1 | a0002c0003t0002g0098 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.126+12901G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152260 | |||||||
chr3:57152291 | A | G | 1 | a0001c0001t0003g0334 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+12870T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152291 | |||||||
chr3:57152303 | G | A | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+12858C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152303 | |||||||
chr3:57152305 | T | C | 1 | a0002c0003t0021g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.126+12856A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152305 | |||||||
chr3:57152334 | A | G | 3 | a0003c0002t0001g0219 a0003c0002t0015g0220 a0003c0002t0015g0290 |
3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+12827T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152334 | |||||||
chr3:57152372 | A | G | 1 | a0002c0012t0002g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.126+12789T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152372 | |||||||
chr3:57152433 | C | A | 1 | a0002c0003t0002g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.126+12728G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152433 | |||||||
chr3:57152552 | A | C | 70 | a0001c0001t0003g0307 a0001c0001t0004g0004 a0001c0001t0004g0190 others(67): Show |
74 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.126+12609T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152552 | |||||||
chr3:57152567 | T | G | 1 | a0002c0004t0008g0322 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+12594A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152567 | |||||||
chr3:57152759 | G | A | 6 | a0001c0006t0011g0010 a0001c0006t0011g0011 a0001c0006t0011g0012 others(3): Show |
6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+12402C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152759 | |||||||
chr3:57152762 | C | T | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.126+12399G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152762 | |||||||
chr3:57152810 | A | G | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+12351T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152810 | |||||||
chr3:57152928 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.126+12233G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152928 | |||||||
chr3:57153008 | A | G | 75 | a0001c0001t0004g0112 a0001c0001t0007g0121 a0001c0001t0035g0124 others(72): Show |
76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+12153T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153008 | |||||||
chr3:57153021 | T | C | 2 | a0003c0002t0001g0029 a0003c0002t0001g0089 |
2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.126+12140A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153021 | |||||||
chr3:57153050 | T | C | 130 | a0001c0001t0003g0111 a0001c0001t0004g0112 a0001c0001t0004g0184 others(127): Show |
131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+12111A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153050 | |||||||
chr3:57153329 | A | C | 1 | a0001c0001t0004g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.126+11832T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153329 | |||||||
chr3:57153468 | G | A | 26 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0002g0300 others(23): Show |
26 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+11693C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153468 | |||||||
chr3:57153532 | A | G | 1 | a0003c0002t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+11629T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153532 | |||||||
chr3:57153789 | G | A | 2 | a0001c0001t0038g0035 a0002c0003t0013g0063 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.126+11372C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153789 | |||||||
chr3:57153812 | C | T | 1 | a0001c0001t0007g0121 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+11349G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153812 | |||||||
chr3:57153913 | G | A | 1 | a0002c0003t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126+11248C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153913 | |||||||
chr3:57154052 | C | T | 1 | a0001c0001t0004g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.126+11109G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154052 | |||||||
chr3:57154259 | A | T | 2 | a0001c0001t0018g0331 a0006c0014t0018g0330 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.126+10902T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154259 | |||||||
chr3:57154260 | T | TTA | 29 | a0001c0001t0003g0043 a0001c0001t0003g0107 a0001c0001t0003g0281 others(26): Show |
29 | HG00099.hp1 HG00609.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+10899_126+1090 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | |||||||
chr3:57154260 | T | TTATA | 3 | a0001c0001t0005g0214 a0001c0001t0027g0167 a0002c0004t0008g0215 |
3 | HG01346.hp2 HG03130.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.126+10897_126+1090 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | |||||||
chr3:57154260 | T | TTATATAT others(5): Show |
2 | a0002c0004t0019g0006 a0002c0004t0048g0008 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.126+10889_126+1090 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | |||||||
chr3:57154260 | T | TTATATAT others(7): Show |
2 | a0002c0004t0019g0007 a0002c0004t0051g0020 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.126+10887_126+1090 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | |||||||
chr3:57154260 | TTA | T | 14 | a0001c0001t0004g0184 a0002c0003t0002g0093 a0002c0003t0012g0034 others(11): Show |
14 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+10899_126+1090 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | |||||||
chr3:57154279 | T | TACACACA others(13): Show |
2 | a0002c0003t0013g0324 a0002c0003t0014g0323 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.126+10881_126+1088 others(24): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | |||||||
chr3:57154279 | T | TACACACA others(15): Show |
2 | a0001c0001t0004g0315 a0002c0003t0013g0078 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.126+10881_126+1088 others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | |||||||
chr3:57154279 | T | TACACACA others(17): Show |
3 | a0002c0003t0013g0325 a0002c0003t0013g0326 a0002c0003t0021g0340 |
3 | HG02970.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.126+10881_126+1088 others(28): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | |||||||
chr3:57154279 | TATATACA others(5): Show |
T | 2 | a0003c0002t0001g0118 a0003c0002t0001g0119 |
2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+10870_126+1088 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | |||||||
chr3:57154281 | T | C | 7 | a0001c0001t0004g0315 a0002c0003t0013g0078 a0002c0003t0013g0324 others(4): Show |
7 | HG02622.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+10880A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154281 | |||||||
chr3:57154281 | TATACACA others(3): Show |
T | 71 | a0001c0001t0004g0112 a0001c0001t0007g0121 a0001c0001t0035g0124 others(68): Show |
72 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.126+10870_126+1087 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154281 | |||||||
chr3:57154283 | T | C | 9 | a0001c0001t0004g0315 a0002c0003t0013g0078 a0002c0003t0013g0324 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+10878A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TAC | 5 | a0002c0003t0002g0243 a0002c0003t0002g0269 a0002c0003t0022g0097 others(2): Show |
5 | HG02622.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+10876_126+1087 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TACACATA others(9): Show |
3 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 |
3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TATACACA others(11): Show |
3 | a0001c0001t0003g0111 a0004c0008t0006g0044 a0004c0008t0006g0110 |
3 | HG01243.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TATACACA others(11): Show |
1 | a0002c0004t0008g0322 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TATATACA others(9): Show |
4 | a0002c0007t0009g0075 a0002c0007t0009g0310 a0002c0007t0009g0311 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+10877_126+1087 others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TATATACA others(11): Show |
1 | a0004c0008t0006g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TATATATA others(11): Show |
3 | a0002c0003t0055g0009 a0002c0007t0009g0074 a0004c0008t0006g0313 |
3 | HG02109.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TATATATA others(21): Show |
2 | a0002c0004t0016g0341 a0002c0004t0016g0342 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(32): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154283 | T | TATATATA others(33): Show |
1 | a0002c0003t0002g0300 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.126+10877_126+1087 others(44): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | |||||||
chr3:57154285 | C | T | 18 | a0001c0001t0038g0035 a0001c0001t0046g0309 a0001c0006t0011g0010 others(15): Show |
18 | HG01109.hp1 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+10876G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154285 | |||||||
chr3:57154287 | C | T | 1 | a0002c0004t0019g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.126+10874G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154287 | |||||||
chr3:57154303 | T | C | 12 | a0001c0001t0003g0111 a0002c0003t0002g0300 a0002c0003t0055g0009 others(9): Show |
12 | HG01243.hp2 HG02109.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+10858A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154303 | |||||||
chr3:57154418 | T | TGC | 75 | a0001c0001t0004g0112 a0001c0001t0007g0121 a0001c0001t0035g0124 others(72): Show |
76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+10741_126+1074 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154418 | |||||||
chr3:57154649 | T | C | 15 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(12): Show |
15 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+10512A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154649 | |||||||
chr3:57154725 | A | C | 1 | a0003c0011t0001g0122 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.126+10436T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154725 | |||||||
chr3:57154818 | C | T | 15 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(12): Show |
15 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+10343G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154818 | |||||||
chr3:57155028 | G | C | 1 | a0002c0004t0008g0322 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+10133C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155028 | |||||||
chr3:57155030 | C | T | 2 | a0001c0001t0052g0299 a0002c0003t0012g0221 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.126+10131G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155030 | |||||||
chr3:57155058 | C | T | 1 | a0002c0004t0051g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+10103G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155058 | |||||||
chr3:57155195 | A | G | 3 | a0003c0002t0001g0219 a0003c0002t0015g0220 a0003c0002t0015g0290 |
3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+9966T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155195 | |||||||
chr3:57155281 | G | A | 2 | a0002c0004t0016g0341 a0002c0004t0016g0342 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+9880C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155281 | |||||||
chr3:57155611 | G | T | 2 | a0002c0003t0002g0217 a0003c0002t0001g0218 |
2 | NA18978.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.126+9550C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155611 | |||||||
chr3:57155792 | T | C | 2 | a0002c0004t0049g0168 a0003c0002t0001g0169 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.126+9369A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155792 | |||||||
chr3:57155896 | G | A | 6 | a0001c0006t0011g0010 a0001c0006t0011g0011 a0001c0006t0011g0012 others(3): Show |
6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+9265C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155896 | |||||||
chr3:57155898 | A | G | 1 | a0001c0001t0033g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.126+9263T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155898 | |||||||
chr3:57155956 | T | C | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+9205A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155956 | |||||||
chr3:57156178 | A | G | 6 | a0001c0006t0011g0010 a0001c0006t0011g0011 a0001c0006t0011g0012 others(3): Show |
6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+8983T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156178 | |||||||
chr3:57156183 | G | T | 130 | a0001c0001t0003g0111 a0001c0001t0004g0112 a0001c0001t0004g0184 others(127): Show |
131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+8978C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156183 | |||||||
chr3:57156191 | A | G | 6 | a0001c0006t0011g0010 a0001c0006t0011g0011 a0001c0006t0011g0012 others(3): Show |
6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+8970T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156191 | |||||||
chr3:57156218 | A | G | 1 | a0001c0001t0004g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.126+8943T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156218 | |||||||
chr3:57156275 | C | CTT | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+8885_126+8886i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156275 | |||||||
chr3:57156424 | A | G | 130 | a0001c0001t0003g0111 a0001c0001t0004g0112 a0001c0001t0004g0184 others(127): Show |
131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+8737T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156424 | |||||||
chr3:57156557 | C | T | 11 | a0001c0001t0007g0003 a0001c0001t0007g0031 a0001c0001t0007g0032 others(8): Show |
12 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+8604G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156557 | |||||||
chr3:57156582 | T | G | 1 | a0003c0002t0001g0030 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.126+8579A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156582 | |||||||
chr3:57156669 | C | T | 1 | a0002c0003t0002g0301 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.126+8492G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156669 | |||||||
chr3:57156777 | T | C | 14 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0001c0006t0011g0010 others(11): Show |
14 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+8384A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156777 | |||||||
chr3:57156783 | G | C | 134 | a0001c0001t0003g0111 a0001c0001t0004g0112 a0001c0001t0004g0184 others(131): Show |
135 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.126+8378C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156783 | |||||||
chr3:57156796 | C | T | 1 | a0001c0001t0007g0121 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+8365G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156796 | |||||||
chr3:57156844 | C | G | 5 | a0001c0001t0018g0331 a0002c0003t0022g0097 a0002c0003t0022g0216 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+8317G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156844 | |||||||
chr3:57156847 | C | T | 1 | a0001c0001t0037g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.126+8314G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156847 | |||||||
chr3:57156887 | C | T | 2 | a0003c0002t0001g0047 a0003c0002t0001g0080 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.126+8274G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156887 | |||||||
chr3:57157077 | T | C | 1 | a0003c0002t0001g0116 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.126+8084A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157077 | |||||||
chr3:57157287 | A | G | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7874T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157287 | |||||||
chr3:57157288 | A | T | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7873T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157288 | |||||||
chr3:57157533 | A | G | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7628T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157533 | |||||||
chr3:57157617 | C | T | 2 | a0001c0001t0004g0045 a0001c0001t0037g0041 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.126+7544G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157617 | |||||||
chr3:57157644 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126+7517G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157644 | |||||||
chr3:57157648 | G | A | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+7513C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157648 | |||||||
chr3:57157810 | C | G | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+7351G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157810 | |||||||
chr3:57157812 | A | T | 1 | a0001c0001t0005g0160 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.126+7349T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157812 | |||||||
chr3:57157830 | C | T | 1 | a0003c0002t0001g0079 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.126+7331G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157830 | |||||||
chr3:57157850 | C | T | 75 | a0001c0001t0004g0112 a0001c0001t0007g0121 a0001c0001t0035g0124 others(72): Show |
76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+7311G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157850 | |||||||
chr3:57157867 | C | T | 75 | a0001c0001t0004g0112 a0001c0001t0007g0121 a0001c0001t0035g0124 others(72): Show |
76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+7294G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157867 | |||||||
chr3:57158016 | G | A | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7145C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158016 | |||||||
chr3:57158018 | T | C | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7143A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158018 | |||||||
chr3:57158072 | T | C | 1 | a0003c0002t0001g0058 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.126+7089A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158072 | |||||||
chr3:57158197 | A | G | 2 | a0001c0001t0018g0331 a0006c0014t0018g0330 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.126+6964T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158197 | |||||||
chr3:57158266 | G | T | 81 | a0001c0001t0003g0307 a0001c0001t0004g0004 a0001c0001t0004g0190 others(78): Show |
85 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.126+6895C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158266 | |||||||
chr3:57158380 | T | C | 1 | a0002c0004t0057g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+6781A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158380 | |||||||
chr3:57158512 | G | A | 4 | a0001c0001t0003g0336 a0002c0003t0002g0073 a0002c0003t0002g0155 others(1): Show |
4 | NA18961.hp1 NA18982.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+6649C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158512 | |||||||
chr3:57158548 | A | G | 1 | a0002c0003t0002g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.126+6613T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158548 | |||||||
chr3:57158560 | C | A | 1 | a0001c0001t0003g0289 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.126+6601G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158560 | |||||||
chr3:57158693 | G | T | 2 | a0003c0002t0001g0016 a0003c0002t0001g0120 |
2 | NA18956.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.126+6468C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158693 | |||||||
chr3:57158766 | T | C | 2 | a0003c0002t0001g0118 a0003c0002t0001g0119 |
2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+6395A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158766 | |||||||
chr3:57158791 | A | G | 1 | a0001c0001t0052g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126+6370T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158791 | |||||||
chr3:57158868 | C | T | 6 | a0002c0003t0013g0078 a0002c0003t0013g0324 a0002c0003t0013g0325 others(3): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+6293G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158868 | |||||||
chr3:57158899 | A | G | 75 | a0001c0001t0004g0112 a0001c0001t0007g0121 a0001c0001t0035g0124 others(72): Show |
76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+6262T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158899 | |||||||
chr3:57158972 | G | C | 2 | a0003c0002t0001g0118 a0003c0002t0001g0119 |
2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+6189C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158972 | |||||||
chr3:57159054 | T | C | 4 | a0002c0004t0019g0006 a0002c0004t0019g0007 a0002c0004t0048g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+6107A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159054 | |||||||
chr3:57159112 | C | T | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+6049G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159112 | |||||||
chr3:57159123 | CT | C | 126 | a0001c0001t0003g0111 a0001c0001t0003g0291 a0001c0001t0003g0293 others(123): Show |
127 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.126+6037delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159123 | |||||||
chr3:57159474 | C | T | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+5687G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159474 | |||||||
chr3:57159487 | T | A | 4 | a0002c0004t0008g0298 a0003c0002t0001g0295 a0003c0002t0001g0296 others(1): Show |
4 | HG00099.hp1 HG01496.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+5674A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159487 | |||||||
chr3:57159526 | G | A | 5 | a0001c0001t0038g0035 a0002c0003t0013g0063 a0002c0003t0014g0170 others(2): Show |
5 | HG01109.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5635C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159526 | |||||||
chr3:57159549 | C | T | 2 | a0001c0001t0003g0186 a0001c0001t0003g0187 |
2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.126+5612G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159549 | |||||||
chr3:57159641 | G | GC | 10 | a0001c0001t0003g0111 a0002c0007t0009g0074 a0002c0007t0009g0075 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+5519dupG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159641 | |||||||
chr3:57159695 | TG | T | 5 | a0002c0007t0009g0074 a0002c0007t0009g0075 a0002c0007t0009g0310 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5465delC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159695 | |||||||
chr3:57159735 | G | C | 1 | a0001c0001t0005g0017 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+5426C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159735 | |||||||
chr3:57159863 | C | CAG | 11 | a0001c0001t0003g0111 a0002c0003t0055g0009 a0002c0007t0009g0074 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+5296_126+5297d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159863 | |||||||
chr3:57160244 | C | T | 130 | a0001c0001t0003g0111 a0001c0001t0004g0112 a0001c0001t0004g0184 others(127): Show |
131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+4917G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160244 | |||||||
chr3:57160312 | G | GA | 8 | a0001c0001t0007g0003 a0001c0001t0007g0032 a0001c0001t0007g0046 others(5): Show |
9 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+4848dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160312 | |||||||
chr3:57160312 | G | GAA | 22 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0002g0300 others(19): Show |
22 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.126+4847_126+4848d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160312 | |||||||
chr3:57160398 | G | T | 75 | a0001c0001t0004g0112 a0001c0001t0007g0121 a0001c0001t0035g0124 others(72): Show |
76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+4763C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160398 | |||||||
chr3:57160489 | A | C | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+4672T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160489 | |||||||
chr3:57160552 | T | A | 1 | a0002c0003t0002g0300 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.126+4609A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160552 | |||||||
chr3:57160642 | T | C | 2 | a0001c0001t0018g0331 a0006c0014t0018g0330 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.126+4519A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160642 | |||||||
chr3:57160763 | A | G | 1 | a0001c0001t0005g0033 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.126+4398T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160763 | |||||||
chr3:57160806 | A | G | 1 | a0003c0002t0001g0173 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.126+4355T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160806 | |||||||
chr3:57160935 | A | G | 3 | a0003c0002t0001g0117 a0003c0002t0001g0118 a0003c0002t0001g0119 |
3 | HG02735.hp2 NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+4226T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160935 | |||||||
chr3:57161015 | C | T | 1 | a0003c0002t0001g0116 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.126+4146G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161015 | |||||||
chr3:57161034 | C | G | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+4127G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161034 | |||||||
chr3:57161248 | C | G | 25 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0013g0078 others(22): Show |
25 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+3913G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161248 | |||||||
chr3:57161339 | C | T | 1 | a0002c0004t0050g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+3822G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161339 | |||||||
chr3:57161446 | A | G | 8 | a0001c0001t0027g0167 a0001c0001t0038g0035 a0002c0003t0013g0063 others(5): Show |
8 | HG01109.hp1 HG01109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+3715T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161446 | |||||||
chr3:57161514 | C | T | 1 | a0003c0002t0001g0166 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.126+3647G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161514 | |||||||
chr3:57161647 | G | C | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+3514C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161647 | |||||||
chr3:57161764 | G | A | 2 | a0001c0001t0005g0001 a0001c0001t0028g0109 |
4 | NA18941.hp2 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3397C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161764 | |||||||
chr3:57161840 | GGT | G | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+3319_126+3320d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161840 | |||||||
chr3:57161982 | A | C | 1 | a0002c0003t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126+3179T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161982 | |||||||
chr3:57162022 | T | C | 8 | a0001c0001t0003g0307 a0002c0003t0002g0002 a0002c0003t0002g0301 others(5): Show |
10 | HG00558.hp2 NA18946.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+3139A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162022 | |||||||
chr3:57162142 | T | C | 25 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0013g0078 others(22): Show |
25 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+3019A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162142 | |||||||
chr3:57162209 | G | C | 25 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0013g0078 others(22): Show |
25 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+2952C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162209 | |||||||
chr3:57162230 | T | C | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2931A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162230 | |||||||
chr3:57162335 | C | T | 1 | a0001c0001t0007g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.126+2826G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162335 | |||||||
chr3:57162356 | A | G | 7 | a0001c0001t0005g0017 a0001c0001t0005g0160 a0001c0001t0005g0161 others(4): Show |
7 | HG00642.hp1 HG01106.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+2805T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162356 | |||||||
chr3:57162361 | C | T | 3 | a0002c0003t0012g0034 a0002c0003t0012g0059 a0002c0003t0012g0156 |
3 | HG01255.hp1 HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.126+2800G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162361 | |||||||
chr3:57162378 | T | C | 1 | a0001c0001t0003g0334 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+2783A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162378 | |||||||
chr3:57162383 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+2778G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162383 | |||||||
chr3:57162608 | C | T | 11 | a0001c0006t0011g0158 a0002c0003t0012g0034 a0002c0003t0012g0059 others(8): Show |
11 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+2553G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162608 | |||||||
chr3:57162811 | T | C | 1 | a0002c0003t0002g0308 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.126+2350A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162811 | |||||||
chr3:57162820 | A | G | 75 | a0001c0001t0005g0033 a0001c0001t0007g0003 a0001c0001t0007g0031 others(72): Show |
76 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+2341T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162820 | |||||||
chr3:57162882 | G | A | 1 | a0001c0001t0046g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.126+2279C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162882 | |||||||
chr3:57162983 | G | C | 1 | a0002c0004t0008g0322 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+2178C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162983 | |||||||
chr3:57162990 | G | A | 21 | a0001c0001t0003g0111 a0001c0001t0004g0315 a0002c0003t0013g0078 others(18): Show |
21 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.126+2171C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162990 | |||||||
chr3:57163090 | G | A | 2 | a0001c0001t0004g0315 a0002c0004t0050g0314 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.126+2071C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163090 | |||||||
chr3:57163142 | G | A | 1 | a0001c0001t0004g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.126+2019C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163142 | |||||||
chr3:57163223 | C | G | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1938G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163223 | |||||||
chr3:57163246 | C | G | 4 | a0002c0004t0008g0077 a0002c0004t0008g0320 a0002c0004t0008g0321 others(1): Show |
4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1915G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163246 | |||||||
chr3:57163246 | C | T | 75 | a0001c0001t0007g0003 a0001c0001t0007g0031 a0001c0001t0007g0032 others(72): Show |
76 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+1915G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163246 | |||||||
chr3:57163255 | G | A | 1 | a0002c0003t0002g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.126+1906C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163255 | |||||||
chr3:57163300 | C | G | 2 | a0002c0003t0002g0114 a0002c0003t0002g0115 |
2 | NA19056.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.126+1861G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163300 | |||||||
chr3:57163426 | G | A | 3 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0319 |
3 | HG02258.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.126+1735C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163426 | |||||||
chr3:57163446 | C | T | 1 | a0004c0008t0006g0113 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.126+1715G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163446 | |||||||
chr3:57163467 | G | C | 1 | a0001c0001t0018g0331 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.126+1694C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163467 | |||||||
chr3:57163521 | C | A | 11 | a0001c0001t0004g0112 a0002c0003t0013g0078 a0002c0003t0013g0324 others(8): Show |
11 | HG00639.hp1 HG02622.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+1640G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163521 | |||||||
chr3:57163542 | T | A | 3 | a0001c0001t0005g0327 a0001c0001t0005g0328 a0001c0001t0005g0329 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.126+1619A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163542 | |||||||
chr3:57163555 | C | A | 1 | a0001c0001t0003g0015 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.126+1606G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163555 | |||||||
chr3:57163785 | C | CG | 37 | a0001c0001t0003g0104 a0001c0001t0003g0107 a0001c0001t0003g0111 others(34): Show |
37 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.126+1375dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163785 | |||||||
chr3:57163785 | C | CGG | 33 | a0001c0001t0007g0046 a0001c0001t0033g0071 a0002c0003t0002g0048 others(30): Show |
33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.126+1374_126+1375d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163785 | |||||||
chr3:57163785 | C | CGGG | 24 | a0001c0001t0003g0043 a0001c0001t0004g0045 a0001c0001t0005g0033 others(21): Show |
24 | HG00280.hp2 HG01123.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+1373_126+1375d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163785 | |||||||
chr3:57163792 | GC | G | 9 | a0001c0001t0003g0265 a0001c0001t0003g0289 a0001c0001t0004g0319 others(6): Show |
9 | HG00639.hp1 HG02647.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+1368delG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163792 | |||||||
chr3:57163793 | C | CG | 28 | a0001c0001t0003g0253 a0001c0001t0003g0307 a0001c0001t0004g0210 others(25): Show |
29 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+1367dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163793 | |||||||
chr3:57163793 | C | G | 148 | a0001c0001t0003g0043 a0001c0001t0003g0111 a0001c0001t0003g0266 others(145): Show |
149 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(146): Show |
intron_variant | MODIFIER | c.126+1368G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163793 | |||||||
chr3:57163794 | G | C | 1 | a0002c0003t0021g0340 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+1367C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163794 | |||||||
chr3:57163800 | G | A | 3 | a0001c0001t0018g0331 a0002c0003t0021g0340 a0006c0014t0018g0330 |
3 | HG02486.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.126+1361C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163800 | |||||||
chr3:57163803 | A | AG | 5 | a0001c0001t0005g0161 a0002c0003t0002g0098 a0003c0002t0001g0147 others(2): Show |
5 | HG00673.hp1 HG01358.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+1357dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163803 | |||||||
chr3:57163803 | A | G | 12 | a0001c0001t0004g0240 a0001c0001t0007g0151 a0001c0001t0007g0152 others(9): Show |
12 | HG01106.hp2 HG01255.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+1358T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163803 | |||||||
chr3:57163808 | GT | G | 8 | a0001c0001t0003g0334 a0001c0006t0011g0010 a0001c0006t0011g0011 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+1352delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163808 | |||||||
chr3:57163809 | T | G | 3 | a0001c0001t0004g0315 a0001c0001t0027g0167 a0002c0003t0021g0279 |
3 | HG01934.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.126+1352A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163809 | |||||||
chr3:57163843 | G | A | 1 | a0002c0003t0002g0335 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.126+1318C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163843 | |||||||
chr3:57163910 | C | T | 1 | a0001c0001t0020g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.126+1251G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163910 | |||||||
chr3:57164039 | T | C | 1 | a0001c0001t0003g0336 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.126+1122A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164039 | |||||||
chr3:57164092 | A | C | 3 | a0002c0003t0054g0021 a0002c0004t0016g0341 a0002c0004t0016g0342 |
3 | HG02257.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.126+1069T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164092 | |||||||
chr3:57164190 | C | T | 1 | a0002c0004t0051g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+971G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164190 | |||||||
chr3:57164215 | C | T | 1 | a0001c0001t0042g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.126+946G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164215 | |||||||
chr3:57164234 | G | T | 1 | a0003c0002t0001g0018 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.126+927C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164234 | |||||||
chr3:57164336 | G | C | 3 | a0002c0003t0002g0337 a0002c0003t0002g0338 a0002c0003t0002g0339 |
3 | NA18974.hp1 NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.126+825C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164336 | |||||||
chr3:57164717 | A | T | 1 | a0001c0001t0005g0017 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+444T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164717 | |||||||
chr3:57164769 | C | T | 1 | a0003c0002t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.126+392G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164769 | |||||||
chr3:57164775 | C | A | 1 | a0002c0003t0021g0340 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+386G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164775 | |||||||
chr3:57164940 | A | G | 1 | a0001c0001t0003g0015 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.126+221T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164940 | |||||||
chr3:57165051 | C | T | 2 | a0002c0004t0016g0341 a0002c0004t0016g0342 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+110G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57165051 | |||||||
chr3:57165110 | T | C | 2 | a0002c0004t0016g0341 a0002c0004t0016g0342 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+51A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57165110 | |||||||
chr3:57165115 | C | T | 9 | a0001c0006t0011g0010 a0001c0006t0011g0011 a0001c0006t0011g0012 others(6): Show |
9 | HG01884.hp2 HG02145.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+46G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57165115 |