Item | Value |
---|---|
geneid | 9742 |
ensemblid | ENSG00000187535.14 |
hgncid | 29077 |
symbol | IFT140 |
name | intraflagellar transport 140 |
refseq_nuc | NM_014714.4 |
refseq_prot | NP_055529.2 |
ensembl_nuc | ENST00000426508.7 |
ensembl_prot | ENSP00000406012.2 |
mane_status | MANE Select |
chr | chr16 |
start | 1510427 |
end | 1612072 |
strand | - |
ver | v1.2 |
region | chr16:1510427-1612072 |
region5000 | chr16:1505427-1617072 |
regionname0 | IFT140_chr16_1510427_1612072 |
regionname5000 | IFT140_chr16_1505427_1617072 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1462 | 212 | 54 | 31 | 87 | 6 | 32 | 60 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0002 | 0/0 | 1462 | 29 | 0 | 7 | 19 | 1 | 2 | 16 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0003 | 0/0 | 1462 | 27 | 7 | 2 | 10 | 2 | 6 | 7 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0004 | 0/0 | 1462 | 9 | 0 | 9 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0005 | 0/0 | 1462 | 8 | 6 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0006 | 0/0 | 1462 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0007 | 0/0 | 1462 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0008 | 0/0 | 1462 | 4 | 0 | 1 | 3 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0009 | 0/0 | 1462 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0010 | 0/0 | 1462 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0011 | 0/0 | 1462 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0012 | 0/0 | 1462 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0013 | 0/0 | 1462 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0014 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0015 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0016 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0017 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0018 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0019 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0020 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0021 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0022 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0023 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0024 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0025 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0026 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0027 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0028 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0029 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0030 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
a0031 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | MALYY others(1457): Show |
chr16 | 1505427 | 1617072 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4386 | 103 | 20 | 19 | 40 | 5 | 17 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0002 | 0/0 | 4386 | 64 | 23 | 7 | 20 | 1 | 13 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0004 | 0/0 | 4386 | 21 | 9 | 2 | 9 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0008 | 0/0 | 4386 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0010 | 0/0 | 4386 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0014 | 0/0 | 4386 | 3 | 0 | 0 | 3 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0020 | 0/0 | 4386 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0037 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0043 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0045 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0048 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0050 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0052 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0053 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0054 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0001c0057 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0002c0003 | 0/0 | 4386 | 29 | 0 | 7 | 19 | 1 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0003c0005 | 0/0 | 4386 | 18 | 3 | 1 | 9 | 2 | 3 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0003c0017 | 0/0 | 4386 | 2 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0003c0018 | 0/0 | 4386 | 2 | 0 | 0 | 1 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0003c0019 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0003c0031 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0003c0032 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0003c0059 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0004c0006 | 0/0 | 4386 | 7 | 0 | 7 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0004c0025 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0004c0026 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0005c0009 | 0/0 | 4386 | 5 | 4 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0005c0039 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0005c0044 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0005c0049 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0006c0007 | 0/0 | 4386 | 6 | 6 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0007c0013 | 0/0 | 4386 | 4 | 3 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0007c0060 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0008c0021 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0008c0040 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0008c0046 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0009c0011 | 0/0 | 4386 | 4 | 0 | 3 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0010c0015 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0010c0016 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0011c0012 | 0/0 | 4386 | 4 | 4 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0012c0022 | 0/0 | 4386 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0013c0023 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0014c0042 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0015c0056 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0016c0038 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0017c0055 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0018c0061 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0019c0058 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0020c0036 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0021c0047 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0022c0028 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0023c0030 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0024c0033 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0025c0024 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0026c0027 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0027c0041 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0028c0029 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0029c0051 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0030c0034 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 | ||
a0031c0035 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | ATGGC others(4381): Show |
chr16 | 1505427 | 1617072 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/1 | 5232 | 92 | 13 | 18 | 39 | 4 | 16 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0001t0003 | 0/0 | 5232 | 2 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0001t0004 | 0/0 | 5232 | 7 | 6 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0001t0007 | 0/0 | 5232 | 2 | 0 | 0 | 0 | 1 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0002t0001 | 0/0 | 5232 | 57 | 21 | 6 | 19 | 1 | 10 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0002t0003 | 0/0 | 5232 | 4 | 2 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0002t0005 | 0/0 | 5232 | 2 | 0 | 0 | 0 | 0 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0002t0010 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0004t0001 | 0/0 | 5232 | 8 | 5 | 1 | 1 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0004t0003 | 0/0 | 5232 | 13 | 4 | 1 | 8 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0008t0001 | 0/0 | 5232 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0010t0001 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0010t0002 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0010t0004 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0014t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0014t0006 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0020t0003 | 0/0 | 5232 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0037t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0043t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0045t0002 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0048t0002 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0050t0002 | 0/0 | 5232 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0052t0004 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0053t0002 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0054t0001 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0001c0057t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0002c0003t0003 | 0/0 | 5232 | 29 | 0 | 7 | 19 | 1 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0005t0001 | 0/0 | 5232 | 12 | 1 | 1 | 7 | 0 | 3 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0005t0003 | 0/0 | 5232 | 6 | 2 | 0 | 2 | 2 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0017t0001 | 0/0 | 5232 | 2 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0018t0001 | 0/0 | 5232 | 2 | 0 | 0 | 1 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0019t0003 | 0/0 | 5232 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0031t0009 | 0/0 | 5232 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0032t0008 | 0/0 | 5232 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0003c0059t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0004c0006t0002 | 0/0 | 5232 | 7 | 0 | 7 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0004c0025t0002 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0004c0026t0004 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0005c0009t0004 | 0/0 | 5232 | 5 | 4 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0005c0039t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0005c0044t0004 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0005c0049t0004 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0006c0007t0003 | 0/0 | 5232 | 6 | 6 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0007c0013t0001 | 0/0 | 5232 | 4 | 3 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0007c0060t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0008c0021t0002 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0008c0040t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0008c0046t0004 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0009c0011t0003 | 0/0 | 5232 | 4 | 0 | 3 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0010c0015t0003 | 0/0 | 5232 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0010c0016t0001 | 0/0 | 5232 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0011c0012t0003 | 0/0 | 5232 | 4 | 4 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0012c0022t0002 | 0/0 | 5232 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0013c0023t0001 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0014c0042t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0015c0056t0001 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0016c0038t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0017c0055t0004 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0018c0061t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0019c0058t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0020c0036t0003 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0021c0047t0002 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0022c0028t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0023c0030t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0024c0033t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0025c0024t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0026c0027t0003 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0027c0041t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0028c0029t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0029c0051t0004 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0030c0034t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
a0031c0035t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | GCAGC others(5227): Show |
chr16 | 1505427 | 1617072 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0284 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0001t0007g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0002t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0004t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0008t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0008t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0010t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0010t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0010t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0010t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0010t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0014t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0014t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0014t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0020t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0020t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0037t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0043t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0045t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0048t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0050t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0052t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0053t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0054t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0001c0057t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0002c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0005t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0017t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0017t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0018t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0018t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0019t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0019t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0031t0009g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0032t0008g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0003c0059t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0006t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0006t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0006t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0006t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0006t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0006t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0006t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0025t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0004c0026t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0009t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0009t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0009t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0009t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0009t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0039t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0044t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0005c0049t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0006c0007t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0006c0007t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0006c0007t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0006c0007t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0006c0007t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0006c0007t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0007c0013t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0007c0013t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0007c0013t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0007c0013t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0007c0060t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0008c0021t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0008c0021t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0008c0040t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0008c0046t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0009c0011t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0009c0011t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0009c0011t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0009c0011t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0010c0015t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0010c0015t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0010c0016t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0010c0016t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0011c0012t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0011c0012t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0011c0012t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0011c0012t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0012c0022t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0012c0022t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0013c0023t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0013c0023t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0014c0042t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0015c0056t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0016c0038t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0017c0055t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0018c0061t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0019c0058t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0020c0036t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0021c0047t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0022c0028t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0023c0030t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0024c0033t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0025c0024t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0026c0027t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0027c0041t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0028c0029t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0029c0051t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0030c0034t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
a0031c0035t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0305 | EUR | GBR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00099 | hp2 | a0003 | c0005 | t0003 | g0148 | EUR | GBR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00280 | hp1 | a0003 | c0005 | t0003 | g0153 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0070 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0270 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00408 | hp1 | a0002 | c0003 | t0003 | g0020 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00544 | hp1 | a0002 | c0003 | t0003 | g0026 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00544 | hp2 | a0001 | c0004 | t0003 | g0185 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00609 | hp1 | a0001 | c0048 | t0002 | g0256 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00609 | hp2 | a0003 | c0005 | t0003 | g0151 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00639 | hp1 | a0001 | c0054 | t0001 | g0119 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00639 | hp2 | a0001 | c0004 | t0003 | g0100 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00642 | hp1 | a0012 | c0022 | t0002 | g0231 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00642 | hp2 | a0002 | c0003 | t0003 | g0021 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00673 | hp1 | a0014 | c0042 | t0001 | g0108 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00733 | hp1 | a0004 | c0026 | t0004 | g0312 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG00741 | hp2 | a0004 | c0006 | t0002 | g0251 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01069 | hp1 | a0001 | c0020 | t0003 | g0139 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01070 | hp1 | a0005 | c0009 | t0004 | g0167 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01070 | hp2 | a0002 | c0003 | t0003 | g0028 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01071 | hp1 | a0002 | c0003 | t0003 | g0027 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01071 | hp2 | a0001 | c0020 | t0003 | g0138 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01099 | hp2 | a0012 | c0022 | t0002 | g0236 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01109 | hp2 | a0007 | c0013 | t0001 | g0191 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01175 | hp1 | a0015 | c0056 | t0001 | g0067 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01175 | hp2 | a0004 | c0006 | t0002 | g0313 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01192 | hp1 | a0003 | c0005 | t0001 | g0146 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01192 | hp2 | a0008 | c0046 | t0004 | g0258 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01243 | hp2 | a0003 | c0017 | t0001 | g0058 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01256 | hp1 | a0004 | c0006 | t0002 | g0204 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01257 | hp2 | a0009 | c0011 | t0003 | g0044 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01261 | hp1 | a0009 | c0011 | t0003 | g0042 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01261 | hp2 | a0002 | c0003 | t0003 | g0034 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01346 | hp1 | a0009 | c0011 | t0003 | g0043 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01346 | hp2 | a0004 | c0006 | t0002 | g0246 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01496 | hp1 | a0004 | c0006 | t0002 | g0243 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01516 | hp1 | a0009 | c0011 | t0003 | g0045 | EUR | IBS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0307 | EUR | IBS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01884 | hp1 | a0005 | c0009 | t0004 | g0177 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01891 | hp1 | a0007 | c0013 | t0001 | g0194 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01928 | hp1 | a0002 | c0003 | t0003 | g0016 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01978 | hp2 | a0004 | c0006 | t0002 | g0327 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01993 | hp1 | a0002 | c0003 | t0003 | g0011 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02004 | hp2 | a0004 | c0006 | t0002 | g0241 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02015 | hp1 | a0003 | c0005 | t0001 | g0155 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02015 | hp2 | a0016 | c0038 | t0001 | g0094 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02055 | hp2 | a0007 | c0060 | t0001 | g0195 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02056 | hp1 | a0001 | c0004 | t0001 | g0084 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02056 | hp2 | a0008 | c0021 | t0002 | g0316 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02071 | hp1 | a0001 | c0043 | t0001 | g0219 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02074 | hp2 | a0008 | c0021 | t0002 | g0315 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02080 | hp1 | a0001 | c0014 | t0003 | g0102 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02080 | hp2 | a0001 | c0057 | t0003 | g0214 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02083 | hp2 | a0001 | c0004 | t0003 | g0124 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02129 | hp2 | a0003 | c0005 | t0001 | g0149 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02132 | hp2 | a0001 | c0052 | t0004 | g0242 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02135 | hp1 | a0001 | c0010 | t0004 | g0238 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02145 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02148 | hp2 | a0002 | c0003 | t0003 | g0022 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02165 | hp2 | a0005 | c0039 | t0001 | g0158 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02258 | hp1 | a0017 | c0055 | t0004 | g0165 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02280 | hp2 | a0003 | c0017 | t0001 | g0059 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02523 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02523 | hp2 | a0001 | c0014 | t0006 | g0209 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02572 | hp1 | a0005 | c0044 | t0004 | g0168 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02572 | hp2 | a0007 | c0013 | t0001 | g0193 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02615 | hp1 | a0018 | c0061 | t0001 | g0116 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0105 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02630 | hp2 | a0005 | c0009 | t0004 | g0173 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02647 | hp2 | a0003 | c0005 | t0001 | g0150 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02683 | hp1 | a0001 | c0001 | t0007 | g0265 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02683 | hp2 | a0003 | c0032 | t0008 | g0003 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02809 | hp2 | a0019 | c0058 | t0001 | g0163 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02818 | hp2 | a0001 | c0037 | t0001 | g0127 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02895 | hp2 | a0006 | c0007 | t0003 | g0162 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0334 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02896 | hp2 | a0003 | c0019 | t0003 | g0137 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0333 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02897 | hp2 | a0006 | c0007 | t0003 | g0161 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02965 | hp1 | a0005 | c0049 | t0004 | g0171 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0076 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0104 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02970 | hp2 | a0010 | c0016 | t0001 | g0056 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02976 | hp1 | a0003 | c0005 | t0003 | g0135 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02976 | hp2 | a0001 | c0045 | t0002 | g0176 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03017 | hp2 | a0003 | c0005 | t0001 | g0147 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03041 | hp1 | a0007 | c0013 | t0001 | g0192 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03098 | hp1 | a0020 | c0036 | t0003 | g0132 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03130 | hp1 | a0001 | c0004 | t0003 | g0115 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03130 | hp2 | a0010 | c0015 | t0003 | g0053 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03139 | hp1 | a0006 | c0007 | t0003 | g0164 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0090 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03209 | hp1 | a0011 | c0012 | t0003 | g0051 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03209 | hp2 | a0006 | c0007 | t0003 | g0160 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03225 | hp1 | a0005 | c0009 | t0004 | g0166 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03225 | hp2 | a0021 | c0047 | t0002 | g0287 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03453 | hp2 | a0001 | c0004 | t0003 | g0078 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03486 | hp2 | a0001 | c0004 | t0003 | g0087 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03490 | hp2 | a0001 | c0002 | t0005 | g0001 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03491 | hp2 | a0003 | c0005 | t0001 | g0142 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03492 | hp1 | a0003 | c0005 | t0001 | g0141 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03492 | hp2 | a0001 | c0002 | t0005 | g0002 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0075 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03540 | hp2 | a0022 | c0028 | t0001 | g0057 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03579 | hp1 | a0003 | c0059 | t0001 | g0050 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03704 | hp2 | a0001 | c0050 | t0002 | g0328 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03710 | hp1 | a0002 | c0003 | t0003 | g0031 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0110 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03927 | hp2 | a0003 | c0031 | t0009 | g0140 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03942 | hp2 | a0002 | c0003 | t0003 | g0032 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04204 | hp1 | a0003 | c0018 | t0001 | g0133 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18522 | hp1 | a0006 | c0007 | t0003 | g0199 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18941 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18941 | hp2 | a0023 | c0030 | t0003 | g0198 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18943 | hp2 | a0001 | c0008 | t0001 | g0222 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18945 | hp1 | a0001 | c0004 | t0003 | g0112 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18948 | hp1 | a0013 | c0023 | t0001 | g0048 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18948 | hp2 | a0003 | c0005 | t0001 | g0145 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18949 | hp1 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18950 | hp2 | a0002 | c0003 | t0003 | g0040 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18953 | hp1 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18959 | hp2 | a0024 | c0033 | t0003 | g0018 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18961 | hp1 | a0002 | c0003 | t0003 | g0030 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18961 | hp2 | a0001 | c0004 | t0003 | g0081 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18962 | hp1 | a0001 | c0002 | t0010 | g0186 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18964 | hp2 | a0002 | c0003 | t0003 | g0036 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18970 | hp2 | a0001 | c0010 | t0002 | g0322 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18971 | hp1 | a0001 | c0010 | t0001 | g0125 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18971 | hp2 | a0001 | c0010 | t0004 | g0225 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18973 | hp2 | a0025 | c0024 | t0001 | g0111 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18979 | hp1 | a0001 | c0010 | t0001 | g0126 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18980 | hp1 | a0001 | c0053 | t0002 | g0286 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18983 | hp1 | a0001 | c0004 | t0003 | g0107 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18983 | hp2 | a0001 | c0008 | t0001 | g0216 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18990 | hp1 | a0002 | c0003 | t0003 | g0039 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18990 | hp2 | a0001 | c0004 | t0003 | g0130 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18991 | hp1 | a0013 | c0023 | t0001 | g0060 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA18993 | hp2 | a0001 | c0014 | t0006 | g0215 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19003 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19007 | hp2 | a0003 | c0005 | t0001 | g0144 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19010 | hp1 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19043 | hp1 | a0026 | c0027 | t0003 | g0134 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19043 | hp2 | a0003 | c0005 | t0003 | g0063 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19055 | hp2 | a0002 | c0003 | t0003 | g0019 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19056 | hp1 | a0002 | c0003 | t0003 | g0025 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19056 | hp2 | a0001 | c0008 | t0001 | g0221 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19057 | hp2 | a0003 | c0005 | t0001 | g0156 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19063 | hp1 | a0027 | c0041 | t0001 | g0062 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19063 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19064 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19064 | hp2 | a0001 | c0004 | t0003 | g0014 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19065 | hp2 | a0003 | c0005 | t0001 | g0157 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19066 | hp2 | a0003 | c0005 | t0001 | g0143 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19067 | hp1 | a0003 | c0018 | t0001 | g0152 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19074 | hp1 | a0028 | c0029 | t0003 | g0188 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19074 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19079 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19081 | hp2 | a0029 | c0051 | t0004 | g0291 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19085 | hp2 | a0002 | c0003 | t0003 | g0033 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19086 | hp1 | a0030 | c0034 | t0003 | g0010 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19086 | hp2 | a0003 | c0005 | t0003 | g0154 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19087 | hp1 | a0008 | c0040 | t0003 | g0187 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19087 | hp2 | a0031 | c0035 | t0003 | g0012 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19088 | hp1 | a0001 | c0008 | t0001 | g0211 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19088 | hp2 | a0001 | c0004 | t0003 | g0114 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19091 | hp1 | a0001 | c0008 | t0001 | g0203 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19240 | hp1 | a0011 | c0012 | t0003 | g0201 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20129 | hp1 | a0010 | c0016 | t0001 | g0054 | AFR | ASW | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0117 | AFR | ASW | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | TSI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20752 | hp2 | a0002 | c0003 | t0003 | g0035 | EUR | TSI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0092 | SAS | GIH | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | GIH | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01123 | hp1 | a0004 | c0025 | t0002 | g0247 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG01123 | hp2 | a0001 | c0004 | t0001 | g0065 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02486 | hp1 | a0005 | c0009 | t0004 | g0183 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02486 | hp2 | a0010 | c0015 | t0003 | g0055 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03471 | hp1 | a0003 | c0019 | t0003 | g0136 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG03471 | hp2 | a0001 | c0004 | t0003 | g0189 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG06807 | hp1 | a0011 | c0012 | t0003 | g0052 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
HG06807 | hp2 | a0006 | c0007 | t0003 | g0159 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
NA21309 | hp2 | a0011 | c0012 | t0003 | g0202 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0284 | REF | REF | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0292 | REF | REF | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1511024 | C | T | 1 | a0029 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.4309G>A | p.Glu1437Lys | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 4635/5232 | 4309/4389 | 1437/1462 | chr16 | 1511024 | |||
chr16:1511069 | C | T | 1 | a0026 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4264G>A | p.Ala1422Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 4590/5232 | 4264/4389 | 1422/1462 | chr16 | 1511069 | |||
chr16:1519933 | C | T | 1 | a0014 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.3988G>A | p.Ala1330Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/31 | 4314/5232 | 3988/4389 | 1330/1462 | chr16 | 1519933 | |||
chr16:1520261 | A | G | 1 | a0005 | 8 | HG01070.hp1 HG01884.hp1 HG02165.hp2 others(5): Show |
missense_variant | MODERATE | c.3743T>C | p.Ile1248Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/31 | 4069/5232 | 3743/4389 | 1248/1462 | chr16 | 1520261 | |||
chr16:1520660 | C | T | 1 | a0030 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.3602G>A | p.Arg1201His | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/31 | 3928/5232 | 3602/4389 | 1201/1462 | chr16 | 1520660 | |||
chr16:1523889 | G | A | 6 | a0002 a0008 a0023 others(3): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
missense_variant | MODERATE | c.3209C>T | p.Ala1070Val | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/31 | 3535/5232 | 3209/4389 | 1070/1462 | chr16 | 1523889 | |||
chr16:1524614 | C | T | 1 | a0027 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.3079G>A | p.Gly1027Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/31 | 3405/5232 | 3079/4389 | 1027/1462 | chr16 | 1524614 | |||
chr16:1525900 | G | C | 1 | a0031 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.2755C>G | p.Arg919Gly | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/31 | 3081/5232 | 2755/4389 | 919/1462 | chr16 | 1525900 | |||
chr16:1525909 | C | T | 1 | a0021 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.2746G>A | p.Asp916Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/31 | 3072/5232 | 2746/4389 | 916/1462 | chr16 | 1525909 | |||
chr16:1557974 | T | C | 1 | a0012 | 2 | HG00642.hp1 HG01099.hp2 |
missense_variant | MODERATE | c.2360A>G | p.Asp787Gly | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2686/5232 | 2360/4389 | 787/1462 | chr16 | 1557974 | |||
chr16:1558004 | A | C | 1 | a0010 | 4 | HG02486.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
missense_variant | MODERATE | c.2330T>G | p.Leu777Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2656/5232 | 2330/4389 | 777/1462 | chr16 | 1558004 | |||
chr16:1558016 | C | T | 1 | a0016 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2318G>A | p.Arg773Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2644/5232 | 2318/4389 | 773/1462 | chr16 | 1558016 | |||
chr16:1562046 | C | T | 1 | a0028 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.2138G>A | p.Arg713Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/31 | 2464/5232 | 2138/4389 | 713/1462 | chr16 | 1562046 | |||
chr16:1564007 | G | C | 1 | a0020 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2057C>G | p.Ala686Gly | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2383/5232 | 2057/4389 | 686/1462 | chr16 | 1564007 | |||
chr16:1564056 | G | A | 1 | a0007 | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
missense_variant | MODERATE | c.2008C>T | p.Pro670Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2334/5232 | 2008/4389 | 670/1462 | chr16 | 1564056 | |||
chr16:1564146 | C | T | 2 | a0007 a0020 |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
missense_variant | MODERATE | c.1918G>A | p.Asp640Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2244/5232 | 1918/4389 | 640/1462 | chr16 | 1564146 | |||
chr16:1566200 | C | T | 5 | a0002 a0009 a0024 others(2): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
missense_variant | MODERATE | c.1862G>A | p.Arg621Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/31 | 2188/5232 | 1862/4389 | 621/1462 | chr16 | 1566200 | |||
chr16:1566231 | C | T | 2 | a0022 a0026 |
2 | HG03540.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1831G>A | p.Val611Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/31 | 2157/5232 | 1831/4389 | 611/1462 | chr16 | 1566231 | |||
chr16:1568305 | C | T | 2 | a0006 a0011 |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
missense_variant | MODERATE | c.1682G>A | p.Ser561Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/31 | 2008/5232 | 1682/4389 | 561/1462 | chr16 | 1568305 | |||
chr16:1568320 | T | C | 1 | a0017 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1667A>G | p.His556Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/31 | 1993/5232 | 1667/4389 | 556/1462 | chr16 | 1568320 | |||
chr16:1583341 | G | T | 1 | a0024 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.1405C>A | p.Leu469Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/31 | 1731/5232 | 1405/4389 | 469/1462 | chr16 | 1583341 | |||
chr16:1584224 | G | A | 2 | a0006 a0011 |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
missense_variant | MODERATE | c.1352C>T | p.Ala451Val | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1678/5232 | 1352/4389 | 451/1462 | chr16 | 1584224 | |||
chr16:1584240 | T | C | 1 | a0015 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1336A>G | p.Ile446Val | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1662/5232 | 1336/4389 | 446/1462 | chr16 | 1584240 | |||
chr16:1584384 | C | T | 6 | a0003 a0010 a0022 others(3): Show |
35 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(32): Show |
missense_variant | MODERATE | c.1192G>A | p.Val398Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1518/5232 | 1192/4389 | 398/1462 | chr16 | 1584384 | |||
chr16:1587996 | C | T | 1 | a0007 | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
missense_variant | MODERATE | c.839G>A | p.Arg280Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1165/5232 | 839/4389 | 280/1462 | chr16 | 1587996 | |||
chr16:1587997 | G | A | 2 | a0006 a0019 |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.838C>T | p.Arg280Trp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1164/5232 | 838/4389 | 280/1462 | chr16 | 1587997 | |||
chr16:1587999 | C | G | 1 | a0004 | 9 | HG00733.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
missense_variant | MODERATE | c.836G>C | p.Arg279Pro | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1162/5232 | 836/4389 | 279/1462 | chr16 | 1587999 | |||
chr16:1589643 | T | A | 1 | a0013 | 2 | NA18948.hp1 NA18991.hp1 |
missense_variant | MODERATE | c.772A>T | p.Thr258Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/31 | 1098/5232 | 772/4389 | 258/1462 | chr16 | 1589643 | |||
chr16:1592284 | C | T | 1 | a0025 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.526G>A | p.Gly176Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/31 | 852/5232 | 526/4389 | 176/1462 | chr16 | 1592284 | |||
chr16:1592500 | G | A | 1 | a0018 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.458C>T | p.Thr153Met | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/31 | 784/5232 | 458/4389 | 153/1462 | chr16 | 1592500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1510953 | G | A | 4 | a0003c0017 a0003c0059 a0010c0016 others(1): Show |
6 | HG01243.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.4380C>T | p.Asp1460Asp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 4706/5232 | 4380/4389 | 1460/1462 | chr16 | 1510953 | |||
chr16:1518234 | C | T | 1 | a0001c0050 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4164G>A | p.Arg1388Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/31 | 4490/5232 | 4164/4389 | 1388/1462 | chr16 | 1518234 | |||
chr16:1519931 | C | T | 2 | a0003c0031 a0005c0049 |
2 | HG02965.hp1 HG03927.hp2 |
synonymous_variant | LOW | c.3990G>A | p.Ala1330Ala | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/31 | 4316/5232 | 3990/4389 | 1330/1462 | chr16 | 1519931 | |||
chr16:1520194 | G | A | 1 | a0001c0043 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.3810C>T | p.Ile1270Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/31 | 4136/5232 | 3810/4389 | 1270/1462 | chr16 | 1520194 | |||
chr16:1523951 | G | A | 1 | a0001c0052 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.3147C>T | p.Asn1049Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/31 | 3473/5232 | 3147/4389 | 1049/1462 | chr16 | 1523951 | |||
chr16:1524859 | C | T | 1 | a0001c0048 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.2922G>A | p.Ala974Ala | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/31 | 3248/5232 | 2922/4389 | 974/1462 | chr16 | 1524859 | |||
chr16:1524862 | G | A | 17 | a0001c0002 a0001c0008 a0001c0010 others(14): Show |
92 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
synonymous_variant | LOW | c.2919C>T | p.Ala973Ala | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/31 | 3245/5232 | 2919/4389 | 973/1462 | chr16 | 1524862 | |||
chr16:1526036 | G | A | 1 | a0001c0053 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.2619C>T | p.Asp873Asp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/31 | 2945/5232 | 2619/4389 | 873/1462 | chr16 | 1526036 | |||
chr16:1526742 | G | A | 3 | a0003c0031 a0003c0032 a0007c0013 |
6 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.2454C>T | p.Asp818Asp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/31 | 2780/5232 | 2454/4389 | 818/1462 | chr16 | 1526742 | |||
chr16:1558039 | C | T | 1 | a0001c0037 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.2295G>A | p.Leu765Leu | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2621/5232 | 2295/4389 | 765/1462 | chr16 | 1558039 | |||
chr16:1558081 | A | G | 23 | a0001c0002 a0001c0004 a0001c0008 others(20): Show |
124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
synonymous_variant | LOW | c.2253T>C | p.Pro751Pro | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2579/5232 | 2253/4389 | 751/1462 | chr16 | 1558081 | |||
chr16:1558087 | G | A | 3 | a0001c0020 a0003c0019 a0020c0036 |
5 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.2247C>T | p.His749His | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2573/5232 | 2247/4389 | 749/1462 | chr16 | 1558087 | |||
chr16:1564096 | A | G | 45 | a0001c0002 a0001c0004 a0001c0008 others(42): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
synonymous_variant | LOW | c.1968T>C | p.Ser656Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2294/5232 | 1968/4389 | 656/1462 | chr16 | 1564096 | |||
chr16:1566238 | T | C | 1 | a0001c0054 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.1824A>G | p.Thr608Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/31 | 2150/5232 | 1824/4389 | 608/1462 | chr16 | 1566238 | |||
chr16:1584346 | C | T | 1 | a0001c0008 | 5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
synonymous_variant | LOW | c.1230G>A | p.Ser410Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1556/5232 | 1230/4389 | 410/1462 | chr16 | 1584346 | |||
chr16:1586202 | G | A | 2 | a0001c0014 a0001c0057 |
4 | HG02080.hp1 HG02080.hp2 HG02523.hp2 others(1): Show |
synonymous_variant | LOW | c.1083C>T | p.Pro361Pro | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/31 | 1409/5232 | 1083/4389 | 361/1462 | chr16 | 1586202 | |||
chr16:1588007 | T | C | 1 | a0003c0059 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.828A>G | p.Lys276Lys | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1154/5232 | 828/4389 | 276/1462 | chr16 | 1588007 | |||
chr16:1592499 | C | A | 2 | a0007c0013 a0007c0060 |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
synonymous_variant | LOW | c.459G>T | p.Thr153Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/31 | 785/5232 | 459/4389 | 153/1462 | chr16 | 1592499 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1510541 | C | T | 1 | a0001c0014t0006 | 2 | HG02523.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 403 | chr16 | 1510541 | ||||||
chr16:1510709 | G | T | 1 | a0001c0014t0006 | 2 | HG02523.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*235C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 235 | chr16 | 1510709 | ||||||
chr16:1510881 | T | C | 1 | a0001c0001t0007 | 2 | HG00323.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*63A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 63 | chr16 | 1510881 | ||||||
chr16:1510885 | A | G | 38 | a0001c0001t0004 a0001c0002t0001 a0001c0002t0005 others(35): Show |
137 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*59T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 59 | chr16 | 1510885 | ||||||
chr16:1510932 | G | A | 1 | a0003c0031t0009 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 12 | chr16 | 1510932 | ||||||
chr16:1510942 | C | T | 1 | a0001c0002t0005 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 2 | chr16 | 1510942 | ||||||
chr16:1607283 | C | G | 50 | a0001c0001t0003 a0001c0002t0001 a0001c0002t0003 others(47): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
5_prime_UTR_variant | MODIFIER | c.-17G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/31 | 17 | chr16 | 1607283 | ||||||
chr16:1610755 | G | A | 1 | a0001c0002t0010 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/31 | 3489 | chr16 | 1610755 | ||||||
chr16:1612013 | C | G | 1 | a0003c0032t0008 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/31 | 4747 | chr16 | 1612013 | ||||||
chr16:1612063 | A | T | 1 | a0001c0002t0005 | 2 | HG03490.hp2 HG03492.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-317T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/31 | chr16 | 1612063 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1511322 | G | A | 32 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(29): Show |
32 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.4183-172C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511322 | |||||||
chr16:1511338 | C | A | 32 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(29): Show |
32 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.4183-188G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511338 | |||||||
chr16:1511416 | C | G | 1 | a0001c0002t0001g0210 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4183-266G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511416 | |||||||
chr16:1511445 | A | G | 158 | a0001c0001t0002g0169 a0001c0001t0002g0180 a0001c0001t0002g0181 others(155): Show |
158 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.4183-295T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511445 | |||||||
chr16:1511487 | G | C | 2 | a0012c0022t0002g0231 a0012c0022t0002g0236 |
2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.4183-337C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511487 | |||||||
chr16:1511581 | G | C | 1 | a0001c0001t0002g0046 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4183-431C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511581 | |||||||
chr16:1511696 | G | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4183-546C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511696 | |||||||
chr16:1511734 | C | CGA | 31 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(28): Show |
31 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4183-586_4183-585d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511734 | |||||||
chr16:1511756 | C | G | 1 | a0001c0001t0002g0259 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4183-606G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511756 | |||||||
chr16:1511827 | CAG | C | 13 | a0001c0002t0001g0113 a0001c0002t0001g0210 a0001c0002t0001g0218 others(10): Show |
13 | HG01433.hp1 HG02071.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.4183-679_4183-678d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511827 | |||||||
chr16:1511964 | A | G | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-814T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511964 | |||||||
chr16:1512025 | T | C | 144 | a0001c0001t0002g0253 a0001c0001t0004g0170 a0001c0001t0004g0172 others(141): Show |
144 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.4183-875A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512025 | |||||||
chr16:1512122 | G | GTGGGGGG others(44): Show |
5 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0003g0135 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4183-1023_4183-973 others(54): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512122 | |||||||
chr16:1512140 | G | A | 2 | a0001c0002t0001g0210 a0001c0043t0001g0219 |
2 | HG02071.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.4183-990C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512140 | |||||||
chr16:1512159 | TGGTGGGG others(34): Show |
T | 7 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.4183-1050_4183-101 others(45): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512159 | |||||||
chr16:1512194 | A | G | 108 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4183-1044T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512194 | |||||||
chr16:1512200 | G | GGGTGAGG others(3): Show |
1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4183-1051_4183-105 others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512200 | |||||||
chr16:1512202 | GTGGGGGG others(5): Show |
G | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4183-1064_4183-105 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512202 | |||||||
chr16:1512251 | C | T | 101 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(98): Show |
101 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.4183-1101G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512251 | |||||||
chr16:1512398 | C | T | 3 | a0001c0002t0001g0061 a0001c0002t0001g0070 a0004c0026t0004g0312 |
3 | HG00280.hp2 HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.4183-1248G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512398 | |||||||
chr16:1512427 | C | T | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.4183-1277G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512427 | |||||||
chr16:1512459 | T | C | 111 | a0001c0001t0002g0252 a0001c0001t0002g0255 a0001c0001t0002g0279 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.4183-1309A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512459 | |||||||
chr16:1512485 | C | G | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4183-1335G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512485 | |||||||
chr16:1512488 | G | C | 5 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(2): Show |
5 | HG02809.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4183-1338C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512488 | |||||||
chr16:1512565 | C | T | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-1415G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512565 | |||||||
chr16:1512625 | C | T | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4183-1475G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512625 | |||||||
chr16:1512721 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4183-1571G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512721 | |||||||
chr16:1512753 | G | A | 30 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(27): Show |
30 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.4183-1603C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512753 | |||||||
chr16:1512803 | G | A | 200 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(197): Show |
200 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.4183-1653C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512803 | |||||||
chr16:1512818 | A | G | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-1668T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512818 | |||||||
chr16:1512821 | C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-1671G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512821 | |||||||
chr16:1512914 | C | G | 36 | a0001c0014t0003g0102 a0002c0003t0003g0006 a0002c0003t0003g0007 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.4183-1764G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512914 | |||||||
chr16:1512934 | G | C | 5 | a0001c0004t0003g0189 a0010c0015t0003g0053 a0010c0015t0003g0055 others(2): Show |
5 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4183-1784C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512934 | |||||||
chr16:1512956 | G | C | 7 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.4183-1806C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512956 | |||||||
chr16:1513073 | C | T | 1 | a0004c0006t0002g0246 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4183-1923G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513073 | |||||||
chr16:1513114 | G | A | 7 | a0001c0004t0001g0074 a0001c0004t0001g0075 a0006c0007t0003g0159 others(4): Show |
7 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4183-1964C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513114 | |||||||
chr16:1513167 | A | G | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4183-2017T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513167 | |||||||
chr16:1513211 | C | G | 1 | a0024c0033t0003g0018 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4183-2061G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513211 | |||||||
chr16:1513215 | C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-2065G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513215 | |||||||
chr16:1513217 | C | T | 1 | a0024c0033t0003g0018 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4183-2067G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513217 | |||||||
chr16:1513227 | C | T | 2 | a0001c0004t0001g0076 a0003c0031t0009g0140 |
2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-2077G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513227 | |||||||
chr16:1513280 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4183-2130C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513280 | |||||||
chr16:1513295 | C | G | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4183-2145G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513295 | |||||||
chr16:1513305 | C | T | 2 | a0001c0001t0002g0263 a0001c0004t0001g0117 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4183-2155G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513305 | |||||||
chr16:1513310 | A | C | 1 | a0001c0001t0002g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4183-2160T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513310 | |||||||
chr16:1513313 | C | T | 2 | a0001c0001t0002g0306 a0001c0001t0002g0309 |
2 | HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.4183-2163G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513313 | |||||||
chr16:1513316 | C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-2166G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513316 | |||||||
chr16:1513418 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4183-2268A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513418 | |||||||
chr16:1513516 | A | G | 2 | a0001c0002t0005g0001 a0001c0002t0005g0002 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4183-2366T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513516 | |||||||
chr16:1513581 | G | A | 97 | a0001c0001t0004g0229 a0001c0002t0001g0005 a0001c0002t0001g0013 others(94): Show |
97 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.4183-2431C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513581 | |||||||
chr16:1513609 | C | A | 1 | a0001c0001t0002g0306 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4183-2459G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513609 | |||||||
chr16:1513632 | T | C | 2 | a0001c0004t0001g0076 a0003c0031t0009g0140 |
2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-2482A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513632 | |||||||
chr16:1513666 | ACTTT | A | 101 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(98): Show |
101 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.4183-2520_4183-251 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513666 | |||||||
chr16:1513671 | C | CT | 38 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.4183-2522dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513671 | |||||||
chr16:1513704 | T | C | 203 | a0001c0001t0002g0004 a0001c0001t0002g0169 a0001c0001t0002g0174 others(200): Show |
203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.4183-2554A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513704 | |||||||
chr16:1513707 | T | C | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4183-2557A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513707 | |||||||
chr16:1513708 | G | C | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4183-2558C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513708 | |||||||
chr16:1513712 | C | G | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4183-2562G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513712 | |||||||
chr16:1513743 | T | G | 7 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.4183-2593A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513743 | |||||||
chr16:1513753 | A | C | 1 | a0002c0003t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.4183-2603T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513753 | |||||||
chr16:1513798 | C | T | 103 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4183-2648G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513798 | |||||||
chr16:1513799 | A | G | 199 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(196): Show |
199 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.4183-2649T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513799 | |||||||
chr16:1513823 | A | G | 8 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.4183-2673T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513823 | |||||||
chr16:1513824 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4183-2674G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513824 | |||||||
chr16:1513831 | A | G | 6 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(3): Show |
6 | HG01891.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4183-2681T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513831 | |||||||
chr16:1513862 | A | C | 4 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-2712T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513862 | |||||||
chr16:1513863 | C | T | 1 | a0002c0003t0003g0034 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4183-2713G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513863 | |||||||
chr16:1513864 | G | A | 152 | a0001c0001t0002g0205 a0001c0001t0002g0235 a0001c0001t0004g0249 others(149): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.4183-2714C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513864 | |||||||
chr16:1513875 | G | A | 3 | a0002c0003t0003g0031 a0011c0012t0003g0201 a0011c0012t0003g0202 |
3 | HG03710.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4183-2725C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513875 | |||||||
chr16:1513875 | G | C | 3 | a0001c0001t0002g0200 a0001c0001t0002g0298 a0020c0036t0003g0132 |
3 | HG02622.hp1 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4183-2725C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513875 | |||||||
chr16:1513885 | A | G | 211 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(208): Show |
211 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.4183-2735T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513885 | |||||||
chr16:1513894 | C | T | 60 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(57): Show |
60 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.4183-2744G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513894 | |||||||
chr16:1513895 | C | G | 209 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(206): Show |
209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.4183-2745G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513895 | |||||||
chr16:1513909 | A | G | 18 | a0001c0001t0002g0324 a0001c0001t0002g0325 a0001c0004t0003g0189 others(15): Show |
18 | HG02056.hp2 HG02074.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.4183-2759T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513909 | |||||||
chr16:1513915 | T | C | 143 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0324 others(140): Show |
143 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.4183-2765A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513915 | |||||||
chr16:1513916 | G | A | 2 | a0001c0001t0002g0324 a0001c0001t0002g0325 |
2 | NA18945.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.4183-2766C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513916 | |||||||
chr16:1513919 | C | T | 127 | a0001c0001t0002g0262 a0001c0001t0002g0280 a0001c0001t0002g0281 others(124): Show |
127 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.4183-2769G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513919 | |||||||
chr16:1513920 | G | A | 13 | a0001c0001t0002g0324 a0001c0001t0002g0325 a0002c0003t0003g0006 others(10): Show |
13 | HG02056.hp2 HG02074.hp2 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.4183-2770C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513920 | |||||||
chr16:1513924 | T | C | 11 | a0002c0003t0003g0006 a0002c0003t0003g0023 a0002c0003t0003g0025 others(8): Show |
11 | HG02056.hp2 HG02074.hp2 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.4183-2774A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513924 | |||||||
chr16:1513958 | C | T | 6 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(3): Show |
6 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4183-2808G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513958 | |||||||
chr16:1513962 | T | C | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-2812A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513962 | |||||||
chr16:1513965 | A | G | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-2815T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513965 | |||||||
chr16:1513968 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4183-2818G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513968 | |||||||
chr16:1514135 | A | G | 4 | a0002c0003t0003g0020 a0002c0003t0003g0026 a0024c0033t0003g0018 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-2985T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514135 | |||||||
chr16:1514143 | T | C | 4 | a0002c0003t0003g0020 a0002c0003t0003g0026 a0024c0033t0003g0018 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-2993A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514143 | |||||||
chr16:1514151 | G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4183-3001C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514151 | |||||||
chr16:1514164 | C | G | 9 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.4183-3014G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514164 | |||||||
chr16:1514164 | C | T | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4183-3014G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514164 | |||||||
chr16:1514165 | G | A | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4183-3015C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514165 | |||||||
chr16:1514185 | G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-3035C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514185 | |||||||
chr16:1514238 | C | T | 2 | a0001c0001t0002g0174 a0002c0003t0003g0007 |
2 | NA18941.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4183-3088G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514238 | |||||||
chr16:1514301 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4183-3151G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514301 | |||||||
chr16:1514349 | G | A | 53 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(50): Show |
53 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.4183-3199C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514349 | |||||||
chr16:1514351 | T | C | 2 | a0001c0004t0001g0076 a0003c0031t0009g0140 |
2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-3201A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514351 | |||||||
chr16:1514356 | C | T | 2 | a0001c0004t0001g0076 a0003c0031t0009g0140 |
2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-3206G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514356 | |||||||
chr16:1514369 | C | CAAATAAA others(5): Show |
1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-3231_4183-322 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514369 | |||||||
chr16:1514369 | C | CAAATAAA others(13): Show |
1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4183-3239_4183-322 others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514369 | |||||||
chr16:1514369 | CAAATAAA others(5): Show |
C | 1 | a0001c0001t0002g0289 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4183-3231_4183-322 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514369 | |||||||
chr16:1514533 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4183-3383C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514533 | |||||||
chr16:1514692 | T | C | 1 | a0001c0001t0004g0272 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4182+3524A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514692 | |||||||
chr16:1514750 | A | G | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4182+3466T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514750 | |||||||
chr16:1514822 | G | A | 96 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(93): Show |
96 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.4182+3394C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514822 | |||||||
chr16:1515115 | C | A | 37 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.4182+3101G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515115 | |||||||
chr16:1515407 | C | G | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4182+2809G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515407 | |||||||
chr16:1515425 | G | T | 2 | a0001c0004t0001g0076 a0003c0031t0009g0140 |
2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4182+2791C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515425 | |||||||
chr16:1515539 | C | T | 196 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(193): Show |
196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.4182+2677G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515539 | |||||||
chr16:1515844 | C | T | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4182+2372G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515844 | |||||||
chr16:1515892 | A | T | 35 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(32): Show |
35 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.4182+2324T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515892 | |||||||
chr16:1516019 | A | C | 1 | a0001c0001t0002g0257 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4182+2197T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516019 | |||||||
chr16:1516033 | C | T | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4182+2183G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516033 | |||||||
chr16:1516036 | A | G | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4182+2180T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516036 | |||||||
chr16:1516139 | C | CA | 7 | a0001c0001t0002g0206 a0001c0001t0002g0255 a0001c0001t0002g0266 others(4): Show |
7 | HG00673.hp2 HG01516.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.4182+2076dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | C | CAA | 41 | a0001c0001t0002g0233 a0001c0001t0002g0239 a0001c0001t0002g0250 others(38): Show |
41 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.4182+2075_4182+207 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | C | CAAA | 38 | a0001c0001t0002g0004 a0001c0001t0002g0046 a0001c0001t0002g0179 others(35): Show |
38 | HG00544.hp2 HG01081.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.4182+2074_4182+207 others(7): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | C | CAAAA | 24 | a0001c0001t0002g0178 a0001c0001t0002g0205 a0001c0001t0002g0234 others(21): Show |
24 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.4182+2073_4182+207 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0304 a0001c0001t0002g0307 |
2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4182+2066_4182+207 others(15): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | CAAAAAAA others(5): Show |
C | 16 | a0001c0001t0002g0227 a0001c0001t0002g0232 a0001c0002t0001g0013 others(13): Show |
16 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.4182+2065_4182+207 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | CAAAAAAA others(6): Show |
C | 103 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0004g0226 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4182+2064_4182+207 others(17): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | CAAAAAAA others(7): Show |
C | 78 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.4182+2063_4182+207 others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | CAAAAAAA others(8): Show |
C | 3 | a0002c0003t0003g0006 a0002c0003t0003g0029 a0003c0005t0001g0142 |
3 | HG03491.hp2 NA19003.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.4182+2062_4182+207 others(19): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516139 | CAAAAAAA others(16): Show |
C | 3 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0004t0003g0081 |
3 | HG00423.hp2 NA18961.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.4182+2054_4182+207 others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | |||||||
chr16:1516169 | A | C | 1 | a0001c0004t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4182+2047T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516169 | |||||||
chr16:1516174 | A | C | 1 | a0003c0005t0001g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4182+2042T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516174 | |||||||
chr16:1516176 | A | C | 198 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(195): Show |
198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.4182+2040T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516176 | |||||||
chr16:1516177 | A | C | 198 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(195): Show |
198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.4182+2039T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516177 | |||||||
chr16:1516198 | A | G | 4 | a0001c0004t0003g0189 a0010c0015t0003g0053 a0011c0012t0003g0051 others(1): Show |
4 | HG03130.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4182+2018T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516198 | |||||||
chr16:1516283 | T | C | 195 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(192): Show |
195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.4182+1933A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516283 | |||||||
chr16:1516381 | A | G | 55 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(52): Show |
55 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.4182+1835T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516381 | |||||||
chr16:1516498 | G | GGTGGCTC others(126): Show |
1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4182+1717_4182+171 others(137): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516498 | |||||||
chr16:1516540 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4182+1676G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516540 | |||||||
chr16:1516541 | G | A | 2 | a0001c0001t0002g0252 a0001c0001t0002g0255 |
2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4182+1675C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516541 | |||||||
chr16:1516568 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4182+1648C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516568 | |||||||
chr16:1516585 | C | T | 104 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.4182+1631G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516585 | |||||||
chr16:1516596 | T | C | 199 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(196): Show |
199 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.4182+1620A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516596 | |||||||
chr16:1516631 | G | A | 5 | a0001c0001t0004g0226 a0001c0002t0001g0013 a0003c0005t0001g0141 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.4182+1585C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516631 | |||||||
chr16:1516638 | C | T | 4 | a0001c0001t0004g0226 a0003c0005t0001g0141 a0003c0005t0001g0142 others(1): Show |
4 | HG02145.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.4182+1578G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516638 | |||||||
chr16:1516680 | G | A | 1 | a0030c0034t0003g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4182+1536C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516680 | |||||||
chr16:1516722 | A | G | 33 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(30): Show |
33 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.4182+1494T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516722 | |||||||
chr16:1516769 | C | CA | 22 | a0001c0001t0002g0180 a0001c0001t0002g0230 a0001c0001t0002g0237 others(19): Show |
22 | HG01192.hp2 HG01361.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.4182+1446dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516769 | |||||||
chr16:1516769 | CA | C | 23 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(20): Show |
23 | HG00621.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.4182+1446delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516769 | |||||||
chr16:1516825 | G | A | 105 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(102): Show |
105 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4182+1391C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516825 | |||||||
chr16:1517049 | A | G | 1 | a0001c0001t0002g0293 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4182+1167T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517049 | |||||||
chr16:1517089 | G | A | 1 | a0007c0060t0001g0195 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4182+1127C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517089 | |||||||
chr16:1517109 | G | T | 3 | a0006c0007t0003g0159 a0006c0007t0003g0161 a0006c0007t0003g0162 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4182+1107C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517109 | |||||||
chr16:1517366 | AAG | A | 93 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(90): Show |
93 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.4182+848_4182+849d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517366 | |||||||
chr16:1517367 | AG | A | 99 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(96): Show |
99 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.4182+848delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517367 | |||||||
chr16:1517368 | G | A | 5 | a0001c0002t0001g0049 a0001c0002t0001g0224 a0003c0018t0001g0152 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.4182+848C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517368 | |||||||
chr16:1517452 | GAGA | G | 80 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(77): Show |
80 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.4182+761_4182+763d others(5): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517452 | |||||||
chr16:1517589 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4182+627C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517589 | |||||||
chr16:1517650 | A | G | 196 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(193): Show |
196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.4182+566T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517650 | |||||||
chr16:1517693 | G | A | 196 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(193): Show |
196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.4182+523C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517693 | |||||||
chr16:1517772 | C | T | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4182+444G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517772 | |||||||
chr16:1517787 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4182+429G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517787 | |||||||
chr16:1517869 | G | A | 2 | a0001c0004t0001g0074 a0001c0004t0001g0075 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4182+347C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517869 | |||||||
chr16:1517973 | G | C | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4182+243C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517973 | |||||||
chr16:1517987 | G | C | 11 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.4182+229C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517987 | |||||||
chr16:1518150 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4182+66C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1518150 | |||||||
chr16:1518401 | A | G | 106 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4041-44T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518401 | |||||||
chr16:1518448 | G | T | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4041-91C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518448 | |||||||
chr16:1518534 | G | T | 1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4041-177C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518534 | |||||||
chr16:1518578 | A | G | 2 | a0001c0001t0002g0282 a0001c0001t0002g0285 |
2 | HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.4041-221T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518578 | |||||||
chr16:1518692 | G | C | 7 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0009 others(4): Show |
7 | HG00408.hp1 HG00544.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.4041-335C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518692 | |||||||
chr16:1518706 | G | A | 1 | a0003c0018t0001g0152 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4041-349C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518706 | |||||||
chr16:1518790 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4041-433G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518790 | |||||||
chr16:1519002 | A | T | 6 | a0001c0002t0001g0212 a0001c0002t0001g0213 a0001c0002t0001g0217 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.4041-645T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519002 | |||||||
chr16:1519137 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4040+744G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519137 | |||||||
chr16:1519160 | G | A | 4 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.4040+721C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519160 | |||||||
chr16:1519185 | G | A | 2 | a0001c0001t0002g0304 a0001c0001t0002g0307 |
2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4040+696C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519185 | |||||||
chr16:1519201 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.4040+680G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519201 | |||||||
chr16:1519217 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4040+664T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519217 | |||||||
chr16:1519251 | G | A | 106 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4040+630C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519251 | |||||||
chr16:1519300 | G | A | 37 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.4040+581C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519300 | |||||||
chr16:1519307 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.4040+574G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519307 | |||||||
chr16:1519351 | G | A | 1 | a0004c0006t0002g0241 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4040+530C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519351 | |||||||
chr16:1519404 | T | C | 61 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(58): Show |
61 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.4040+477A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519404 | |||||||
chr16:1519523 | A | C | 202 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(199): Show |
202 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.4040+358T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519523 | |||||||
chr16:1519566 | C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4040+315G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519566 | |||||||
chr16:1519710 | G | A | 30 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(27): Show |
30 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.4040+171C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519710 | |||||||
chr16:1519828 | G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4040+53C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519828 | |||||||
chr16:1519830 | C | G | 1 | a0018c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4040+51G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519830 | |||||||
chr16:1519871 | G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4040+10C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519871 | |||||||
chr16:1519875 | G | A | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | splice_region_variant&intron_variant | LOW | c.4040+6C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519875 | |||||||
chr16:1520058 | G | A | 2 | a0012c0022t0002g0231 a0012c0022t0002g0236 |
2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.3874-11C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520058 | |||||||
chr16:1520075 | G | T | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3874-28C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520075 | |||||||
chr16:1520096 | C | T | 1 | a0010c0016t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3873+35G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520096 | |||||||
chr16:1520107 | T | C | 1 | a0010c0016t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3873+24A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520107 | |||||||
chr16:1520387 | C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3661-44G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/30 | chr16 | 1520387 | |||||||
chr16:1520448 | C | T | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3661-105G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/30 | chr16 | 1520448 | |||||||
chr16:1520537 | G | A | 2 | a0001c0001t0002g0169 a0001c0001t0002g0184 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3660+65C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/30 | chr16 | 1520537 | |||||||
chr16:1520856 | T | C | 208 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(205): Show |
208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.3454-48A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1520856 | |||||||
chr16:1521119 | T | G | 112 | a0001c0001t0002g0230 a0001c0001t0002g0248 a0001c0001t0002g0299 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.3454-311A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521119 | |||||||
chr16:1521273 | C | T | 1 | a0006c0007t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3454-465G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521273 | |||||||
chr16:1521328 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3454-520T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521328 | |||||||
chr16:1521355 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3454-547G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521355 | |||||||
chr16:1521360 | C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3454-552G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521360 | |||||||
chr16:1521810 | T | C | 201 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(198): Show |
201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3454-1002A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521810 | |||||||
chr16:1521861 | G | GA | 42 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0181 others(39): Show |
42 | HG01192.hp1 HG01243.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.3454-1054dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521861 | |||||||
chr16:1521868 | A | C | 9 | a0001c0001t0002g0180 a0001c0002t0001g0098 a0006c0007t0003g0159 others(6): Show |
9 | HG02109.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3454-1060T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521868 | |||||||
chr16:1521917 | T | A | 6 | a0001c0001t0002g0253 a0001c0002t0001g0129 a0001c0020t0003g0138 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3454-1109A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521917 | |||||||
chr16:1521917 | TA | T | 62 | a0001c0001t0002g0169 a0001c0001t0002g0181 a0001c0001t0002g0182 others(59): Show |
62 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.3454-1110delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521917 | |||||||
chr16:1521917 | TAAA | T | 6 | a0001c0004t0003g0189 a0003c0005t0003g0063 a0010c0015t0003g0053 others(3): Show |
6 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3454-1112_3454-111 others(7): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521917 | |||||||
chr16:1521953 | T | G | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3454-1145A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521953 | |||||||
chr16:1521954 | G | T | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3454-1146C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521954 | |||||||
chr16:1522040 | T | G | 1 | a0001c0002t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3454-1232A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522040 | |||||||
chr16:1522139 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3454-1331T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522139 | |||||||
chr16:1522218 | G | T | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3453+1300C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522218 | |||||||
chr16:1522281 | C | T | 103 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.3453+1237G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522281 | |||||||
chr16:1522313 | T | C | 201 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(198): Show |
201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3453+1205A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522313 | |||||||
chr16:1522348 | C | G | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3453+1170G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522348 | |||||||
chr16:1522362 | A | T | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3453+1156T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522362 | |||||||
chr16:1522392 | G | A | 104 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.3453+1126C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522392 | |||||||
chr16:1522568 | T | C | 201 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(198): Show |
201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3453+950A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522568 | |||||||
chr16:1522593 | C | T | 37 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.3453+925G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522593 | |||||||
chr16:1522764 | G | A | 4 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3453+754C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522764 | |||||||
chr16:1522773 | G | C | 4 | a0001c0001t0002g0290 a0001c0001t0002g0294 a0001c0001t0002g0296 others(1): Show |
4 | NA18962.hp2 NA18991.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3453+745C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522773 | |||||||
chr16:1522850 | G | A | 5 | a0001c0004t0003g0189 a0010c0015t0003g0053 a0010c0015t0003g0055 others(2): Show |
5 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3453+668C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522850 | |||||||
chr16:1523159 | C | T | 1 | a0001c0002t0001g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3453+359G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523159 | |||||||
chr16:1523168 | A | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3453+350T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523168 | |||||||
chr16:1523218 | C | CA | 10 | a0001c0001t0002g0205 a0001c0001t0002g0269 a0001c0001t0002g0323 others(7): Show |
10 | HG01109.hp2 HG01192.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.3453+299dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523218 | |||||||
chr16:1523218 | CA | C | 105 | a0001c0001t0003g0038 a0001c0001t0007g0265 a0001c0001t0007g0270 others(102): Show |
105 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.3453+299delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523218 | |||||||
chr16:1523234 | A | G | 4 | a0001c0004t0003g0189 a0010c0015t0003g0053 a0010c0015t0003g0055 others(1): Show |
4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3453+284T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523234 | |||||||
chr16:1523245 | G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3453+273C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523245 | |||||||
chr16:1523283 | T | G | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3453+235A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523283 | |||||||
chr16:1523484 | G | A | 79 | a0001c0001t0002g0169 a0001c0001t0002g0180 a0001c0001t0002g0181 others(76): Show |
79 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.3453+34C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523484 | |||||||
chr16:1523738 | C | T | 1 | a0001c0001t0002g0323 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3271-38G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/30 | chr16 | 1523738 | |||||||
chr16:1523753 | C | T | 68 | a0001c0001t0002g0282 a0001c0001t0002g0285 a0001c0002t0001g0005 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.3271-53G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/30 | chr16 | 1523753 | |||||||
chr16:1523796 | C | T | 1 | a0001c0001t0002g0323 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3270+32G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/30 | chr16 | 1523796 | |||||||
chr16:1524029 | G | C | 22 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0205 others(19): Show |
22 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.3142-73C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524029 | |||||||
chr16:1524032 | C | T | 4 | a0009c0011t0003g0042 a0009c0011t0003g0043 a0009c0011t0003g0044 others(1): Show |
4 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3142-76G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524032 | |||||||
chr16:1524033 | G | A | 1 | a0018c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3142-77C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524033 | |||||||
chr16:1524169 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3142-213T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524169 | |||||||
chr16:1524251 | A | G | 254 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(251): Show |
254 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.3142-295T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524251 | |||||||
chr16:1524407 | G | A | 2 | a0001c0001t0002g0301 a0001c0045t0002g0176 |
2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3141+145C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524407 | |||||||
chr16:1524422 | T | C | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3141+130A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524422 | |||||||
chr16:1524448 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3141+104C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524448 | |||||||
chr16:1524761 | C | T | 1 | a0005c0009t0004g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2997+23G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/30 | chr16 | 1524761 | |||||||
chr16:1524772 | C | T | 1 | a0001c0001t0002g0320 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2997+12G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/30 | chr16 | 1524772 | |||||||
chr16:1524773 | G | A | 1 | a0001c0014t0003g0102 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2997+11C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/30 | chr16 | 1524773 | |||||||
chr16:1524967 | C | T | 14 | a0001c0001t0004g0226 a0001c0001t0004g0272 a0001c0004t0001g0084 others(11): Show |
14 | HG01192.hp1 HG02015.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2865-51G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1524967 | |||||||
chr16:1525154 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2864+77G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1525154 | |||||||
chr16:1525200 | C | T | 2 | a0001c0020t0003g0138 a0001c0020t0003g0139 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2864+31G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1525200 | |||||||
chr16:1525201 | G | A | 4 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(1): Show |
4 | HG02109.hp1 HG02886.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2864+30C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1525201 | |||||||
chr16:1525434 | G | A | 1 | a0005c0044t0004g0168 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2769-108C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525434 | |||||||
chr16:1525445 | TC | T | 4 | a0010c0015t0003g0053 a0010c0015t0003g0055 a0011c0012t0003g0051 others(1): Show |
4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-120delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525445 | |||||||
chr16:1525449 | G | GCA | 4 | a0010c0015t0003g0053 a0010c0015t0003g0055 a0011c0012t0003g0051 others(1): Show |
4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-124_2769-123i others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525449 | |||||||
chr16:1525450 | G | C | 4 | a0010c0015t0003g0053 a0010c0015t0003g0055 a0011c0012t0003g0051 others(1): Show |
4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-124C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525450 | |||||||
chr16:1525547 | C | T | 6 | a0001c0001t0002g0240 a0001c0001t0002g0318 a0001c0001t0002g0319 others(3): Show |
6 | HG03491.hp1 NA18945.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.2769-221G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525547 | |||||||
chr16:1525581 | G | C | 4 | a0001c0001t0002g0174 a0001c0004t0001g0076 a0003c0031t0009g0140 others(1): Show |
4 | HG02965.hp2 HG03098.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2769-255C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525581 | |||||||
chr16:1525601 | C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2769-275G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525601 | |||||||
chr16:1525636 | G | C | 1 | a0001c0050t0002g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2768+251C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525636 | |||||||
chr16:1525649 | C | T | 2 | a0001c0001t0002g0174 a0001c0004t0001g0076 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2768+238G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525649 | |||||||
chr16:1525684 | G | A | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2768+203C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525684 | |||||||
chr16:1525756 | G | A | 1 | a0007c0013t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2768+131C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525756 | |||||||
chr16:1525838 | C | A | 2 | a0001c0004t0003g0087 a0001c0004t0003g0100 |
2 | HG00639.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2768+49G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525838 | |||||||
chr16:1525859 | G | A | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2768+28C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525859 | |||||||
chr16:1525869 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2768+18G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525869 | |||||||
chr16:1526156 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2578-79G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526156 | |||||||
chr16:1526216 | G | A | 4 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2578-139C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526216 | |||||||
chr16:1526234 | C | T | 6 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2578-157G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526234 | |||||||
chr16:1526235 | G | A | 1 | a0001c0001t0004g0170 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2578-158C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526235 | |||||||
chr16:1526426 | C | G | 31 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(28): Show |
31 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.2577+193G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526426 | |||||||
chr16:1526435 | G | A | 34 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(31): Show |
34 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.2577+184C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526435 | |||||||
chr16:1526610 | G | A | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2577+9C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526610 | |||||||
chr16:1526981 | G | A | 1 | a0001c0001t0002g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2400-185C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1526981 | |||||||
chr16:1527055 | A | G | 217 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0178 others(214): Show |
217 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2400-259T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527055 | |||||||
chr16:1527183 | A | G | 92 | a0001c0001t0002g0174 a0001c0001t0004g0170 a0001c0001t0004g0172 others(89): Show |
92 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2400-387T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527183 | |||||||
chr16:1527229 | C | T | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2400-433G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527229 | |||||||
chr16:1527234 | G | A | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2400-438C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527234 | |||||||
chr16:1527391 | G | C | 1 | a0001c0001t0004g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2400-595C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527391 | |||||||
chr16:1527457 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-661G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527457 | |||||||
chr16:1527534 | G | A | 3 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 |
3 | HG02922.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2400-738C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527534 | |||||||
chr16:1527745 | G | C | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-949C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527745 | |||||||
chr16:1527815 | C | T | 2 | a0007c0013t0001g0191 a0007c0013t0001g0193 |
2 | HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2400-1019G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527815 | |||||||
chr16:1527962 | A | G | 220 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0178 others(217): Show |
220 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.2400-1166T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527962 | |||||||
chr16:1528009 | C | G | 1 | a0001c0002t0001g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2400-1213G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528009 | |||||||
chr16:1528251 | C | G | 34 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(31): Show |
34 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.2400-1455G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528251 | |||||||
chr16:1528294 | C | T | 1 | a0001c0004t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2400-1498G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528294 | |||||||
chr16:1528303 | CCA | C | 24 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(21): Show |
24 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2400-1509_2400-150 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528303 | |||||||
chr16:1528307 | ACACACAC others(21): Show |
A | 8 | a0003c0005t0001g0143 a0003c0005t0001g0144 a0003c0005t0001g0145 others(5): Show |
8 | HG02486.hp2 HG02970.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-1539_2400-151 others(32): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528307 | |||||||
chr16:1528314 | CGCACGCA others(27): Show |
C | 1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2400-1552_2400-151 others(38): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528314 | |||||||
chr16:1528315 | G | GCACGCAT others(19): Show |
1 | a0003c0005t0003g0151 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2400-1545_2400-152 others(30): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528315 | |||||||
chr16:1528315 | GCACGCAT others(19): Show |
G | 37 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(34): Show |
37 | HG00099.hp2 HG00639.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.2400-1545_2400-152 others(30): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528315 | |||||||
chr16:1528318 | CGCATGCA others(49): Show |
C | 1 | a0031c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2400-1578_2400-152 others(60): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528318 | |||||||
chr16:1528328 | CACGTGTG others(23): Show |
C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2400-1562_2400-153 others(34): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528328 | |||||||
chr16:1528334 | T | C | 9 | a0001c0001t0002g0174 a0006c0007t0003g0159 a0006c0007t0003g0160 others(6): Show |
9 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2400-1538A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528334 | |||||||
chr16:1528341 | A | G | 8 | a0003c0005t0001g0143 a0003c0005t0001g0144 a0003c0005t0001g0145 others(5): Show |
8 | HG02486.hp2 HG02970.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-1545T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528341 | |||||||
chr16:1528345 | G | A | 13 | a0001c0001t0002g0174 a0001c0001t0002g0317 a0001c0001t0002g0320 others(10): Show |
13 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.2400-1549C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528345 | |||||||
chr16:1528346 | CATGCACG others(45): Show |
C | 1 | a0001c0014t0006g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2400-1602_2400-155 others(56): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528346 | |||||||
chr16:1528352 | C | G | 3 | a0010c0015t0003g0053 a0010c0015t0003g0055 a0010c0016t0001g0056 |
3 | HG02486.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2400-1556G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528352 | |||||||
chr16:1528360 | T | C | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-1564A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528360 | |||||||
chr16:1528370 | C | T | 4 | a0001c0002t0001g0106 a0001c0004t0003g0112 a0001c0004t0003g0114 others(1): Show |
4 | HG00408.hp2 NA18945.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-1574G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528370 | |||||||
chr16:1528372 | C | G | 7 | a0001c0001t0002g0233 a0003c0031t0009g0140 a0003c0032t0008g0003 others(4): Show |
7 | HG02055.hp2 HG02630.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.2400-1576G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528372 | |||||||
chr16:1528374 | T | C | 2 | a0001c0001t0002g0261 a0001c0050t0002g0328 |
2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2400-1578A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528374 | |||||||
chr16:1528382 | C | T | 6 | a0001c0045t0002g0176 a0005c0009t0004g0166 a0005c0009t0004g0173 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400-1586G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528382 | |||||||
chr16:1528383 | G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2400-1587C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528383 | |||||||
chr16:1528386 | T | C | 1 | a0021c0047t0002g0287 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2400-1590A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528386 | |||||||
chr16:1528398 | G | C | 3 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0005c0009t0004g0167 |
3 | HG01070.hp1 HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2400-1602C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528398 | |||||||
chr16:1528433 | G | GCA | 213 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0178 others(210): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.2400-1639_2400-163 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528433 | |||||||
chr16:1528492 | CACAT | C | 5 | a0001c0004t0001g0104 a0001c0014t0003g0102 a0001c0014t0006g0209 others(2): Show |
5 | HG02080.hp1 HG02523.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400-1700_2400-169 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528492 | |||||||
chr16:1528513 | A | C | 38 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-1717T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528513 | |||||||
chr16:1528543 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-1747C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528543 | |||||||
chr16:1528595 | G | A | 1 | a0001c0001t0002g0297 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2400-1799C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528595 | |||||||
chr16:1528618 | C | T | 1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2400-1822G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528618 | |||||||
chr16:1528724 | G | A | 39 | a0001c0004t0001g0065 a0002c0003t0003g0006 a0002c0003t0003g0007 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2400-1928C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528724 | |||||||
chr16:1528796 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2400-2000C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528796 | |||||||
chr16:1528820 | G | C | 3 | a0011c0012t0003g0051 a0011c0012t0003g0052 a0020c0036t0003g0132 |
3 | HG03098.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-2024C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528820 | |||||||
chr16:1528858 | A | C | 1 | a0004c0025t0002g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2400-2062T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528858 | |||||||
chr16:1528912 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-2116G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528912 | |||||||
chr16:1528913 | A | G | 89 | a0001c0001t0002g0174 a0001c0001t0004g0170 a0001c0001t0004g0172 others(86): Show |
89 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.2400-2117T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528913 | |||||||
chr16:1528983 | C | T | 34 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(31): Show |
34 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.2400-2187G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528983 | |||||||
chr16:1529010 | T | C | 88 | a0001c0001t0002g0174 a0001c0001t0004g0170 a0001c0001t0004g0172 others(85): Show |
88 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.2400-2214A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529010 | |||||||
chr16:1529142 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2400-2346G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529142 | |||||||
chr16:1529150 | C | T | 87 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(84): Show |
87 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2400-2354G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529150 | |||||||
chr16:1529187 | C | T | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-2391G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529187 | |||||||
chr16:1529203 | G | A | 1 | a0001c0010t0002g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2400-2407C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529203 | |||||||
chr16:1529231 | C | T | 1 | a0017c0055t0004g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2400-2435G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529231 | |||||||
chr16:1529243 | T | C | 2 | a0001c0002t0001g0071 a0001c0002t0001g0095 |
2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2400-2447A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529243 | |||||||
chr16:1529330 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-2534G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529330 | |||||||
chr16:1529458 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2400-2662C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529458 | |||||||
chr16:1529482 | C | T | 111 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0283 others(108): Show |
111 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.2400-2686G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529482 | |||||||
chr16:1529581 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-2785C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529581 | |||||||
chr16:1529740 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2400-2944C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529740 | |||||||
chr16:1529890 | C | T | 4 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-3094G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529890 | |||||||
chr16:1529910 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-3114G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529910 | |||||||
chr16:1530011 | T | C | 3 | a0011c0012t0003g0051 a0011c0012t0003g0052 a0020c0036t0003g0132 |
3 | HG03098.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-3215A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530011 | |||||||
chr16:1530018 | G | A | 7 | a0002c0003t0003g0006 a0002c0003t0003g0030 a0002c0003t0003g0036 others(4): Show |
7 | NA18949.hp1 NA18950.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.2400-3222C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530018 | |||||||
chr16:1530024 | A | G | 80 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(77): Show |
80 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2400-3228T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530024 | |||||||
chr16:1530074 | C | T | 4 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-3278G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530074 | |||||||
chr16:1530119 | T | C | 4 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-3323A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530119 | |||||||
chr16:1530133 | C | CT | 15 | a0001c0001t0002g0235 a0001c0001t0002g0245 a0001c0001t0002g0248 others(12): Show |
15 | HG00621.hp2 HG01123.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.2400-3338dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(4): Show |
2 | a0006c0007t0003g0160 a0006c0007t0003g0164 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2400-3348_2400-333 others(15): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(5): Show |
2 | a0006c0007t0003g0162 a0011c0012t0003g0202 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2400-3349_2400-333 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(6): Show |
4 | a0006c0007t0003g0159 a0006c0007t0003g0161 a0006c0007t0003g0199 others(1): Show |
4 | HG02897.hp2 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-3350_2400-333 others(17): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(7): Show |
1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-3351_2400-333 others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(9): Show |
7 | a0001c0001t0004g0172 a0001c0001t0004g0175 a0001c0001t0004g0229 others(4): Show |
7 | HG02647.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2400-3353_2400-333 others(20): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(10): Show |
12 | a0001c0001t0004g0170 a0003c0005t0001g0142 a0003c0005t0001g0144 others(9): Show |
12 | HG01192.hp1 HG02015.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2400-3354_2400-333 others(21): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(11): Show |
7 | a0001c0004t0001g0084 a0003c0005t0001g0141 a0003c0005t0001g0143 others(4): Show |
7 | HG00099.hp2 HG02056.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.2400-3355_2400-333 others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(12): Show |
2 | a0003c0017t0001g0058 a0003c0018t0001g0133 |
2 | HG01243.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2400-3356_2400-333 others(23): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(13): Show |
2 | a0007c0013t0001g0191 a0007c0013t0001g0192 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2400-3357_2400-333 others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(14): Show |
1 | a0007c0013t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2400-3358_2400-333 others(25): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(15): Show |
1 | a0007c0013t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2400-3359_2400-333 others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | C | CTTTTTTT others(16): Show |
5 | a0003c0005t0001g0147 a0003c0005t0001g0156 a0003c0005t0001g0157 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-3360_2400-333 others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | CT | C | 43 | a0001c0001t0002g0307 a0001c0001t0002g0321 a0001c0002t0001g0197 others(40): Show |
43 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2400-3338delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530133 | CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2400-3349_2400-333 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | |||||||
chr16:1530529 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2400-3733G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530529 | |||||||
chr16:1530530 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2400-3734C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530530 | |||||||
chr16:1530532 | G | A | 1 | a0014c0042t0001g0108 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2400-3736C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530532 | |||||||
chr16:1530579 | T | C | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-3783A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530579 | |||||||
chr16:1530694 | A | ACCCGTGG others(18): Show |
1 | a0019c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2400-3923_2400-389 others(29): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530694 | |||||||
chr16:1530694 | A | ACCCGTGG others(43): Show |
3 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 |
3 | HG02922.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2400-3948_2400-389 others(54): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530694 | |||||||
chr16:1530694 | ACCCGTGG others(18): Show |
A | 2 | a0001c0002t0001g0068 a0001c0004t0003g0189 |
2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2400-3923_2400-389 others(29): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530694 | |||||||
chr16:1530698 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2400-3902C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530698 | |||||||
chr16:1530722 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-3926G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530722 | |||||||
chr16:1530822 | C | T | 1 | a0001c0001t0002g0332 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2400-4026G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530822 | |||||||
chr16:1530823 | G | T | 1 | a0001c0002t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2400-4027C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530823 | |||||||
chr16:1530843 | C | G | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2400-4047G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530843 | |||||||
chr16:1530991 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-4195G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530991 | |||||||
chr16:1531129 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2400-4333C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531129 | |||||||
chr16:1531337 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2400-4541G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531337 | |||||||
chr16:1531347 | CTG | C | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0006c0007t0003g0164 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-4553_2400-455 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531347 | |||||||
chr16:1531506 | C | T | 2 | a0008c0021t0002g0315 a0008c0021t0002g0316 |
2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2400-4710G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531506 | |||||||
chr16:1531519 | C | G | 8 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2400-4723G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531519 | |||||||
chr16:1531769 | A | G | 94 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(91): Show |
94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.2400-4973T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531769 | |||||||
chr16:1531940 | T | C | 1 | a0001c0004t0001g0104 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2400-5144A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531940 | |||||||
chr16:1531959 | C | T | 2 | a0007c0013t0001g0191 a0007c0013t0001g0193 |
2 | HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2400-5163G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531959 | |||||||
chr16:1532087 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-5291C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532087 | |||||||
chr16:1532094 | C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2400-5298G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532094 | |||||||
chr16:1532199 | C | T | 1 | a0005c0049t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2400-5403G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532199 | |||||||
chr16:1532308 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-5512G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532308 | |||||||
chr16:1532319 | C | T | 4 | a0001c0001t0004g0226 a0003c0005t0001g0141 a0003c0005t0001g0142 others(1): Show |
4 | HG02145.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-5523G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532319 | |||||||
chr16:1532394 | G | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-5598C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532394 | |||||||
chr16:1532455 | T | C | 2 | a0001c0001t0002g0174 a0003c0005t0003g0063 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2400-5659A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532455 | |||||||
chr16:1532470 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2400-5674T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532470 | |||||||
chr16:1532645 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-5849C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532645 | |||||||
chr16:1532768 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-5972G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532768 | |||||||
chr16:1532857 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2400-6061G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532857 | |||||||
chr16:1532869 | C | T | 39 | a0001c0001t0002g0174 a0001c0001t0004g0170 a0001c0001t0004g0172 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.2400-6073G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532869 | |||||||
chr16:1532980 | G | A | 1 | a0008c0040t0003g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2400-6184C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532980 | |||||||
chr16:1533015 | C | T | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2400-6219G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533015 | |||||||
chr16:1533050 | TCCTCCAA others(53): Show |
T | 4 | a0001c0002t0001g0103 a0001c0002t0001g0333 a0001c0002t0001g0334 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-6314_2400-625 others(64): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533050 | |||||||
chr16:1533058 | G | T | 9 | a0001c0001t0002g0295 a0001c0001t0003g0038 a0004c0006t0002g0204 others(6): Show |
9 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2400-6262C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533058 | |||||||
chr16:1533059 | T | A | 9 | a0001c0001t0002g0295 a0001c0001t0003g0038 a0004c0006t0002g0204 others(6): Show |
9 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2400-6263A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533059 | |||||||
chr16:1533075 | C | T | 2 | a0001c0001t0002g0174 a0003c0005t0003g0063 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2400-6279G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533075 | |||||||
chr16:1533200 | C | T | 38 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-6404G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533200 | |||||||
chr16:1533228 | T | G | 1 | a0002c0003t0003g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2400-6432A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533228 | |||||||
chr16:1533237 | C | A | 2 | a0001c0001t0007g0265 a0001c0001t0007g0270 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2400-6441G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533237 | |||||||
chr16:1533309 | TCCTATGG others(11): Show |
T | 3 | a0001c0002t0001g0086 a0001c0002t0001g0088 a0001c0002t0001g0091 |
3 | HG00423.hp1 NA18980.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2400-6531_2400-651 others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533309 | |||||||
chr16:1533443 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2400-6647G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533443 | |||||||
chr16:1533463 | G | T | 2 | a0001c0001t0002g0240 a0001c0001t0002g0319 |
2 | NA18957.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2400-6667C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533463 | |||||||
chr16:1533480 | CCT | C | 4 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-6686_2400-668 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533480 | |||||||
chr16:1533492 | G | A | 1 | a0001c0004t0003g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2400-6696C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533492 | |||||||
chr16:1533598 | C | T | 3 | a0001c0002t0001g0196 a0001c0004t0001g0117 a0018c0061t0001g0116 |
3 | HG01884.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2400-6802G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533598 | |||||||
chr16:1533633 | T | C | 93 | a0001c0001t0002g0174 a0001c0001t0004g0170 a0001c0001t0004g0172 others(90): Show |
93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2400-6837A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533633 | |||||||
chr16:1533668 | T | C | 1 | a0004c0006t0002g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2400-6872A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533668 | |||||||
chr16:1533819 | C | T | 1 | a0001c0004t0003g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2400-7023G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533819 | |||||||
chr16:1533876 | C | T | 13 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(10): Show |
13 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2400-7080G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533876 | |||||||
chr16:1534248 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2400-7452G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534248 | |||||||
chr16:1534265 | C | A | 1 | a0001c0001t0002g0250 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2400-7469G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534265 | |||||||
chr16:1534275 | G | T | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2400-7479C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534275 | |||||||
chr16:1534293 | C | T | 8 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2400-7497G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534293 | |||||||
chr16:1534437 | G | C | 4 | a0001c0002t0001g0080 a0001c0002t0001g0106 a0001c0004t0003g0081 others(1): Show |
4 | HG00408.hp2 NA18961.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-7641C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534437 | |||||||
chr16:1534445 | G | C | 39 | a0001c0001t0002g0174 a0001c0001t0004g0170 a0001c0001t0004g0172 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.2400-7649C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534445 | |||||||
chr16:1534515 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-7719G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534515 | |||||||
chr16:1534590 | G | C | 2 | a0001c0002t0001g0128 a0001c0037t0001g0127 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2400-7794C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534590 | |||||||
chr16:1534593 | C | T | 2 | a0006c0007t0003g0161 a0006c0007t0003g0162 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2400-7797G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534593 | |||||||
chr16:1534617 | T | C | 201 | a0001c0001t0002g0174 a0001c0001t0002g0283 a0001c0001t0004g0170 others(198): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2400-7821A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534617 | |||||||
chr16:1534627 | G | A | 38 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-7831C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534627 | |||||||
chr16:1534674 | C | T | 1 | a0003c0005t0001g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2400-7878G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534674 | |||||||
chr16:1534691 | C | T | 7 | a0002c0003t0003g0011 a0002c0003t0003g0016 a0002c0003t0003g0021 others(4): Show |
7 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2400-7895G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534691 | |||||||
chr16:1534846 | G | A | 2 | a0001c0001t0002g0288 a0001c0001t0002g0289 |
2 | HG01099.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2400-8050C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534846 | |||||||
chr16:1534865 | T | C | 203 | a0001c0001t0002g0174 a0001c0001t0002g0283 a0001c0001t0004g0170 others(200): Show |
203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2400-8069A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534865 | |||||||
chr16:1534866 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0070 |
2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2400-8070C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534866 | |||||||
chr16:1534900 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2400-8104G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534900 | |||||||
chr16:1534942 | C | T | 1 | a0001c0002t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2400-8146G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534942 | |||||||
chr16:1534976 | G | A | 1 | a0002c0003t0003g0007 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2400-8180C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534976 | |||||||
chr16:1534983 | C | T | 8 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2400-8187G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534983 | |||||||
chr16:1535100 | G | A | 4 | a0001c0001t0004g0226 a0003c0005t0001g0141 a0003c0005t0001g0142 others(1): Show |
4 | HG02145.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-8304C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535100 | |||||||
chr16:1535113 | C | T | 1 | a0002c0003t0003g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2400-8317G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535113 | |||||||
chr16:1535114 | G | A | 104 | a0001c0001t0002g0283 a0001c0002t0001g0005 a0001c0002t0001g0013 others(101): Show |
104 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2400-8318C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535114 | |||||||
chr16:1535138 | C | T | 1 | a0001c0002t0003g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2400-8342G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535138 | |||||||
chr16:1535380 | G | A | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2400-8584C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535380 | |||||||
chr16:1535438 | G | A | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2400-8642C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535438 | |||||||
chr16:1535455 | A | G | 35 | a0001c0001t0002g0174 a0003c0005t0001g0141 a0003c0005t0001g0142 others(32): Show |
35 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.2400-8659T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535455 | |||||||
chr16:1535553 | G | A | 1 | a0001c0002t0001g0220 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2400-8757C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535553 | |||||||
chr16:1535625 | C | T | 1 | a0001c0001t0002g0323 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2400-8829G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535625 | |||||||
chr16:1535627 | C | T | 3 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 |
3 | HG01891.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2400-8831G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535627 | |||||||
chr16:1535649 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2400-8853T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535649 | |||||||
chr16:1535891 | T | C | 2 | a0001c0002t0001g0041 a0001c0054t0001g0119 |
2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2400-9095A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535891 | |||||||
chr16:1535927 | C | T | 29 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(26): Show |
29 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.2400-9131G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535927 | |||||||
chr16:1536007 | C | CG | 5 | a0001c0001t0002g0268 a0001c0002t0001g0079 a0001c0004t0001g0084 others(2): Show |
5 | HG02055.hp2 HG02056.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-9212dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536007 | |||||||
chr16:1536153 | A | G | 4 | a0001c0001t0002g0290 a0001c0001t0002g0294 a0001c0001t0002g0296 others(1): Show |
4 | NA18962.hp2 NA18991.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-9357T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536153 | |||||||
chr16:1536220 | G | A | 2 | a0001c0001t0002g0259 a0002c0003t0003g0034 |
2 | HG01261.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2400-9424C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536220 | |||||||
chr16:1536254 | G | A | 69 | a0001c0001t0002g0174 a0002c0003t0003g0006 a0002c0003t0003g0007 others(66): Show |
69 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.2400-9458C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536254 | |||||||
chr16:1536274 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2400-9478G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536274 | |||||||
chr16:1536308 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-9512G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536308 | |||||||
chr16:1536405 | G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2400-9609C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536405 | |||||||
chr16:1536595 | C | T | 38 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-9799G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536595 | |||||||
chr16:1536716 | C | G | 120 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2400-9920G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536716 | |||||||
chr16:1536820 | G | A | 38 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-10024C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536820 | |||||||
chr16:1537028 | C | T | 2 | a0001c0020t0003g0138 a0001c0020t0003g0139 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2400-10232G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537028 | |||||||
chr16:1537066 | T | C | 1 | a0001c0001t0002g0329 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2400-10270A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537066 | |||||||
chr16:1537150 | A | G | 1 | a0001c0001t0002g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2400-10354T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537150 | |||||||
chr16:1537184 | AGCCAGGG others(34): Show |
A | 1 | a0010c0015t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2400-10429_2400-10 others(47): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537184 | |||||||
chr16:1537210 | G | A | 2 | a0001c0001t0002g0174 a0003c0005t0003g0063 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2400-10414C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537210 | |||||||
chr16:1537214 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-10418G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537214 | |||||||
chr16:1537232 | G | T | 2 | a0001c0010t0001g0126 a0001c0010t0002g0322 |
2 | NA18970.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.2400-10436C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537232 | |||||||
chr16:1537276 | C | T | 191 | a0001c0001t0002g0174 a0001c0002t0001g0005 a0001c0002t0001g0013 others(188): Show |
191 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2400-10480G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537276 | |||||||
chr16:1537321 | G | A | 189 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(186): Show |
189 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2400-10525C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537321 | |||||||
chr16:1537510 | G | A | 114 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.2400-10714C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537510 | |||||||
chr16:1537725 | C | T | 4 | a0001c0002t0001g0068 a0001c0002t0001g0073 a0001c0004t0003g0189 others(1): Show |
4 | HG02630.hp1 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-10929G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537725 | |||||||
chr16:1537841 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0070 |
2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2400-11045G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537841 | |||||||
chr16:1537937 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.2400-11141G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537937 | |||||||
chr16:1537978 | G | A | 3 | a0001c0002t0001g0086 a0001c0002t0001g0088 a0001c0002t0001g0091 |
3 | HG00423.hp1 NA18980.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2400-11182C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537978 | |||||||
chr16:1537992 | C | T | 1 | a0003c0005t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2400-11196G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537992 | |||||||
chr16:1538071 | G | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-11275C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538071 | |||||||
chr16:1538086 | A | G | 201 | a0001c0001t0002g0174 a0001c0001t0002g0227 a0001c0001t0002g0232 others(198): Show |
201 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2400-11290T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538086 | |||||||
chr16:1538088 | T | C | 3 | a0001c0004t0003g0078 a0001c0004t0003g0087 a0001c0004t0003g0100 |
3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2400-11292A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538088 | |||||||
chr16:1538112 | C | T | 2 | a0001c0002t0001g0072 a0001c0002t0001g0079 |
2 | NA19010.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2400-11316G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538112 | |||||||
chr16:1538113 | T | C | 3 | a0001c0001t0002g0240 a0001c0001t0002g0319 a0001c0001t0002g0321 |
3 | HG03491.hp1 NA18957.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2400-11317A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538113 | |||||||
chr16:1538127 | A | G | 1 | a0001c0001t0002g0310 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2400-11331T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538127 | |||||||
chr16:1538165 | C | T | 8 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-11369G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538165 | |||||||
chr16:1538179 | C | T | 3 | a0003c0005t0001g0143 a0003c0005t0001g0144 a0003c0005t0001g0145 |
3 | NA18948.hp2 NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2400-11383G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538179 | |||||||
chr16:1538314 | C | T | 1 | a0001c0001t0002g0314 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2400-11518G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538314 | |||||||
chr16:1538438 | C | T | 1 | a0001c0001t0002g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2400-11642G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538438 | |||||||
chr16:1538446 | T | C | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-11650A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538446 | |||||||
chr16:1538708 | C | T | 1 | a0001c0002t0001g0223 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2400-11912G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538708 | |||||||
chr16:1538799 | G | A | 106 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2400-12003C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538799 | |||||||
chr16:1538848 | C | T | 106 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2400-12052G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538848 | |||||||
chr16:1539004 | C | T | 1 | a0001c0002t0001g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2400-12208G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539004 | |||||||
chr16:1539082 | G | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-12286C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539082 | |||||||
chr16:1539187 | T | C | 2 | a0003c0005t0003g0151 a0028c0029t0003g0188 |
2 | HG00609.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2400-12391A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539187 | |||||||
chr16:1539220 | A | C | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12424T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539220 | |||||||
chr16:1539225 | A | C | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12429T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539225 | |||||||
chr16:1539230 | C | T | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12434G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539230 | |||||||
chr16:1539231 | A | G | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12435T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539231 | |||||||
chr16:1539234 | A | C | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12438T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539234 | |||||||
chr16:1539571 | C | T | 3 | a0001c0004t0003g0087 a0001c0004t0003g0100 a0003c0059t0001g0050 |
3 | HG00639.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2400-12775G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539571 | |||||||
chr16:1539792 | G | A | 4 | a0005c0009t0004g0166 a0005c0009t0004g0173 a0005c0049t0004g0171 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-12996C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539792 | |||||||
chr16:1539902 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2400-13106C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539902 | |||||||
chr16:1540088 | G | C | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2400-13292C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540088 | |||||||
chr16:1540110 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2400-13314G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540110 | |||||||
chr16:1540117 | G | A | 1 | a0001c0057t0003g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2400-13321C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540117 | |||||||
chr16:1540167 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2400-13371C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540167 | |||||||
chr16:1540181 | C | A | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2400-13385G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540181 | |||||||
chr16:1540436 | C | G | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2400-13640G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540436 | |||||||
chr16:1540513 | C | T | 1 | a0001c0001t0002g0319 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2400-13717G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540513 | |||||||
chr16:1540575 | C | G | 193 | a0001c0001t0002g0274 a0001c0001t0002g0288 a0001c0001t0002g0289 others(190): Show |
193 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.2400-13779G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540575 | |||||||
chr16:1540666 | C | T | 2 | a0001c0002t0001g0013 a0001c0002t0001g0083 |
2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2400-13870G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540666 | |||||||
chr16:1540670 | C | T | 1 | a0018c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2400-13874G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540670 | |||||||
chr16:1540671 | G | A | 68 | a0001c0001t0002g0274 a0002c0003t0003g0006 a0002c0003t0003g0007 others(65): Show |
68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2400-13875C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540671 | |||||||
chr16:1540680 | C | T | 1 | a0022c0028t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2400-13884G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540680 | |||||||
chr16:1540788 | C | T | 1 | a0001c0004t0003g0014 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2400-13992G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540788 | |||||||
chr16:1541013 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-14217C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541013 | |||||||
chr16:1541111 | G | T | 191 | a0001c0001t0002g0274 a0001c0002t0001g0005 a0001c0002t0001g0013 others(188): Show |
191 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2400-14315C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541111 | |||||||
chr16:1541283 | G | A | 2 | a0001c0001t0002g0304 a0001c0001t0002g0307 |
2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2400-14487C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541283 | |||||||
chr16:1541448 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2400-14652G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541448 | |||||||
chr16:1541591 | G | A | 107 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2400-14795C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541591 | |||||||
chr16:1541749 | G | A | 3 | a0011c0012t0003g0051 a0011c0012t0003g0052 a0020c0036t0003g0132 |
3 | HG03098.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-14953C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541749 | |||||||
chr16:1541861 | C | T | 1 | a0028c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2400-15065G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541861 | |||||||
chr16:1541961 | G | A | 116 | a0001c0001t0002g0277 a0001c0002t0001g0005 a0001c0002t0001g0013 others(113): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2400-15165C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541961 | |||||||
chr16:1542086 | T | C | 123 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(120): Show |
123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.2400-15290A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542086 | |||||||
chr16:1542265 | A | T | 195 | a0001c0001t0002g0274 a0001c0002t0001g0005 a0001c0002t0001g0013 others(192): Show |
195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2400-15469T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542265 | |||||||
chr16:1542314 | C | T | 1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2400-15518G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542314 | |||||||
chr16:1542366 | G | A | 68 | a0001c0001t0002g0274 a0002c0003t0003g0006 a0002c0003t0003g0007 others(65): Show |
68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2399+15569C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542366 | |||||||
chr16:1542384 | T | G | 1 | a0031c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2399+15551A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542384 | |||||||
chr16:1542523 | C | T | 115 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2399+15412G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542523 | |||||||
chr16:1542634 | G | A | 1 | a0031c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2399+15301C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542634 | |||||||
chr16:1542778 | C | T | 7 | a0001c0002t0001g0113 a0001c0004t0001g0084 a0001c0004t0003g0112 others(4): Show |
7 | HG02056.hp1 HG02083.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2399+15157G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542778 | |||||||
chr16:1542789 | T | C | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2399+15146A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542789 | |||||||
chr16:1542850 | G | A | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2399+15085C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542850 | |||||||
chr16:1542856 | G | C | 68 | a0001c0001t0002g0274 a0002c0003t0003g0006 a0002c0003t0003g0007 others(65): Show |
68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2399+15079C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542856 | |||||||
chr16:1543003 | G | A | 115 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2399+14932C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543003 | |||||||
chr16:1543107 | G | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+14828C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543107 | |||||||
chr16:1543110 | C | T | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2399+14825G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543110 | |||||||
chr16:1543170 | A | G | 190 | a0001c0001t0002g0274 a0001c0002t0001g0005 a0001c0002t0001g0013 others(187): Show |
190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2399+14765T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543170 | |||||||
chr16:1543238 | T | C | 1 | a0001c0002t0001g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2399+14697A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543238 | |||||||
chr16:1543279 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2399+14656A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543279 | |||||||
chr16:1543353 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+14582C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543353 | |||||||
chr16:1543432 | G | A | 2 | a0003c0019t0003g0136 a0003c0019t0003g0137 |
2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2399+14503C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543432 | |||||||
chr16:1543488 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2399+14447C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543488 | |||||||
chr16:1543605 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+14330G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543605 | |||||||
chr16:1543619 | G | A | 1 | a0001c0048t0002g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2399+14316C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543619 | |||||||
chr16:1543644 | C | T | 263 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0180 others(260): Show |
263 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.2399+14291G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543644 | |||||||
chr16:1543689 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2399+14246G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543689 | |||||||
chr16:1543842 | G | A | 108 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2399+14093C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543842 | |||||||
chr16:1543862 | C | T | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+14073G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543862 | |||||||
chr16:1543958 | A | C | 1 | a0001c0050t0002g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2399+13977T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543958 | |||||||
chr16:1544019 | C | CT | 11 | a0001c0001t0002g0252 a0001c0001t0002g0259 a0001c0001t0002g0264 others(8): Show |
11 | HG00423.hp2 HG01069.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+13915dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544019 | |||||||
chr16:1544157 | G | A | 190 | a0001c0001t0002g0274 a0001c0002t0001g0005 a0001c0002t0001g0013 others(187): Show |
190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2399+13778C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544157 | |||||||
chr16:1544160 | G | T | 117 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(114): Show |
117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2399+13775C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544160 | |||||||
chr16:1544161 | GCACCTGC | G | 5 | a0008c0046t0004g0258 a0009c0011t0003g0042 a0009c0011t0003g0043 others(2): Show |
5 | HG01192.hp2 HG01257.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2399+13767_2399+13 others(13): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544161 | |||||||
chr16:1544184 | AT | A | 7 | a0001c0001t0002g0233 a0001c0001t0002g0255 a0001c0002t0001g0190 others(4): Show |
7 | HG03017.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2399+13750delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544184 | |||||||
chr16:1544217 | T | A | 28 | a0001c0001t0002g0274 a0003c0005t0001g0141 a0003c0005t0001g0142 others(25): Show |
28 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.2399+13718A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544217 | |||||||
chr16:1544247 | A | G | 124 | a0001c0001t0002g0237 a0001c0002t0001g0005 a0001c0002t0001g0013 others(121): Show |
124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2399+13688T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544247 | |||||||
chr16:1544276 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13659G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544276 | |||||||
chr16:1544313 | A | G | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+13622T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544313 | |||||||
chr16:1544338 | C | A | 1 | a0001c0002t0001g0091 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2399+13597G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544338 | |||||||
chr16:1544340 | T | C | 6 | a0001c0002t0001g0047 a0001c0002t0001g0082 a0001c0002t0001g0096 others(3): Show |
6 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+13595A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544340 | |||||||
chr16:1544350 | A | AT | 10 | a0001c0001t0002g0295 a0001c0001t0003g0038 a0004c0006t0002g0204 others(7): Show |
10 | HG00733.hp2 HG00741.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2399+13584dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544350 | |||||||
chr16:1544375 | T | C | 33 | a0001c0001t0002g0274 a0003c0005t0001g0141 a0003c0005t0001g0142 others(30): Show |
33 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2399+13560A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544375 | |||||||
chr16:1544407 | G | C | 1 | a0002c0003t0003g0026 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2399+13528C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544407 | |||||||
chr16:1544420 | C | T | 1 | a0001c0014t0003g0102 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2399+13515G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544420 | |||||||
chr16:1544475 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2399+13460C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544475 | |||||||
chr16:1544671 | T | C | 2 | a0001c0001t0002g0244 a0004c0026t0004g0312 |
2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2399+13264A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544671 | |||||||
chr16:1544682 | C | T | 2 | a0001c0001t0002g0244 a0004c0026t0004g0312 |
2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2399+13253G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544682 | |||||||
chr16:1544687 | G | C | 2 | a0001c0001t0002g0244 a0004c0026t0004g0312 |
2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2399+13248C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544687 | |||||||
chr16:1544718 | G | A | 5 | a0001c0002t0001g0005 a0001c0002t0001g0066 a0001c0002t0001g0072 others(2): Show |
5 | NA18966.hp2 NA18970.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+13217C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544718 | |||||||
chr16:1544734 | C | T | 1 | a0031c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2399+13201G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544734 | |||||||
chr16:1544738 | T | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13197A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544738 | |||||||
chr16:1544741 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13194G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544741 | |||||||
chr16:1544766 | A | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13169T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544766 | |||||||
chr16:1544794 | A | G | 2 | a0003c0005t0003g0063 a0003c0018t0001g0133 |
2 | HG04204.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2399+13141T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544794 | |||||||
chr16:1544800 | C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2399+13135G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544800 | |||||||
chr16:1544807 | CCTGG | C | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+13124_2399+13 others(10): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544807 | |||||||
chr16:1544809 | T | C | 2 | a0001c0001t0002g0234 a0003c0018t0001g0133 |
2 | HG04204.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.2399+13126A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544809 | |||||||
chr16:1544895 | G | A | 1 | a0001c0001t0007g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2399+13040C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544895 | |||||||
chr16:1544899 | C | T | 1 | a0023c0030t0003g0198 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2399+13036G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544899 | |||||||
chr16:1544925 | A | G | 19 | a0001c0001t0002g0274 a0003c0005t0001g0141 a0003c0005t0001g0142 others(16): Show |
19 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.2399+13010T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544925 | |||||||
chr16:1544936 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2399+12999G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544936 | |||||||
chr16:1544943 | C | T | 35 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(32): Show |
35 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2399+12992G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544943 | |||||||
chr16:1545026 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2399+12909C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545026 | |||||||
chr16:1545072 | A | C | 2 | a0001c0002t0001g0333 a0001c0002t0001g0334 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2399+12863T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545072 | |||||||
chr16:1545124 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+12811C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545124 | |||||||
chr16:1545504 | T | C | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2399+12431A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545504 | |||||||
chr16:1545514 | GT | G | 9 | a0002c0003t0003g0008 a0006c0007t0003g0159 a0006c0007t0003g0160 others(6): Show |
9 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2399+12420delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545514 | |||||||
chr16:1545530 | T | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+12405A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545530 | |||||||
chr16:1545532 | G | A | 3 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0009 |
3 | NA18941.hp1 NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2399+12403C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545532 | |||||||
chr16:1545599 | C | T | 26 | a0001c0001t0002g0274 a0003c0005t0001g0141 a0003c0005t0001g0142 others(23): Show |
26 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.2399+12336G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545599 | |||||||
chr16:1545815 | T | G | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2399+12120A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545815 | |||||||
chr16:1546122 | G | A | 5 | a0001c0002t0001g0086 a0001c0002t0001g0088 a0001c0002t0001g0091 others(2): Show |
5 | HG00423.hp1 HG00673.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+11813C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546122 | |||||||
chr16:1546226 | C | G | 1 | a0001c0001t0002g0274 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2399+11709G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546226 | |||||||
chr16:1546258 | C | T | 34 | a0001c0002t0001g0005 a0001c0002t0001g0061 a0001c0002t0001g0066 others(31): Show |
34 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.2399+11677G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546258 | |||||||
chr16:1546515 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+11420C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546515 | |||||||
chr16:1546532 | G | T | 1 | a0001c0004t0003g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2399+11403C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546532 | |||||||
chr16:1546559 | T | C | 2 | a0003c0019t0003g0136 a0003c0019t0003g0137 |
2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2399+11376A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546559 | |||||||
chr16:1546885 | G | A | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2399+11050C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546885 | |||||||
chr16:1547209 | C | T | 63 | a0001c0001t0002g0274 a0002c0003t0003g0006 a0002c0003t0003g0007 others(60): Show |
63 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2399+10726G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547209 | |||||||
chr16:1547271 | C | T | 2 | a0001c0002t0001g0128 a0001c0037t0001g0127 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2399+10664G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547271 | |||||||
chr16:1547272 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2399+10663C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547272 | |||||||
chr16:1547278 | A | G | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+10657T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547278 | |||||||
chr16:1547375 | C | T | 3 | a0003c0005t0001g0143 a0003c0005t0001g0144 a0003c0005t0001g0145 |
3 | NA18948.hp2 NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2399+10560G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547375 | |||||||
chr16:1547376 | G | A | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2399+10559C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547376 | |||||||
chr16:1547575 | T | C | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+10360A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547575 | |||||||
chr16:1547624 | C | T | 1 | a0002c0003t0003g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2399+10311G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547624 | |||||||
chr16:1547759 | C | A | 1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2399+10176G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547759 | |||||||
chr16:1547800 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2399+10135G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547800 | |||||||
chr16:1547813 | G | A | 63 | a0001c0001t0002g0274 a0002c0003t0003g0006 a0002c0003t0003g0007 others(60): Show |
63 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2399+10122C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547813 | |||||||
chr16:1547876 | C | T | 28 | a0001c0001t0002g0274 a0003c0005t0001g0141 a0003c0005t0001g0142 others(25): Show |
28 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.2399+10059G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547876 | |||||||
chr16:1547923 | C | T | 111 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2399+10012G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547923 | |||||||
chr16:1548090 | C | A | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2399+9845G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548090 | |||||||
chr16:1548090 | C | T | 1 | a0001c0001t0002g0319 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2399+9845G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548090 | |||||||
chr16:1548270 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2399+9665C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548270 | |||||||
chr16:1548318 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+9617C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548318 | |||||||
chr16:1548719 | C | G | 1 | a0001c0001t0002g0254 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2399+9216G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548719 | |||||||
chr16:1548762 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+9173G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548762 | |||||||
chr16:1548775 | G | A | 1 | a0001c0002t0001g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2399+9160C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548775 | |||||||
chr16:1548779 | T | C | 1 | a0008c0046t0004g0258 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2399+9156A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548779 | |||||||
chr16:1548814 | C | T | 4 | a0001c0001t0002g0282 a0001c0001t0002g0285 a0001c0001t0002g0332 others(1): Show |
4 | HG02155.hp1 HG02165.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+9121G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548814 | |||||||
chr16:1549145 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+8790G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549145 | |||||||
chr16:1549480 | G | A | 14 | a0002c0003t0003g0006 a0002c0003t0003g0017 a0002c0003t0003g0019 others(11): Show |
14 | NA18949.hp1 NA18950.hp2 NA18961.hp1 others(11): Show |
intron_variant | MODIFIER | c.2399+8455C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549480 | |||||||
chr16:1549489 | T | C | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+8446A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549489 | |||||||
chr16:1549498 | G | A | 1 | a0002c0003t0003g0032 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2399+8437C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549498 | |||||||
chr16:1549574 | G | A | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2399+8361C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549574 | |||||||
chr16:1549589 | G | A | 2 | a0001c0001t0002g0228 a0021c0047t0002g0287 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2399+8346C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549589 | |||||||
chr16:1549912 | G | A | 117 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(114): Show |
117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2399+8023C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549912 | |||||||
chr16:1550025 | G | A | 2 | a0001c0002t0001g0080 a0001c0004t0003g0081 |
2 | NA18961.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2399+7910C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550025 | |||||||
chr16:1550136 | C | T | 107 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2399+7799G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550136 | |||||||
chr16:1550141 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+7794A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550141 | |||||||
chr16:1550251 | A | G | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2399+7684T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550251 | |||||||
chr16:1550271 | T | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+7664A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550271 | |||||||
chr16:1550338 | A | T | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+7597T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550338 | |||||||
chr16:1550737 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+7198C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550737 | |||||||
chr16:1550844 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+7091G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550844 | |||||||
chr16:1550881 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2399+7054C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550881 | |||||||
chr16:1551286 | A | G | 193 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(190): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+6649T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551286 | |||||||
chr16:1551330 | C | A | 157 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(154): Show |
157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2399+6605G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551330 | |||||||
chr16:1551461 | C | T | 1 | a0002c0003t0003g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2399+6474G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551461 | |||||||
chr16:1551494 | T | C | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2399+6441A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551494 | |||||||
chr16:1551682 | C | T | 1 | a0001c0002t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2399+6253G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551682 | |||||||
chr16:1551701 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+6234G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551701 | |||||||
chr16:1551766 | T | C | 157 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(154): Show |
157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2399+6169A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551766 | |||||||
chr16:1551769 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2399+6166C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551769 | |||||||
chr16:1551799 | T | C | 1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2399+6136A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551799 | |||||||
chr16:1551815 | C | T | 33 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(30): Show |
33 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2399+6120G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551815 | |||||||
chr16:1551816 | G | A | 1 | a0001c0004t0003g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2399+6119C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551816 | |||||||
chr16:1551853 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+6082G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551853 | |||||||
chr16:1551878 | A | G | 194 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(191): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+6057T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551878 | |||||||
chr16:1552034 | C | T | 15 | a0001c0001t0002g0179 a0001c0001t0002g0239 a0001c0001t0002g0271 others(12): Show |
15 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.2399+5901G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552034 | |||||||
chr16:1552035 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2399+5900C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552035 | |||||||
chr16:1552113 | C | A | 34 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+5822G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552113 | |||||||
chr16:1552259 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+5676G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552259 | |||||||
chr16:1552322 | T | C | 76 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2399+5613A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552322 | |||||||
chr16:1552426 | A | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+5509T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552426 | |||||||
chr16:1552577 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2399+5358C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552577 | |||||||
chr16:1552593 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+5342C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552593 | |||||||
chr16:1552607 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+5328C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552607 | |||||||
chr16:1552648 | C | CT | 152 | a0001c0001t0002g0277 a0001c0001t0007g0265 a0001c0002t0001g0005 others(149): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.2399+5286dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552648 | |||||||
chr16:1552709 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2399+5226G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552709 | |||||||
chr16:1552737 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2399+5198G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552737 | |||||||
chr16:1552810 | A | G | 193 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(190): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+5125T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552810 | |||||||
chr16:1552844 | A | G | 197 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(194): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2399+5091T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552844 | |||||||
chr16:1552937 | A | G | 193 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(190): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+4998T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552937 | |||||||
chr16:1553013 | A | C | 1 | a0001c0001t0007g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2399+4922T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553013 | |||||||
chr16:1553041 | A | G | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+4894T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553041 | |||||||
chr16:1553068 | A | T | 1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2399+4867T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553068 | |||||||
chr16:1553330 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2399+4605C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553330 | |||||||
chr16:1553495 | C | T | 4 | a0001c0001t0002g0317 a0001c0001t0002g0320 a0008c0021t0002g0315 others(1): Show |
4 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+4440G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553495 | |||||||
chr16:1553517 | G | C | 1 | a0001c0004t0001g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2399+4418C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553517 | |||||||
chr16:1553534 | T | C | 194 | a0001c0001t0002g0277 a0001c0002t0001g0005 a0001c0002t0001g0013 others(191): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+4401A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553534 | |||||||
chr16:1553575 | G | A | 194 | a0001c0001t0002g0277 a0001c0002t0001g0005 a0001c0002t0001g0013 others(191): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+4360C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553575 | |||||||
chr16:1553715 | C | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+4220G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553715 | |||||||
chr16:1553887 | T | C | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2399+4048A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553887 | |||||||
chr16:1553953 | C | T | 1 | a0001c0004t0003g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2399+3982G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553953 | |||||||
chr16:1554051 | A | G | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+3884T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554051 | |||||||
chr16:1554387 | G | A | 117 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(114): Show |
117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2399+3548C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554387 | |||||||
chr16:1554526 | C | T | 3 | a0001c0014t0003g0102 a0001c0014t0006g0209 a0001c0014t0006g0215 |
3 | HG02080.hp1 HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2399+3409G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554526 | |||||||
chr16:1554655 | C | T | 2 | a0001c0002t0001g0333 a0001c0002t0001g0334 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2399+3280G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554655 | |||||||
chr16:1554700 | T | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+3235A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554700 | |||||||
chr16:1555008 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2399+2927G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555008 | |||||||
chr16:1555043 | C | T | 31 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.2399+2892G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555043 | |||||||
chr16:1555049 | C | T | 1 | a0006c0007t0003g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2399+2886G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555049 | |||||||
chr16:1555050 | A | G | 198 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(195): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2399+2885T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555050 | |||||||
chr16:1555052 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+2883G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555052 | |||||||
chr16:1555162 | C | A | 108 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2399+2773G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555162 | |||||||
chr16:1555216 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2399+2719C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555216 | |||||||
chr16:1555233 | T | C | 1 | a0001c0004t0001g0104 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2399+2702A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555233 | |||||||
chr16:1555270 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2399+2665G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555270 | |||||||
chr16:1555384 | G | A | 1 | a0002c0003t0003g0022 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2399+2551C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555384 | |||||||
chr16:1555536 | T | C | 194 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(191): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+2399A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555536 | |||||||
chr16:1555605 | C | T | 118 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.2399+2330G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555605 | |||||||
chr16:1555866 | G | A | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2399+2069C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555866 | |||||||
chr16:1555974 | C | T | 34 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+1961G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555974 | |||||||
chr16:1556129 | A | T | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2399+1806T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556129 | |||||||
chr16:1556148 | C | T | 3 | a0001c0002t0001g0196 a0001c0004t0001g0117 a0018c0061t0001g0116 |
3 | HG01884.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2399+1787G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556148 | |||||||
chr16:1556160 | T | A | 1 | a0001c0001t0002g0317 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2399+1775A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556160 | |||||||
chr16:1556166 | A | G | 34 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+1769T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556166 | |||||||
chr16:1556335 | C | T | 4 | a0001c0002t0001g0069 a0001c0002t0001g0197 a0001c0002t0010g0186 others(1): Show |
4 | HG00621.hp2 NA18962.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+1600G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556335 | |||||||
chr16:1556443 | A | G | 193 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(190): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+1492T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556443 | |||||||
chr16:1556444 | A | G | 193 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(190): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+1491T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556444 | |||||||
chr16:1556478 | C | T | 34 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+1457G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556478 | |||||||
chr16:1556479 | C | T | 1 | a0003c0005t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2399+1456G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556479 | |||||||
chr16:1556608 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2399+1327T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556608 | |||||||
chr16:1556731 | CT | C | 3 | a0001c0004t0003g0078 a0001c0004t0003g0087 a0001c0004t0003g0100 |
3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2399+1203delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556731 | |||||||
chr16:1556731 | CTTTTTTA others(16): Show |
C | 1 | a0002c0003t0003g0032 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2399+1181_2399+120 others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556731 | |||||||
chr16:1556733 | T | A | 3 | a0001c0004t0003g0078 a0001c0004t0003g0087 a0001c0004t0003g0100 |
3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2399+1202A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556733 | |||||||
chr16:1556738 | A | G | 107 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2399+1197T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556738 | |||||||
chr16:1556786 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+1149G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556786 | |||||||
chr16:1556803 | T | G | 1 | a0001c0002t0001g0083 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2399+1132A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556803 | |||||||
chr16:1556844 | C | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0266 a0001c0001t0002g0267 others(2): Show |
5 | HG02738.hp1 HG03239.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+1091G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556844 | |||||||
chr16:1557112 | GC | G | 70 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.2399+822delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557112 | |||||||
chr16:1557164 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2399+771C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557164 | |||||||
chr16:1557241 | C | T | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2399+694G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557241 | |||||||
chr16:1557283 | G | T | 35 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(32): Show |
35 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2399+652C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557283 | |||||||
chr16:1557285 | G | C | 36 | a0001c0001t0002g0289 a0001c0002t0001g0128 a0001c0037t0001g0127 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+650C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557285 | |||||||
chr16:1557382 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+553C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557382 | |||||||
chr16:1557449 | C | G | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+486G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557449 | |||||||
chr16:1557454 | T | G | 1 | a0001c0002t0001g0088 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2399+481A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557454 | |||||||
chr16:1557528 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2399+407C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557528 | |||||||
chr16:1557548 | A | G | 1 | a0018c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2399+387T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557548 | |||||||
chr16:1557563 | T | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+372A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557563 | |||||||
chr16:1557573 | C | T | 194 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(191): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+362G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557573 | |||||||
chr16:1557703 | G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2399+232C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557703 | |||||||
chr16:1557826 | C | G | 1 | a0016c0038t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2399+109G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557826 | |||||||
chr16:1558176 | A | G | 160 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(157): Show |
160 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2200-42T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558176 | |||||||
chr16:1558201 | G | A | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2200-67C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558201 | |||||||
chr16:1558363 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-229C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558363 | |||||||
chr16:1558706 | G | C | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2200-572C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558706 | |||||||
chr16:1558728 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-594C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558728 | |||||||
chr16:1558845 | G | C | 2 | a0001c0002t0003g0090 a0001c0002t0003g0105 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2200-711C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558845 | |||||||
chr16:1558885 | C | G | 3 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0009 |
3 | NA18941.hp1 NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2200-751G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558885 | |||||||
chr16:1558904 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2200-770C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558904 | |||||||
chr16:1558933 | A | G | 194 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(191): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2200-799T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558933 | |||||||
chr16:1559115 | C | T | 2 | a0001c0002t0001g0085 a0025c0024t0001g0111 |
2 | NA18973.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2200-981G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559115 | |||||||
chr16:1559134 | T | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-1000A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559134 | |||||||
chr16:1559205 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2200-1071G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559205 | |||||||
chr16:1559506 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2200-1372C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559506 | |||||||
chr16:1559539 | G | A | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2200-1405C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559539 | |||||||
chr16:1559623 | C | A | 1 | a0001c0002t0010g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2200-1489G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559623 | |||||||
chr16:1559754 | G | C | 1 | a0002c0003t0003g0015 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2200-1620C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559754 | |||||||
chr16:1559794 | C | T | 1 | a0019c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2200-1660G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559794 | |||||||
chr16:1559842 | G | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-1708C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559842 | |||||||
chr16:1559852 | C | T | 2 | a0001c0020t0003g0138 a0001c0020t0003g0139 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2200-1718G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559852 | |||||||
chr16:1559907 | C | T | 1 | a0002c0003t0003g0023 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2200-1773G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559907 | |||||||
chr16:1559940 | G | A | 1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2200-1806C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559940 | |||||||
chr16:1559943 | C | T | 4 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0302 others(1): Show |
4 | HG01099.hp1 HG01433.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2200-1809G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559943 | |||||||
chr16:1560008 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2200-1874G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560008 | |||||||
chr16:1560175 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2199+1810C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560175 | |||||||
chr16:1560214 | C | G | 70 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.2199+1771G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560214 | |||||||
chr16:1560366 | C | T | 7 | a0001c0002t0001g0113 a0001c0004t0001g0084 a0001c0004t0003g0112 others(4): Show |
7 | HG02056.hp1 HG02083.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2199+1619G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560366 | |||||||
chr16:1560380 | C | T | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2199+1605G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560380 | |||||||
chr16:1560497 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2199+1488G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560497 | |||||||
chr16:1560577 | G | A | 2 | a0001c0001t0007g0265 a0001c0001t0007g0270 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2199+1408C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560577 | |||||||
chr16:1560718 | C | A | 2 | a0011c0012t0003g0201 a0011c0012t0003g0202 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2199+1267G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560718 | |||||||
chr16:1560783 | A | G | 1 | a0001c0002t0001g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2199+1202T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560783 | |||||||
chr16:1560884 | A | G | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2199+1101T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560884 | |||||||
chr16:1560985 | T | C | 5 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2199+1000A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560985 | |||||||
chr16:1561053 | G | A | 1 | a0001c0001t0004g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2199+932C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561053 | |||||||
chr16:1561067 | G | A | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2199+918C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561067 | |||||||
chr16:1561154 | G | A | 1 | a0001c0010t0004g0238 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2199+831C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561154 | |||||||
chr16:1561187 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2199+798G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561187 | |||||||
chr16:1561273 | C | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2199+712G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561273 | |||||||
chr16:1561362 | T | A | 2 | a0011c0012t0003g0201 a0011c0012t0003g0202 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2199+623A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561362 | |||||||
chr16:1561497 | G | A | 4 | a0006c0007t0003g0159 a0006c0007t0003g0161 a0006c0007t0003g0162 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2199+488C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561497 | |||||||
chr16:1561825 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2199+160G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561825 | |||||||
chr16:1561949 | T | A | 3 | a0001c0002t0001g0196 a0001c0004t0001g0117 a0018c0061t0001g0116 |
3 | HG01884.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2199+36A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561949 | |||||||
chr16:1562144 | G | GT | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068-29dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562144 | |||||||
chr16:1562205 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2068-89G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562205 | |||||||
chr16:1562219 | C | T | 1 | a0001c0002t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2068-103G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562219 | |||||||
chr16:1562379 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2068-263T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562379 | |||||||
chr16:1562458 | C | T | 2 | a0001c0001t0002g0228 a0021c0047t0002g0287 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2068-342G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562458 | |||||||
chr16:1562492 | G | A | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068-376C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562492 | |||||||
chr16:1562497 | C | G | 34 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2068-381G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562497 | |||||||
chr16:1562623 | T | A | 2 | a0001c0001t0002g0261 a0001c0050t0002g0328 |
2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2068-507A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562623 | |||||||
chr16:1562639 | G | A | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2068-523C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562639 | |||||||
chr16:1562881 | T | C | 1 | a0005c0049t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2068-765A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562881 | |||||||
chr16:1563038 | A | G | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.2068-922T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563038 | |||||||
chr16:1563296 | CT | C | 31 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0009 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.2067+700delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563296 | |||||||
chr16:1563308 | C | T | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+689G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563308 | |||||||
chr16:1563309 | T | C | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+688A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563309 | |||||||
chr16:1563347 | A | G | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2067+650T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563347 | |||||||
chr16:1563364 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2067+633C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563364 | |||||||
chr16:1563374 | G | A | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+623C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563374 | |||||||
chr16:1563407 | T | C | 1 | a0002c0003t0003g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2067+590A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563407 | |||||||
chr16:1563423 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+574T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563423 | |||||||
chr16:1563427 | T | C | 5 | a0001c0001t0002g0228 a0001c0001t0002g0253 a0001c0001t0002g0301 others(2): Show |
5 | HG02257.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2067+570A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563427 | |||||||
chr16:1563431 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2067+566G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563431 | |||||||
chr16:1563432 | G | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+565C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563432 | |||||||
chr16:1563439 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+558T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563439 | |||||||
chr16:1563450 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+547T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563450 | |||||||
chr16:1563451 | A | G | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+546T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563451 | |||||||
chr16:1563452 | A | T | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+545T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563452 | |||||||
chr16:1563454 | A | T | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+543T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563454 | |||||||
chr16:1563455 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+542T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563455 | |||||||
chr16:1563457 | C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+540G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563457 | |||||||
chr16:1563462 | C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+535G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563462 | |||||||
chr16:1563466 | C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+531G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563466 | |||||||
chr16:1563470 | C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+527G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563470 | |||||||
chr16:1563585 | A | G | 1 | a0030c0034t0003g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2067+412T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563585 | |||||||
chr16:1563749 | T | C | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+248A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563749 | |||||||
chr16:1563752 | C | T | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+245G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563752 | |||||||
chr16:1563792 | A | C | 110 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2067+205T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563792 | |||||||
chr16:1563845 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2067+152G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563845 | |||||||
chr16:1563923 | A | G | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+74T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563923 | |||||||
chr16:1563933 | G | C | 4 | a0006c0007t0003g0159 a0006c0007t0003g0161 a0006c0007t0003g0162 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+64C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563933 | |||||||
chr16:1564183 | C | A | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1902-21G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564183 | |||||||
chr16:1564191 | C | T | 1 | a0003c0005t0001g0144 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1902-29G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564191 | |||||||
chr16:1564239 | C | G | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1902-77G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564239 | |||||||
chr16:1564255 | T | C | 4 | a0002c0003t0003g0020 a0002c0003t0003g0026 a0024c0033t0003g0018 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1902-93A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564255 | |||||||
chr16:1564258 | C | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1902-96G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564258 | |||||||
chr16:1564355 | G | C | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1902-193C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564355 | |||||||
chr16:1564366 | C | T | 1 | a0001c0004t0003g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1902-204G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564366 | |||||||
chr16:1564521 | C | T | 3 | a0003c0005t0003g0063 a0011c0012t0003g0201 a0011c0012t0003g0202 |
3 | NA19043.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1902-359G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564521 | |||||||
chr16:1564524 | G | C | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1902-362C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564524 | |||||||
chr16:1564568 | A | C | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-406T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564568 | |||||||
chr16:1564569 | C | A | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-407G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564569 | |||||||
chr16:1564610 | C | A | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1902-448G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564610 | |||||||
chr16:1564688 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1902-526G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564688 | |||||||
chr16:1564725 | G | GT | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1902-564dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564725 | |||||||
chr16:1564754 | C | G | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1902-592G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564754 | |||||||
chr16:1564762 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1902-600C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564762 | |||||||
chr16:1564822 | A | T | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902-660T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564822 | |||||||
chr16:1564860 | C | T | 2 | a0022c0028t0001g0057 a0026c0027t0003g0134 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1902-698G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564860 | |||||||
chr16:1565029 | C | T | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1902-867G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565029 | |||||||
chr16:1565067 | G | A | 2 | a0001c0004t0003g0087 a0001c0004t0003g0100 |
2 | HG00639.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1902-905C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565067 | |||||||
chr16:1565120 | G | T | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-958C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565120 | |||||||
chr16:1565121 | C | G | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-959G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565121 | |||||||
chr16:1565188 | G | A | 26 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(23): Show |
26 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1901+973C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565188 | |||||||
chr16:1565472 | A | G | 6 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1901+689T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565472 | |||||||
chr16:1565489 | G | A | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1901+672C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565489 | |||||||
chr16:1565785 | C | T | 1 | a0019c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1901+376G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565785 | |||||||
chr16:1565827 | C | G | 2 | a0001c0001t0002g0169 a0001c0001t0002g0184 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1901+334G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565827 | |||||||
chr16:1565831 | C | G | 3 | a0001c0002t0001g0113 a0001c0004t0003g0112 a0001c0004t0003g0130 |
3 | NA18945.hp1 NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1901+330G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565831 | |||||||
chr16:1565847 | G | T | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1901+314C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565847 | |||||||
chr16:1566419 | C | T | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1771-128G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566419 | |||||||
chr16:1566527 | T | A | 7 | a0001c0001t0002g0245 a0001c0001t0002g0254 a0001c0001t0002g0261 others(4): Show |
7 | HG01109.hp1 HG01255.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1771-236A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566527 | |||||||
chr16:1566547 | C | T | 1 | a0001c0052t0004g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1771-256G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566547 | |||||||
chr16:1566662 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1771-371G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566662 | |||||||
chr16:1566721 | G | A | 6 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1771-430C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566721 | |||||||
chr16:1566837 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1771-546G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566837 | |||||||
chr16:1566959 | C | T | 3 | a0001c0004t0003g0078 a0001c0004t0003g0087 a0001c0004t0003g0100 |
3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1771-668G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566959 | |||||||
chr16:1567004 | T | G | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1771-713A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567004 | |||||||
chr16:1567016 | C | T | 3 | a0003c0005t0001g0143 a0003c0005t0001g0144 a0003c0005t0001g0145 |
3 | NA18948.hp2 NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1771-725G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567016 | |||||||
chr16:1567075 | C | T | 1 | a0002c0003t0003g0009 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1771-784G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567075 | |||||||
chr16:1567177 | C | G | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1771-886G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567177 | |||||||
chr16:1567240 | G | A | 8 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1771-949C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567240 | |||||||
chr16:1567362 | C | T | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1770+855G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567362 | |||||||
chr16:1567392 | GCCTCTGC | G | 11 | a0001c0008t0001g0203 a0006c0007t0003g0159 a0006c0007t0003g0160 others(8): Show |
11 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1770+818_1770+824d others(9): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567392 | |||||||
chr16:1567430 | C | CACCCGCT others(13): Show |
1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1770+767_1770+786d others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567430 | |||||||
chr16:1567539 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1770+678G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567539 | |||||||
chr16:1567627 | G | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1770+590C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567627 | |||||||
chr16:1567687 | C | G | 85 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0002c0003t0003g0006 others(82): Show |
85 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1770+530G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567687 | |||||||
chr16:1567688 | G | A | 3 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 |
3 | HG02922.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1770+529C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567688 | |||||||
chr16:1567886 | T | C | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1770+331A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567886 | |||||||
chr16:1567994 | G | A | 1 | a0001c0004t0001g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1770+223C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567994 | |||||||
chr16:1568006 | C | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1770+211G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568006 | |||||||
chr16:1568042 | G | A | 7 | a0001c0002t0001g0047 a0001c0002t0001g0082 a0001c0002t0001g0096 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1770+175C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568042 | |||||||
chr16:1568091 | G | A | 1 | a0008c0040t0003g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1770+126C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568091 | |||||||
chr16:1568111 | A | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1770+106T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568111 | |||||||
chr16:1568348 | G | A | 1 | a0001c0001t0002g0278 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1653-14C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568348 | |||||||
chr16:1568361 | G | A | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1653-27C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568361 | |||||||
chr16:1568555 | G | A | 1 | a0001c0004t0003g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1653-221C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568555 | |||||||
chr16:1568704 | A | G | 1 | a0001c0002t0001g0098 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1653-370T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568704 | |||||||
chr16:1568757 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1653-423T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568757 | |||||||
chr16:1568771 | A | C | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1653-437T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568771 | |||||||
chr16:1568835 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653-501G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568835 | |||||||
chr16:1568853 | G | A | 8 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1653-519C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568853 | |||||||
chr16:1568914 | G | C | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1653-580C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568914 | |||||||
chr16:1568994 | T | C | 3 | a0001c0001t0002g0254 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01109.hp1 HG01255.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1653-660A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568994 | |||||||
chr16:1569003 | G | GT | 13 | a0001c0001t0002g0184 a0001c0001t0002g0257 a0001c0001t0002g0267 others(10): Show |
13 | HG00621.hp1 HG01070.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1653-670dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569003 | |||||||
chr16:1569003 | GT | G | 32 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(29): Show |
32 | HG00408.hp1 HG00642.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1653-670delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569003 | |||||||
chr16:1569003 | GTT | G | 11 | a0002c0003t0003g0026 a0006c0007t0003g0159 a0006c0007t0003g0160 others(8): Show |
11 | HG00544.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1653-671_1653-670d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569003 | |||||||
chr16:1569038 | C | T | 11 | a0002c0003t0003g0015 a0006c0007t0003g0159 a0006c0007t0003g0160 others(8): Show |
11 | HG02523.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1653-704G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569038 | |||||||
chr16:1569043 | T | C | 1 | a0002c0003t0003g0015 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1653-709A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569043 | |||||||
chr16:1569043 | T | G | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1653-709A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569043 | |||||||
chr16:1569045 | C | G | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1653-711G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569045 | |||||||
chr16:1569060 | A | G | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1653-726T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569060 | |||||||
chr16:1569065 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0295 |
2 | HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1653-731G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569065 | |||||||
chr16:1569066 | G | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1653-732C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569066 | |||||||
chr16:1569073 | C | T | 89 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0002c0003t0003g0006 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1653-739G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569073 | |||||||
chr16:1569081 | T | C | 90 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0002c0003t0003g0006 others(87): Show |
90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1653-747A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569081 | |||||||
chr16:1569228 | C | T | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1653-894G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569228 | |||||||
chr16:1569251 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1653-917C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569251 | |||||||
chr16:1569255 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1653-921C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569255 | |||||||
chr16:1569260 | A | C | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1653-926T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569260 | |||||||
chr16:1569320 | T | C | 1 | a0001c0002t0001g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1653-986A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569320 | |||||||
chr16:1569363 | C | T | 7 | a0003c0017t0001g0058 a0003c0017t0001g0059 a0010c0015t0003g0053 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1653-1029G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569363 | |||||||
chr16:1569375 | A | G | 2 | a0001c0001t0002g0174 a0005c0009t0004g0167 |
2 | HG01070.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1653-1041T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569375 | |||||||
chr16:1569430 | C | T | 90 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0002c0003t0003g0006 others(87): Show |
90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1653-1096G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569430 | |||||||
chr16:1569487 | C | T | 186 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(183): Show |
186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1653-1153G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569487 | |||||||
chr16:1569675 | T | A | 1 | a0001c0001t0002g0296 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1653-1341A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569675 | |||||||
chr16:1569702 | T | A | 2 | a0001c0002t0001g0120 a0001c0002t0001g0121 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1653-1368A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569702 | |||||||
chr16:1569740 | G | C | 1 | a0007c0013t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1653-1406C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569740 | |||||||
chr16:1569757 | A | AT | 45 | a0001c0020t0003g0138 a0003c0005t0001g0141 a0003c0005t0001g0142 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1653-1424dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569757 | |||||||
chr16:1569757 | A | ATT | 41 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1653-1425_1653-142 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569757 | |||||||
chr16:1569788 | A | T | 2 | a0001c0001t0002g0169 a0001c0001t0002g0184 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1653-1454T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569788 | |||||||
chr16:1569824 | G | C | 4 | a0001c0002t0001g0069 a0001c0002t0001g0197 a0001c0002t0010g0186 others(1): Show |
4 | HG00621.hp2 NA18962.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653-1490C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569824 | |||||||
chr16:1569895 | A | T | 48 | a0001c0001t0002g0298 a0001c0020t0003g0138 a0001c0020t0003g0139 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1652+1512T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569895 | |||||||
chr16:1569961 | T | C | 1 | a0001c0001t0002g0332 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1652+1446A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569961 | |||||||
chr16:1570025 | G | T | 1 | a0001c0004t0001g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1652+1382C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570025 | |||||||
chr16:1570306 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1652+1101G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570306 | |||||||
chr16:1570383 | C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1652+1024G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570383 | |||||||
chr16:1570467 | G | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1652+940C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570467 | |||||||
chr16:1570517 | C | T | 1 | a0016c0038t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1652+890G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570517 | |||||||
chr16:1570520 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1652+887T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570520 | |||||||
chr16:1570549 | C | T | 31 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(28): Show |
31 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1652+858G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570549 | |||||||
chr16:1570818 | C | T | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1652+589G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570818 | |||||||
chr16:1570889 | G | A | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1652+518C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570889 | |||||||
chr16:1570924 | T | G | 1 | a0001c0002t0001g0088 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1652+483A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570924 | |||||||
chr16:1570948 | G | C | 1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1652+459C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570948 | |||||||
chr16:1571011 | C | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1652+396G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571011 | |||||||
chr16:1571097 | CTT | C | 4 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1652+308_1652+309d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571097 | |||||||
chr16:1571118 | G | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1652+289C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571118 | |||||||
chr16:1571152 | C | G | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1652+255G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571152 | |||||||
chr16:1571157 | A | G | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1652+250T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571157 | |||||||
chr16:1571332 | T | C | 1 | a0001c0010t0004g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1652+75A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571332 | |||||||
chr16:1571701 | C | T | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1525-167G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571701 | |||||||
chr16:1571719 | G | A | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-185C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571719 | |||||||
chr16:1571748 | G | C | 1 | a0001c0002t0001g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1525-214C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571748 | |||||||
chr16:1571927 | G | A | 2 | a0002c0003t0003g0007 a0002c0003t0003g0009 |
2 | NA18941.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1525-393C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571927 | |||||||
chr16:1571966 | T | C | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1525-432A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571966 | |||||||
chr16:1572007 | A | G | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-473T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572007 | |||||||
chr16:1572036 | G | A | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-502C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572036 | |||||||
chr16:1572091 | C | T | 80 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1525-557G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572091 | |||||||
chr16:1572107 | G | A | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-573C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572107 | |||||||
chr16:1572110 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1525-576C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572110 | |||||||
chr16:1572246 | C | T | 2 | a0001c0001t0002g0205 a0001c0001t0002g0235 |
2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1525-712G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572246 | |||||||
chr16:1572259 | T | C | 4 | a0002c0003t0003g0020 a0002c0003t0003g0026 a0024c0033t0003g0018 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-725A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572259 | |||||||
chr16:1572273 | G | A | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1525-739C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572273 | |||||||
chr16:1572372 | C | A | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1525-838G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572372 | |||||||
chr16:1572538 | C | T | 2 | a0001c0001t0002g0288 a0001c0001t0002g0289 |
2 | HG01099.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1525-1004G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572538 | |||||||
chr16:1572725 | G | T | 1 | a0001c0002t0003g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1525-1191C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572725 | |||||||
chr16:1572900 | C | G | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-1366G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572900 | |||||||
chr16:1572900 | C | T | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1525-1366G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572900 | |||||||
chr16:1572917 | C | G | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1525-1383G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572917 | |||||||
chr16:1573250 | G | A | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-1716C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573250 | |||||||
chr16:1573358 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1525-1824G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573358 | |||||||
chr16:1573472 | CTTGTATT | C | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-1945_1525-193 others(11): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573472 | |||||||
chr16:1573630 | G | C | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1525-2096C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573630 | |||||||
chr16:1573637 | C | T | 5 | a0001c0001t0002g0228 a0001c0001t0002g0253 a0001c0001t0002g0301 others(2): Show |
5 | HG02257.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-2103G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573637 | |||||||
chr16:1573745 | A | AGGCT | 5 | a0001c0008t0001g0203 a0001c0008t0001g0211 a0001c0008t0001g0216 others(2): Show |
5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-2215_1525-221 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573745 | |||||||
chr16:1573851 | A | G | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-2317T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573851 | |||||||
chr16:1573879 | T | C | 8 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525-2345A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573879 | |||||||
chr16:1573911 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-2377C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573911 | |||||||
chr16:1573935 | C | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-2401G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573935 | |||||||
chr16:1573990 | T | C | 2 | a0001c0004t0001g0074 a0001c0004t0001g0075 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1525-2456A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573990 | |||||||
chr16:1574141 | T | C | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-2607A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574141 | |||||||
chr16:1574476 | T | C | 1 | a0001c0002t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1525-2942A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574476 | |||||||
chr16:1574492 | G | A | 80 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1525-2958C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574492 | |||||||
chr16:1574527 | C | T | 34 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1525-2993G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574527 | |||||||
chr16:1574770 | CCCCT | C | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-3240_1525-323 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574770 | |||||||
chr16:1574783 | T | G | 115 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1525-3249A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574783 | |||||||
chr16:1574942 | T | C | 1 | a0001c0004t0001g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1525-3408A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574942 | |||||||
chr16:1575142 | G | A | 14 | a0001c0002t0001g0047 a0001c0002t0001g0049 a0001c0002t0001g0068 others(11): Show |
14 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1525-3608C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575142 | |||||||
chr16:1575184 | A | T | 1 | a0001c0001t0002g0257 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1525-3650T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575184 | |||||||
chr16:1575243 | T | G | 116 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(113): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1525-3709A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575243 | |||||||
chr16:1575289 | G | A | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-3755C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575289 | |||||||
chr16:1575299 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1525-3765G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575299 | |||||||
chr16:1575345 | A | T | 1 | a0001c0010t0002g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1525-3811T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575345 | |||||||
chr16:1575350 | G | C | 1 | a0001c0010t0002g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1525-3816C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575350 | |||||||
chr16:1575445 | C | T | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1525-3911G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575445 | |||||||
chr16:1575812 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1525-4278G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575812 | |||||||
chr16:1575889 | T | C | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-4355A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575889 | |||||||
chr16:1575936 | G | C | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-4402C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575936 | |||||||
chr16:1575960 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1525-4426C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575960 | |||||||
chr16:1576057 | G | A | 34 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1525-4523C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576057 | |||||||
chr16:1576072 | G | C | 1 | a0001c0054t0001g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1525-4538C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576072 | |||||||
chr16:1576078 | A | G | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-4544T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576078 | |||||||
chr16:1576286 | T | TA | 83 | a0001c0001t0002g0179 a0001c0001t0002g0299 a0001c0001t0002g0319 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1524+4472dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576286 | |||||||
chr16:1576286 | TA | T | 21 | a0001c0001t0002g0205 a0001c0001t0002g0232 a0001c0001t0002g0285 others(18): Show |
21 | HG01256.hp2 HG01433.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1524+4472delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576286 | |||||||
chr16:1576287 | A | T | 1 | a0001c0001t0002g0321 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1524+4472T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576287 | |||||||
chr16:1576317 | T | C | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+4442A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576317 | |||||||
chr16:1576358 | G | A | 1 | a0001c0002t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1524+4401C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576358 | |||||||
chr16:1576363 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1524+4396C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576363 | |||||||
chr16:1576465 | G | A | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+4294C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576465 | |||||||
chr16:1576490 | G | A | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+4269C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576490 | |||||||
chr16:1576523 | C | T | 1 | a0001c0004t0003g0014 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1524+4236G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576523 | |||||||
chr16:1576547 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1524+4212C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576547 | |||||||
chr16:1576591 | C | CA | 128 | a0001c0001t0002g0169 a0001c0001t0002g0179 a0001c0001t0002g0184 others(125): Show |
128 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1524+4167dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576591 | |||||||
chr16:1576605 | AC | A | 4 | a0003c0005t0001g0147 a0006c0007t0003g0161 a0011c0012t0003g0051 others(1): Show |
4 | HG02897.hp2 HG03017.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+4153delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576605 | |||||||
chr16:1576606 | C | A | 82 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1524+4153G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576606 | |||||||
chr16:1576651 | TCAGA | T | 77 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0047 others(74): Show |
77 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1524+4104_1524+410 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576651 | |||||||
chr16:1576704 | T | A | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+4055A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576704 | |||||||
chr16:1576831 | C | T | 3 | a0001c0002t0001g0086 a0001c0002t0001g0088 a0001c0002t0001g0091 |
3 | HG00423.hp1 NA18980.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1524+3928G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576831 | |||||||
chr16:1576888 | C | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1524+3871G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576888 | |||||||
chr16:1576981 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1524+3778C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576981 | |||||||
chr16:1577437 | G | A | 2 | a0001c0002t0001g0041 a0001c0054t0001g0119 |
2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1524+3322C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577437 | |||||||
chr16:1577507 | A | G | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+3252T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577507 | |||||||
chr16:1577617 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1524+3142C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577617 | |||||||
chr16:1577724 | G | C | 1 | a0001c0001t0004g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1524+3035C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577724 | |||||||
chr16:1577754 | C | T | 86 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+3005G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577754 | |||||||
chr16:1577972 | C | CAA | 88 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(85): Show |
88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1524+2785_1524+278 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577972 | |||||||
chr16:1577994 | G | C | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2765C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577994 | |||||||
chr16:1577997 | A | G | 7 | a0002c0003t0003g0011 a0002c0003t0003g0016 a0002c0003t0003g0021 others(4): Show |
7 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+2762T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577997 | |||||||
chr16:1578078 | C | T | 2 | a0011c0012t0003g0201 a0011c0012t0003g0202 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1524+2681G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578078 | |||||||
chr16:1578130 | C | T | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2629G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578130 | |||||||
chr16:1578176 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1524+2583A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578176 | |||||||
chr16:1578224 | T | G | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1524+2535A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578224 | |||||||
chr16:1578294 | G | A | 36 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1524+2465C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578294 | |||||||
chr16:1578333 | C | T | 1 | a0005c0009t0004g0173 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1524+2426G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578333 | |||||||
chr16:1578578 | TA | T | 151 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(148): Show |
151 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1524+2180delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578578 | |||||||
chr16:1578603 | C | T | 1 | a0001c0004t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1524+2156G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578603 | |||||||
chr16:1578857 | G | A | 3 | a0003c0019t0003g0136 a0003c0019t0003g0137 a0026c0027t0003g0134 |
3 | HG02896.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1524+1902C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578857 | |||||||
chr16:1578878 | A | AT | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+1880dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578878 | |||||||
chr16:1578964 | G | A | 2 | a0001c0004t0001g0074 a0001c0004t0001g0075 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1524+1795C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578964 | |||||||
chr16:1579060 | T | C | 1 | a0001c0002t0010g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1524+1699A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579060 | |||||||
chr16:1579191 | G | T | 1 | a0001c0001t0002g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1524+1568C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579191 | |||||||
chr16:1579257 | C | T | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+1502G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579257 | |||||||
chr16:1579280 | G | A | 1 | a0001c0004t0003g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1524+1479C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579280 | |||||||
chr16:1579297 | G | T | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1524+1462C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579297 | |||||||
chr16:1579624 | AGT | A | 3 | a0001c0004t0003g0078 a0001c0004t0003g0087 a0001c0004t0003g0100 |
3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1524+1133_1524+113 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579624 | |||||||
chr16:1579748 | C | G | 1 | a0005c0049t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1524+1011G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579748 | |||||||
chr16:1579773 | T | G | 1 | a0001c0001t0002g0324 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1524+986A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579773 | |||||||
chr16:1579963 | C | CA | 49 | a0001c0001t0002g0239 a0001c0001t0002g0266 a0001c0001t0002g0267 others(46): Show |
49 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1524+795dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579963 | |||||||
chr16:1579963 | CA | C | 37 | a0001c0001t0002g0245 a0001c0002t0001g0212 a0003c0005t0001g0141 others(34): Show |
37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1524+795delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579963 | |||||||
chr16:1580129 | C | T | 1 | a0008c0021t0002g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1524+630G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580129 | |||||||
chr16:1580184 | T | C | 52 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(49): Show |
52 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1524+575A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580184 | |||||||
chr16:1580262 | G | A | 6 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+497C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580262 | |||||||
chr16:1580263 | C | T | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1524+496G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580263 | |||||||
chr16:1580287 | A | G | 1 | a0001c0002t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1524+472T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580287 | |||||||
chr16:1580323 | G | A | 1 | a0001c0010t0004g0238 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1524+436C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580323 | |||||||
chr16:1580347 | G | C | 1 | a0002c0003t0003g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1524+412C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580347 | |||||||
chr16:1580380 | G | A | 116 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(113): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1524+379C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580380 | |||||||
chr16:1580452 | G | T | 2 | a0013c0023t0001g0048 a0013c0023t0001g0060 |
2 | NA18948.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1524+307C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580452 | |||||||
chr16:1580554 | G | A | 1 | a0001c0004t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1524+205C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580554 | |||||||
chr16:1580745 | G | C | 1 | a0001c0004t0003g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1524+14C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580745 | |||||||
chr16:1580885 | C | A | 3 | a0001c0002t0001g0103 a0001c0002t0001g0333 a0001c0002t0001g0334 |
3 | HG02896.hp1 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1433-35G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1580885 | |||||||
chr16:1580988 | C | T | 5 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1433-138G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1580988 | |||||||
chr16:1581013 | A | G | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1433-163T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581013 | |||||||
chr16:1581231 | T | C | 1 | a0003c0005t0003g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1433-381A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581231 | |||||||
chr16:1581238 | A | C | 1 | a0001c0001t0002g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1433-388T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581238 | |||||||
chr16:1581281 | A | C | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1433-431T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581281 | |||||||
chr16:1581293 | A | G | 8 | a0001c0001t0002g0245 a0001c0001t0002g0254 a0001c0001t0002g0261 others(5): Show |
8 | HG01109.hp1 HG01255.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1433-443T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581293 | |||||||
chr16:1581514 | C | T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0175 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1433-664G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581514 | |||||||
chr16:1581521 | G | A | 1 | a0010c0015t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1433-671C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581521 | |||||||
chr16:1581535 | G | A | 31 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(28): Show |
31 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1433-685C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581535 | |||||||
chr16:1581590 | A | ACT | 91 | a0001c0001t0003g0038 a0001c0020t0003g0138 a0001c0020t0003g0139 others(88): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1433-742_1433-741d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581590 | |||||||
chr16:1581653 | A | C | 1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1433-803T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581653 | |||||||
chr16:1581727 | A | AGGGGAGG others(4): Show |
1 | a0001c0001t0003g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1433-888_1433-878d others(13): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581727 | |||||||
chr16:1581738 | GGGGGAGG others(17): Show |
G | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1433-912_1433-889d others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581738 | |||||||
chr16:1581755 | C | CG | 13 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0330 others(10): Show |
13 | HG01123.hp2 HG01175.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1433-906dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581755 | |||||||
chr16:1581755 | C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1433-905G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581755 | |||||||
chr16:1581758 | G | T | 1 | a0001c0001t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1433-908C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581758 | |||||||
chr16:1581761 | G | A | 32 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1433-911C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581761 | |||||||
chr16:1581784 | G | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1433-934C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581784 | |||||||
chr16:1581808 | T | G | 91 | a0001c0001t0003g0038 a0001c0020t0003g0138 a0001c0020t0003g0139 others(88): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1433-958A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581808 | |||||||
chr16:1581814 | T | G | 10 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(7): Show |
10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1433-964A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581814 | |||||||
chr16:1581849 | G | A | 11 | a0001c0002t0001g0049 a0006c0007t0003g0159 a0006c0007t0003g0160 others(8): Show |
11 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1433-999C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581849 | |||||||
chr16:1581881 | A | G | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1433-1031T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581881 | |||||||
chr16:1581998 | C | T | 2 | a0001c0002t0005g0001 a0001c0002t0005g0002 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1433-1148G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581998 | |||||||
chr16:1582085 | C | A | 1 | a0001c0001t0004g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1432+1229G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582085 | |||||||
chr16:1582124 | G | A | 2 | a0001c0045t0002g0176 a0005c0044t0004g0168 |
2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1432+1190C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582124 | |||||||
chr16:1582270 | C | T | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+1044G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582270 | |||||||
chr16:1582447 | C | T | 30 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(27): Show |
30 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1432+867G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582447 | |||||||
chr16:1582688 | G | A | 2 | a0001c0004t0003g0014 a0014c0042t0001g0108 |
2 | HG00673.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1432+626C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582688 | |||||||
chr16:1582693 | C | G | 5 | a0001c0008t0001g0203 a0001c0008t0001g0211 a0001c0008t0001g0216 others(2): Show |
5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+621G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582693 | |||||||
chr16:1582699 | T | C | 1 | a0001c0002t0003g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1432+615A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582699 | |||||||
chr16:1582900 | C | T | 5 | a0001c0001t0002g0228 a0001c0001t0002g0253 a0001c0001t0002g0301 others(2): Show |
5 | HG02257.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+414G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582900 | |||||||
chr16:1582904 | G | A | 2 | a0001c0014t0006g0209 a0001c0014t0006g0215 |
2 | HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1432+410C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582904 | |||||||
chr16:1582964 | G | A | 90 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0002c0003t0003g0006 others(87): Show |
90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1432+350C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582964 | |||||||
chr16:1583099 | A | G | 44 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1432+215T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1583099 | |||||||
chr16:1583136 | T | G | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1432+178A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1583136 | |||||||
chr16:1583421 | G | A | 1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1360-35C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583421 | |||||||
chr16:1583445 | A | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0295 |
2 | HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1360-59T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583445 | |||||||
chr16:1583557 | C | T | 3 | a0001c0002t0001g0210 a0001c0002t0001g0220 a0001c0043t0001g0219 |
3 | HG02071.hp1 HG02129.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1360-171G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583557 | |||||||
chr16:1583664 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1360-278A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583664 | |||||||
chr16:1583757 | T | G | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1360-371A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583757 | |||||||
chr16:1583784 | G | A | 1 | a0005c0009t0004g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1360-398C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583784 | |||||||
chr16:1583849 | A | G | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1359+368T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583849 | |||||||
chr16:1583854 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1359+363G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583854 | |||||||
chr16:1583871 | G | A | 91 | a0001c0001t0003g0038 a0001c0020t0003g0138 a0001c0020t0003g0139 others(88): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1359+346C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583871 | |||||||
chr16:1583890 | A | G | 5 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0175 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359+327T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583890 | |||||||
chr16:1583945 | G | C | 43 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1359+272C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583945 | |||||||
chr16:1583978 | G | C | 3 | a0003c0019t0003g0136 a0003c0019t0003g0137 a0026c0027t0003g0134 |
3 | HG02896.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1359+239C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583978 | |||||||
chr16:1584505 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1156-85C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584505 | |||||||
chr16:1584556 | T | C | 1 | a0001c0010t0004g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1156-136A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584556 | |||||||
chr16:1584603 | T | A | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156-183A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584603 | |||||||
chr16:1584837 | A | G | 1 | a0001c0001t0002g0310 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1156-417T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584837 | |||||||
chr16:1585136 | G | A | 58 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0061 others(55): Show |
58 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1156-716C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585136 | |||||||
chr16:1585160 | A | G | 11 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0146 others(8): Show |
11 | HG00099.hp2 HG01192.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156-740T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585160 | |||||||
chr16:1585375 | A | T | 1 | a0001c0002t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1155+755T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585375 | |||||||
chr16:1585399 | TGCCAAGG others(8): Show |
T | 1 | a0006c0007t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1155+716_1155+730d others(17): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585399 | |||||||
chr16:1585751 | T | C | 43 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1155+379A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585751 | |||||||
chr16:1585766 | C | CT | 30 | a0001c0001t0002g0184 a0001c0001t0002g0232 a0001c0001t0002g0248 others(27): Show |
30 | HG00673.hp2 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1155+363dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585766 | |||||||
chr16:1585766 | CT | C | 11 | a0001c0001t0002g0245 a0001c0001t0002g0317 a0001c0001t0002g0320 others(8): Show |
11 | HG00099.hp2 HG01070.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155+363delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585766 | |||||||
chr16:1585775 | T | C | 1 | a0001c0001t0002g0325 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1155+355A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585775 | |||||||
chr16:1585822 | G | A | 1 | a0001c0002t0001g0220 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1155+308C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585822 | |||||||
chr16:1585871 | C | T | 33 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(30): Show |
33 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1155+259G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585871 | |||||||
chr16:1585916 | G | T | 1 | a0001c0002t0001g0091 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1155+214C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585916 | |||||||
chr16:1585993 | G | A | 1 | a0002c0003t0003g0021 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1155+137C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585993 | |||||||
chr16:1586027 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | NA18975.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1155+103A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1586027 | |||||||
chr16:1586034 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1155+96C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1586034 | |||||||
chr16:1586073 | G | T | 1 | a0002c0003t0003g0008 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1155+57C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1586073 | |||||||
chr16:1586404 | C | A | 1 | a0001c0010t0002g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1010-129G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586404 | |||||||
chr16:1586548 | C | A | 43 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1010-273G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586548 | |||||||
chr16:1586557 | C | T | 1 | a0001c0001t0002g0318 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1010-282G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586557 | |||||||
chr16:1586627 | G | GCA | 5 | a0001c0001t0002g0174 a0001c0001t0002g0301 a0001c0004t0003g0078 others(2): Show |
5 | HG02257.hp1 HG03453.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-354_1010-353d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586627 | |||||||
chr16:1586627 | GCA | G | 165 | a0001c0001t0003g0038 a0001c0002t0001g0005 a0001c0002t0001g0013 others(162): Show |
165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1010-354_1010-353d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586627 | |||||||
chr16:1586629 | A | G | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1010-354T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586629 | |||||||
chr16:1586718 | T | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1010-443A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586718 | |||||||
chr16:1586826 | C | A | 8 | a0003c0017t0001g0058 a0003c0017t0001g0059 a0003c0059t0001g0050 others(5): Show |
8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009+372G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586826 | |||||||
chr16:1586829 | C | G | 1 | a0001c0001t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1009+369G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586829 | |||||||
chr16:1586895 | C | T | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1009+303G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586895 | |||||||
chr16:1586907 | A | G | 43 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1009+291T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586907 | |||||||
chr16:1586934 | T | G | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1009+264A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586934 | |||||||
chr16:1587140 | C | T | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009+58G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1587140 | |||||||
chr16:1587180 | C | G | 1 | a0001c0001t0002g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1009+18G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1587180 | |||||||
chr16:1587464 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.903-160A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587464 | |||||||
chr16:1587521 | T | C | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.903-217A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587521 | |||||||
chr16:1587705 | G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.902+228C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587705 | |||||||
chr16:1587740 | G | A | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.902+193C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587740 | |||||||
chr16:1587797 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.902+136A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587797 | |||||||
chr16:1588070 | G | A | 1 | a0005c0009t0004g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.811-46C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588070 | |||||||
chr16:1588159 | T | C | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.811-135A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588159 | |||||||
chr16:1588322 | A | G | 38 | a0001c0001t0002g0255 a0001c0001t0003g0038 a0002c0003t0003g0006 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.811-298T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588322 | |||||||
chr16:1588527 | A | AAATAATA others(5): Show |
16 | a0001c0002t0003g0090 a0001c0004t0001g0117 a0001c0020t0003g0138 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.811-515_811-504dup others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | |||||||
chr16:1588527 | A | AAATAATA others(8): Show |
10 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(7): Show |
10 | HG00408.hp1 HG00621.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.811-518_811-504dup others(15): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | |||||||
chr16:1588527 | A | AAATAATA others(11): Show |
116 | a0001c0001t0002g0169 a0001c0001t0002g0184 a0001c0001t0002g0200 others(113): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.811-521_811-504dup others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | |||||||
chr16:1588527 | A | AAATAATA others(14): Show |
57 | a0001c0001t0003g0038 a0001c0001t0004g0170 a0001c0001t0004g0172 others(54): Show |
57 | HG00544.hp1 HG00544.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.811-524_811-504dup others(21): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | |||||||
chr16:1588527 | A | AAATAATA others(17): Show |
10 | a0002c0003t0003g0006 a0002c0003t0003g0023 a0002c0003t0003g0039 others(7): Show |
10 | HG00099.hp2 HG01109.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.811-504_811-503ins others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | |||||||
chr16:1588527 | A | AAATAATA others(20): Show |
3 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0156 |
3 | HG03491.hp2 HG03492.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.811-504_811-503ins others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | |||||||
chr16:1588614 | T | TA | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-591_811-590ins others(1): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588614 | |||||||
chr16:1588615 | C | G | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-591G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588615 | |||||||
chr16:1588735 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.811-711C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588735 | |||||||
chr16:1588819 | C | T | 31 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(28): Show |
31 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.810+786G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588819 | |||||||
chr16:1588846 | A | C | 1 | a0001c0001t0003g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.810+759T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588846 | |||||||
chr16:1588988 | T | C | 54 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(51): Show |
54 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.810+617A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588988 | |||||||
chr16:1589102 | G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.810+503C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589102 | |||||||
chr16:1589127 | G | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.810+478C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589127 | |||||||
chr16:1589217 | T | C | 1 | a0003c0005t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.810+388A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589217 | |||||||
chr16:1589277 | G | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.810+328C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589277 | |||||||
chr16:1589792 | C | G | 91 | a0001c0001t0003g0038 a0001c0004t0003g0115 a0001c0020t0003g0138 others(88): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.635-12G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589792 | |||||||
chr16:1589807 | T | C | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.635-27A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589807 | |||||||
chr16:1589836 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.635-56C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589836 | |||||||
chr16:1589844 | C | G | 1 | a0001c0001t0004g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.635-64G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589844 | |||||||
chr16:1589940 | T | C | 1 | a0001c0004t0003g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.635-160A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589940 | |||||||
chr16:1589963 | G | A | 8 | a0003c0017t0001g0058 a0003c0017t0001g0059 a0003c0059t0001g0050 others(5): Show |
8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-183C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589963 | |||||||
chr16:1590034 | T | C | 31 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(28): Show |
31 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.635-254A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590034 | |||||||
chr16:1590062 | G | A | 1 | a0001c0001t0002g0331 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.635-282C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590062 | |||||||
chr16:1590200 | C | CA | 108 | a0001c0001t0002g0267 a0001c0001t0002g0269 a0001c0001t0002g0280 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.635-421dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | |||||||
chr16:1590200 | C | CAA | 13 | a0001c0002t0001g0064 a0001c0002t0001g0069 a0001c0002t0001g0079 others(10): Show |
13 | HG00621.hp2 HG02040.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.635-422_635-421dup others(2): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | |||||||
chr16:1590200 | CA | C | 17 | a0001c0001t0002g0309 a0001c0001t0002g0318 a0001c0020t0003g0138 others(14): Show |
17 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.635-421delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | |||||||
chr16:1590200 | CAA | C | 31 | a0003c0005t0001g0141 a0003c0005t0001g0143 a0003c0005t0001g0144 others(28): Show |
31 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.635-422_635-421del others(2): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | |||||||
chr16:1590248 | C | G | 1 | a0001c0004t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.635-468G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590248 | |||||||
chr16:1590300 | C | G | 37 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(34): Show |
37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.635-520G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590300 | |||||||
chr16:1590332 | G | A | 2 | a0001c0020t0003g0138 a0001c0020t0003g0139 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.635-552C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590332 | |||||||
chr16:1590438 | G | A | 5 | a0001c0008t0001g0203 a0001c0008t0001g0211 a0001c0008t0001g0216 others(2): Show |
5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-658C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590438 | |||||||
chr16:1590614 | C | T | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.635-834G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590614 | |||||||
chr16:1590712 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.635-932G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590712 | |||||||
chr16:1590994 | A | G | 2 | a0001c0002t0001g0041 a0001c0054t0001g0119 |
2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.634+1182T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590994 | |||||||
chr16:1591008 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.634+1168G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591008 | |||||||
chr16:1591071 | T | C | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.634+1105A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591071 | |||||||
chr16:1591092 | C | T | 5 | a0002c0003t0003g0035 a0009c0011t0003g0042 a0009c0011t0003g0043 others(2): Show |
5 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+1084G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591092 | |||||||
chr16:1591117 | T | C | 4 | a0001c0002t0001g0064 a0001c0002t0001g0085 a0001c0002t0001g0101 others(1): Show |
4 | HG02040.hp1 HG02155.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+1059A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591117 | |||||||
chr16:1591210 | C | T | 1 | a0004c0006t0002g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.634+966G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591210 | |||||||
chr16:1591281 | C | T | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+895G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591281 | |||||||
chr16:1591354 | T | C | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.634+822A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591354 | |||||||
chr16:1591550 | C | T | 32 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.634+626G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591550 | |||||||
chr16:1591571 | G | A | 2 | a0001c0020t0003g0138 a0001c0020t0003g0139 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.634+605C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591571 | |||||||
chr16:1591713 | A | T | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.634+463T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591713 | |||||||
chr16:1591770 | T | C | 3 | a0003c0019t0003g0136 a0003c0019t0003g0137 a0026c0027t0003g0134 |
3 | HG02896.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.634+406A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591770 | |||||||
chr16:1591977 | C | T | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+199G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591977 | |||||||
chr16:1591982 | G | A | 1 | a0001c0004t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.634+194C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591982 | |||||||
chr16:1591994 | C | T | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.634+182G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591994 | |||||||
chr16:1592025 | G | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0295 |
2 | HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.634+151C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1592025 | |||||||
chr16:1592073 | A | G | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.634+103T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1592073 | |||||||
chr16:1592332 | C | T | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.492-14G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592332 | |||||||
chr16:1592338 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.492-20C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592338 | |||||||
chr16:1592422 | C | T | 92 | a0001c0001t0003g0038 a0001c0020t0003g0138 a0001c0020t0003g0139 others(89): Show |
92 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.491+45G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592422 | |||||||
chr16:1592460 | C | T | 4 | a0001c0001t0002g0290 a0001c0001t0002g0296 a0001c0001t0002g0297 others(1): Show |
4 | NA18962.hp2 NA18991.hp2 NA19081.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.491+7G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592460 | |||||||
chr16:1592614 | A | AGGACAGG others(25): Show |
17 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(14): Show |
17 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.370-58_370-27dupCT others(30): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592614 | |||||||
chr16:1592614 | AGGACAGG others(57): Show |
A | 38 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(35): Show |
38 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.370-90_370-27delCA others(62): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592614 | |||||||
chr16:1592635 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.370-47G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592635 | |||||||
chr16:1592659 | T | C | 54 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(51): Show |
54 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-71A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592659 | |||||||
chr16:1592755 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.370-167G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592755 | |||||||
chr16:1592845 | G | A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0118 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.370-257C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592845 | |||||||
chr16:1592892 | A | AGGACAGG others(153): Show |
2 | a0001c0002t0005g0001 a0001c0002t0005g0002 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.370-464_370-305dup others(160): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592892 | |||||||
chr16:1592905 | T | C | 40 | a0001c0001t0002g0182 a0001c0001t0002g0244 a0001c0001t0003g0038 others(37): Show |
40 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-317A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592905 | |||||||
chr16:1592969 | C | CGGCAGAG others(25): Show |
11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.370-413_370-382dup others(32): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592969 | |||||||
chr16:1593246 | C | T | 9 | a0004c0006t0002g0204 a0004c0006t0002g0241 a0004c0006t0002g0243 others(6): Show |
9 | HG00733.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-658G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593246 | |||||||
chr16:1593315 | CT | C | 8 | a0001c0001t0002g0259 a0001c0002t0001g0047 a0001c0002t0001g0082 others(5): Show |
8 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-728delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593315 | |||||||
chr16:1593397 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-809G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593397 | |||||||
chr16:1593551 | C | T | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.370-963G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593551 | |||||||
chr16:1593605 | A | T | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.370-1017T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593605 | |||||||
chr16:1593635 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-1047C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593635 | |||||||
chr16:1593636 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-1048C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593636 | |||||||
chr16:1593675 | G | A | 1 | a0002c0003t0003g0040 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.370-1087C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593675 | |||||||
chr16:1593819 | T | C | 1 | a0019c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.370-1231A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593819 | |||||||
chr16:1593855 | G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.370-1267C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593855 | |||||||
chr16:1593949 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.370-1361G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593949 | |||||||
chr16:1594031 | C | T | 2 | a0001c0001t0007g0265 a0001c0001t0007g0270 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.370-1443G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594031 | |||||||
chr16:1594178 | T | C | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.370-1590A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594178 | |||||||
chr16:1594221 | T | G | 1 | a0025c0024t0001g0111 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.370-1633A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594221 | |||||||
chr16:1594226 | G | GT | 41 | a0001c0001t0002g0205 a0001c0001t0002g0230 a0001c0001t0002g0234 others(38): Show |
41 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.370-1639dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594226 | |||||||
chr16:1594311 | C | G | 49 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.370-1723G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594311 | |||||||
chr16:1594368 | T | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-1780A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594368 | |||||||
chr16:1594477 | T | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.370-1889A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594477 | |||||||
chr16:1594596 | G | A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0118 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.370-2008C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594596 | |||||||
chr16:1594656 | G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.370-2068C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594656 | |||||||
chr16:1594710 | C | G | 2 | a0001c0001t0002g0293 a0001c0001t0002g0294 |
2 | NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.370-2122G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594710 | |||||||
chr16:1594763 | A | G | 55 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(52): Show |
55 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.370-2175T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594763 | |||||||
chr16:1594807 | C | G | 40 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-2219G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594807 | |||||||
chr16:1594847 | C | A | 1 | a0007c0013t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.370-2259G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594847 | |||||||
chr16:1594870 | C | T | 1 | a0007c0013t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.370-2282G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594870 | |||||||
chr16:1594898 | T | C | 12 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0001c0001t0002g0318 others(9): Show |
12 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-2310A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594898 | |||||||
chr16:1594917 | C | CAATCTCC others(3): Show |
1 | a0001c0001t0002g0259 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.370-2339_370-2330d others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594917 | |||||||
chr16:1595056 | C | T | 4 | a0001c0001t0002g0317 a0001c0001t0002g0320 a0008c0021t0002g0315 others(1): Show |
4 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-2468G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595056 | |||||||
chr16:1595057 | G | A | 39 | a0001c0002t0001g0064 a0001c0020t0003g0138 a0001c0020t0003g0139 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.370-2469C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595057 | |||||||
chr16:1595059 | G | T | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.370-2471C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595059 | |||||||
chr16:1595079 | A | G | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.370-2491T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595079 | |||||||
chr16:1595242 | G | C | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-2654C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595242 | |||||||
chr16:1595263 | T | C | 199 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(196): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.370-2675A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595263 | |||||||
chr16:1595603 | G | GA | 56 | a0001c0001t0003g0038 a0001c0002t0001g0064 a0001c0002t0001g0085 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.370-3016dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595603 | |||||||
chr16:1595658 | G | T | 1 | a0002c0003t0003g0022 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.370-3070C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595658 | |||||||
chr16:1595691 | A | G | 2 | a0001c0002t0001g0080 a0001c0004t0003g0081 |
2 | NA18961.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.370-3103T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595691 | |||||||
chr16:1595744 | T | C | 38 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(35): Show |
38 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.370-3156A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595744 | |||||||
chr16:1595818 | C | T | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.370-3230G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595818 | |||||||
chr16:1595824 | G | T | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-3236C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595824 | |||||||
chr16:1595826 | A | G | 199 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(196): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.370-3238T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595826 | |||||||
chr16:1595874 | G | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.370-3286C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595874 | |||||||
chr16:1596010 | C | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.370-3422G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596010 | |||||||
chr16:1596012 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.370-3424G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596012 | |||||||
chr16:1596017 | C | T | 107 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.370-3429G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596017 | |||||||
chr16:1596050 | C | T | 7 | a0001c0002t0001g0047 a0001c0002t0001g0082 a0001c0002t0001g0096 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-3462G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596050 | |||||||
chr16:1596193 | C | G | 3 | a0001c0010t0004g0225 a0001c0010t0004g0238 a0001c0052t0004g0242 |
3 | HG02132.hp2 HG02135.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.370-3605G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596193 | |||||||
chr16:1596426 | A | C | 1 | a0001c0004t0003g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.370-3838T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596426 | |||||||
chr16:1596486 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.370-3898G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596486 | |||||||
chr16:1596517 | G | A | 1 | a0016c0038t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.370-3929C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596517 | |||||||
chr16:1596542 | G | A | 55 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(52): Show |
55 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.370-3954C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596542 | |||||||
chr16:1596578 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.370-3990C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596578 | |||||||
chr16:1596655 | C | T | 9 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(6): Show |
9 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-4067G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596655 | |||||||
chr16:1596874 | AG | A | 8 | a0003c0017t0001g0058 a0003c0017t0001g0059 a0003c0059t0001g0050 others(5): Show |
8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-4287delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596874 | |||||||
chr16:1596878 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-4290C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596878 | |||||||
chr16:1596933 | A | C | 30 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(27): Show |
30 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.370-4345T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596933 | |||||||
chr16:1596942 | G | A | 7 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(4): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-4354C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596942 | |||||||
chr16:1596972 | C | A | 1 | a0001c0001t0002g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.370-4384G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596972 | |||||||
chr16:1597056 | T | C | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.370-4468A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597056 | |||||||
chr16:1597120 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.370-4532A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597120 | |||||||
chr16:1597201 | T | TTCCCCAG others(3): Show |
1 | a0001c0001t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.370-4623_370-4614d others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597201 | |||||||
chr16:1597334 | C | T | 1 | a0001c0001t0002g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.370-4746G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597334 | |||||||
chr16:1597409 | G | C | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.370-4821C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597409 | |||||||
chr16:1597689 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.369+4681A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597689 | |||||||
chr16:1597772 | T | C | 2 | a0001c0004t0001g0074 a0001c0004t0001g0075 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.369+4598A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597772 | |||||||
chr16:1597812 | G | C | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+4558C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597812 | |||||||
chr16:1597827 | G | A | 1 | a0005c0009t0004g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.369+4543C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597827 | |||||||
chr16:1598125 | A | C | 151 | a0001c0001t0002g0174 a0001c0001t0003g0123 a0001c0002t0001g0005 others(148): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.369+4245T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598125 | |||||||
chr16:1598161 | T | C | 200 | a0001c0001t0002g0174 a0001c0001t0003g0038 a0001c0001t0003g0123 others(197): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+4209A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598161 | |||||||
chr16:1598319 | G | A | 1 | a0002c0003t0003g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369+4051C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598319 | |||||||
chr16:1598407 | G | A | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.369+3963C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598407 | |||||||
chr16:1598436 | C | T | 1 | a0003c0005t0003g0151 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.369+3934G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598436 | |||||||
chr16:1598544 | A | T | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369+3826T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598544 | |||||||
chr16:1598566 | T | C | 1 | a0001c0001t0002g0275 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.369+3804A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598566 | |||||||
chr16:1598637 | G | C | 215 | a0001c0001t0002g0174 a0001c0001t0002g0205 a0001c0001t0002g0230 others(212): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.369+3733C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598637 | |||||||
chr16:1598684 | G | C | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.369+3686C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598684 | |||||||
chr16:1598717 | C | T | 2 | a0001c0004t0001g0074 a0001c0004t0001g0075 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.369+3653G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598717 | |||||||
chr16:1598827 | G | A | 5 | a0001c0045t0002g0176 a0005c0009t0004g0166 a0005c0009t0004g0173 others(2): Show |
5 | HG02572.hp1 HG02630.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+3543C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598827 | |||||||
chr16:1598834 | A | AC | 10 | a0001c0001t0002g0294 a0001c0001t0002g0310 a0001c0002t0001g0086 others(7): Show |
10 | HG00544.hp2 HG01978.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.369+3535dupG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598834 | |||||||
chr16:1598879 | T | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0070 |
2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.369+3491A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598879 | |||||||
chr16:1598953 | C | CCATCTAG others(11): Show |
1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.369+3399_369+3416d others(20): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598953 | |||||||
chr16:1598972 | C | T | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.369+3398G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598972 | |||||||
chr16:1599040 | G | C | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.369+3330C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599040 | |||||||
chr16:1599065 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.369+3305G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599065 | |||||||
chr16:1599105 | G | C | 4 | a0001c0002t0001g0113 a0001c0004t0003g0112 a0001c0004t0003g0114 others(1): Show |
4 | NA18945.hp1 NA18975.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+3265C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599105 | |||||||
chr16:1599107 | C | A | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.369+3263G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599107 | |||||||
chr16:1599128 | C | T | 1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.369+3242G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599128 | |||||||
chr16:1599188 | A | G | 188 | a0001c0001t0002g0174 a0001c0001t0003g0038 a0001c0001t0003g0123 others(185): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.369+3182T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599188 | |||||||
chr16:1599216 | G | A | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.369+3154C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599216 | |||||||
chr16:1599252 | G | A | 6 | a0003c0005t0003g0063 a0007c0013t0001g0191 a0007c0013t0001g0192 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+3118C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599252 | |||||||
chr16:1599286 | A | G | 200 | a0001c0001t0002g0174 a0001c0001t0003g0038 a0001c0001t0003g0123 others(197): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+3084T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599286 | |||||||
chr16:1599309 | T | C | 1 | a0017c0055t0004g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369+3061A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599309 | |||||||
chr16:1599325 | G | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.369+3045C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599325 | |||||||
chr16:1599337 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.369+3033G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599337 | |||||||
chr16:1599357 | A | G | 3 | a0001c0001t0002g0261 a0001c0002t0001g0041 a0001c0054t0001g0119 |
3 | HG00639.hp1 HG01074.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.369+3013T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599357 | |||||||
chr16:1599392 | T | A | 1 | a0001c0001t0002g0261 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+2978A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599392 | |||||||
chr16:1599402 | T | C | 38 | a0001c0001t0002g0261 a0001c0001t0003g0038 a0002c0003t0003g0006 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.369+2968A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599402 | |||||||
chr16:1599403 | G | C | 1 | a0001c0001t0002g0261 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+2967C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | |||||||
chr16:1599403 | G | GCCGTCCG others(172): Show |
1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.369+2966_369+2967i others(181): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | |||||||
chr16:1599403 | G | GCCGTCCG others(170): Show |
136 | a0001c0001t0003g0123 a0001c0002t0001g0013 a0001c0002t0001g0041 others(133): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.369+2966_369+2967i others(179): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | |||||||
chr16:1599403 | G | GCCGTCCG others(171): Show |
4 | a0001c0002t0001g0005 a0001c0002t0001g0207 a0001c0002t0001g0224 others(1): Show |
4 | HG00544.hp2 HG02738.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+2966_369+2967i others(180): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | |||||||
chr16:1599403 | G | GTCGTCCG others(170): Show |
2 | a0001c0002t0001g0071 a0001c0002t0001g0095 |
2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.369+2966_369+2967i others(179): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | |||||||
chr16:1599406 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+2964C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599406 | |||||||
chr16:1599420 | T | TGGGGGGG others(171): Show |
1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.369+2949_369+2950i others(180): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599420 | |||||||
chr16:1599420 | T | TGGGGGGG others(172): Show |
1 | a0001c0002t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.369+2949_369+2950i others(181): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599420 | |||||||
chr16:1599421 | G | GGGGGGGT others(169): Show |
1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.369+2948_369+2949i others(178): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599421 | |||||||
chr16:1599430 | A | AGCCCCCC others(395): Show |
2 | a0001c0002t0005g0001 a0001c0002t0005g0002 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2939_369+2940i others(404): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599430 | |||||||
chr16:1599441 | T | C | 6 | a0001c0001t0002g0174 a0001c0001t0002g0307 a0001c0002t0001g0129 others(3): Show |
6 | HG01192.hp1 HG01516.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2929A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599441 | |||||||
chr16:1599451 | T | C | 152 | a0001c0001t0002g0174 a0001c0001t0002g0307 a0001c0001t0003g0123 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.369+2919A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599451 | |||||||
chr16:1599452 | G | C | 152 | a0001c0001t0002g0174 a0001c0001t0002g0307 a0001c0001t0003g0123 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.369+2918C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(493): Show |
2 | a0001c0010t0001g0125 a0001c0010t0001g0126 |
2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.369+2917_369+2918i others(502): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(925): Show |
1 | a0002c0003t0003g0034 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(934): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(727): Show |
1 | a0002c0003t0003g0026 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(736): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(919): Show |
1 | a0002c0003t0003g0036 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(493): Show |
1 | a0002c0003t0003g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(502): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(722): Show |
4 | a0002c0003t0003g0007 a0002c0003t0003g0009 a0024c0033t0003g0018 others(1): Show |
4 | NA18941.hp1 NA18959.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+2917_369+2918i others(731): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(820): Show |
1 | a0009c0011t0003g0044 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(829): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(918): Show |
11 | a0002c0003t0003g0017 a0002c0003t0003g0019 a0002c0003t0003g0022 others(8): Show |
11 | HG01071.hp1 HG02148.hp2 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+2917_369+2918i others(927): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(821): Show |
1 | a0009c0011t0003g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(830): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0016 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(919): Show |
6 | a0001c0001t0003g0038 a0002c0003t0003g0011 a0002c0003t0003g0015 others(3): Show |
6 | HG00642.hp2 HG01070.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2917_369+2918i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(922): Show |
1 | a0002c0003t0003g0032 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(931): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(822): Show |
1 | a0009c0011t0003g0045 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(831): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599452 | G | GCCGTCCG others(490): Show |
1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(499): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | |||||||
chr16:1599456 | T | TCCGGGAG others(706): Show |
1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.369+2913_369+2914i others(715): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599456 | |||||||
chr16:1599464 | G | GT | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2905_369+2906i others(3): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599464 | |||||||
chr16:1599468 | G | A | 146 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2902C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599468 | |||||||
chr16:1599469 | T | TGGGGGGG others(829): Show |
1 | a0009c0011t0003g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.369+2900_369+2901i others(838): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599469 | |||||||
chr16:1599469 | T | TGGGGGGG others(725): Show |
1 | a0002c0003t0003g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.369+2900_369+2901i others(734): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599469 | |||||||
chr16:1599469 | T | TGGGGGGG others(926): Show |
1 | a0002c0003t0003g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.369+2900_369+2901i others(935): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599469 | |||||||
chr16:1599473 | G | C | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2897C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599473 | |||||||
chr16:1599475 | G | C | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2895C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGGTCAGC others(812): Show |
1 | a0008c0021t0002g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(821): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGGTCAGC others(809): Show |
1 | a0001c0001t0002g0275 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(818): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0259 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(807): Show |
1 | a0001c0001t0002g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0330 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0331 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(807): Show |
1 | a0001c0001t0002g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0005c0009t0004g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0008c0021t0002g0315 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0004c0006t0002g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0278 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(758): Show |
1 | a0001c0001t0002g0310 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(767): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0017c0055t0004g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(810): Show |
1 | a0001c0001t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(819): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(807): Show |
1 | a0001c0001t0002g0289 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(808): Show |
1 | a0008c0046t0004g0258 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(817): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0001c0050t0002g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(755): Show |
3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(764): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0004g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0004c0006t0002g0327 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(756): Show |
1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(765): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0004c0006t0002g0313 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0004c0006t0002g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(757): Show |
1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(766): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0239 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
2 | a0012c0022t0002g0231 a0012c0022t0002g0236 |
2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
28 | a0001c0001t0002g0169 a0001c0001t0002g0178 a0001c0001t0002g0184 others(25): Show |
28 | HG00733.hp1 HG01123.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0297 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0235 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(807): Show |
1 | a0005c0009t0004g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0001c0001t0004g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
4 | a0001c0001t0002g0230 a0001c0001t0002g0234 a0001c0001t0002g0281 others(1): Show |
4 | HG00423.hp2 HG01081.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(755): Show |
3 | a0001c0001t0002g0264 a0001c0001t0002g0305 a0001c0001t0002g0306 |
3 | HG00099.hp1 HG01069.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(764): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
30 | a0001c0001t0002g0046 a0001c0001t0002g0227 a0001c0001t0002g0228 others(27): Show |
30 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(756): Show |
2 | a0001c0001t0002g0304 a0001c0001t0002g0309 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(765): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
8 | a0001c0001t0002g0240 a0001c0001t0002g0253 a0001c0001t0002g0274 others(5): Show |
8 | HG02071.hp2 HG02083.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0295 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(882): Show |
1 | a0004c0006t0002g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(891): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0332 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0029c0051t0004g0291 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0257 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599475 | G | T | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.369+2895C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | |||||||
chr16:1599476 | G | C | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2894C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599476 | |||||||
chr16:1599478 | C | CAGCCCCC others(805): Show |
1 | a0001c0010t0004g0238 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | |||||||
chr16:1599478 | C | CAGCCCCC others(806): Show |
1 | a0001c0001t0002g0319 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.369+2891_369+2892i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | |||||||
chr16:1599478 | C | CAGCCCCC others(806): Show |
1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | |||||||
chr16:1599478 | C | CAGCCCCC others(807): Show |
1 | a0001c0001t0002g0237 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.369+2891_369+2892i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | |||||||
chr16:1599478 | C | CAGCCCCC others(805): Show |
1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | |||||||
chr16:1599478 | C | CAGCCCCC others(723): Show |
1 | a0002c0003t0003g0008 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(732): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | |||||||
chr16:1599479 | G | A | 157 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(154): Show |
157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.369+2891C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599479 | |||||||
chr16:1599479 | G | T | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2891C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599479 | |||||||
chr16:1599480 | G | C | 6 | a0001c0001t0002g0237 a0001c0001t0002g0303 a0001c0001t0002g0319 others(3): Show |
6 | HG02135.hp1 HG02135.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2890C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599480 | |||||||
chr16:1599482 | C | CCGGCCGC others(20): Show |
2 | a0001c0001t0002g0174 a0003c0005t0001g0146 |
2 | HG01192.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2887_369+2888i others(29): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599482 | |||||||
chr16:1599484 | C | A | 1 | a0001c0004t0003g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.369+2886G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599484 | |||||||
chr16:1599484 | C | G | 1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369+2886G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599484 | |||||||
chr16:1599487 | G | A | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.369+2883C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599487 | |||||||
chr16:1599487 | G | GCCCCTAC others(23): Show |
1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369+2882_369+2883i others(32): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599487 | |||||||
chr16:1599499 | G | A | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2871C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599499 | |||||||
chr16:1599503 | C | T | 146 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2867G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599503 | |||||||
chr16:1599504 | G | GTCCGGGA others(923): Show |
1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.369+2865_369+2866i others(932): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | |||||||
chr16:1599504 | G | GTCCGGGA others(919): Show |
1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.369+2865_369+2866i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | |||||||
chr16:1599504 | G | GTCCGGGA others(920): Show |
1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.369+2865_369+2866i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | |||||||
chr16:1599504 | G | GTCCGGGA others(868): Show |
1 | a0011c0012t0003g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.369+2865_369+2866i others(877): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | |||||||
chr16:1599504 | G | GTCCGGGA others(918): Show |
4 | a0006c0007t0003g0161 a0006c0007t0003g0162 a0006c0007t0003g0199 others(1): Show |
4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+2865_369+2866i others(927): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | |||||||
chr16:1599504 | G | GTCCGGGA others(918): Show |
2 | a0011c0012t0003g0201 a0011c0012t0003g0202 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.369+2865_369+2866i others(927): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | |||||||
chr16:1599504 | G | GTCCGGGA others(919): Show |
1 | a0006c0007t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.369+2865_369+2866i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | |||||||
chr16:1599510 | G | T | 2 | a0001c0002t0001g0066 a0013c0023t0001g0060 |
2 | NA18970.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.369+2860C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599510 | |||||||
chr16:1599517 | G | A | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2853C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599517 | |||||||
chr16:1599518 | T | TG | 44 | a0001c0001t0002g0206 a0001c0001t0002g0239 a0001c0001t0002g0244 others(41): Show |
44 | HG00544.hp1 HG00642.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.369+2851dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599518 | |||||||
chr16:1599518 | TG | T | 20 | a0001c0001t0002g0255 a0001c0001t0002g0301 a0004c0006t0002g0204 others(17): Show |
20 | HG00733.hp1 HG00741.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.369+2851delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599518 | |||||||
chr16:1599518 | TGGG | T | 148 | a0001c0001t0002g0174 a0001c0001t0003g0123 a0001c0002t0001g0005 others(145): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.369+2849_369+2851d others(5): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599518 | |||||||
chr16:1599529 | T | C | 3 | a0001c0010t0001g0125 a0001c0010t0001g0126 a0020c0036t0003g0132 |
3 | HG03098.hp1 NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.369+2841A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599529 | |||||||
chr16:1599531 | A | G | 2 | a0001c0002t0005g0001 a0001c0002t0005g0002 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2839T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599531 | |||||||
chr16:1599536 | C | T | 146 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2834G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599536 | |||||||
chr16:1599538 | CT | C | 148 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(145): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.369+2831delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599538 | |||||||
chr16:1599539 | T | C | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2831A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599539 | |||||||
chr16:1599540 | G | A | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2830C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599540 | |||||||
chr16:1599541 | C | T | 146 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2829G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599541 | |||||||
chr16:1599542 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.369+2828G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599542 | |||||||
chr16:1599557 | G | A | 39 | a0001c0001t0003g0038 a0001c0002t0005g0001 a0001c0002t0005g0002 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.369+2813C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599557 | |||||||
chr16:1599560 | C | T | 146 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2810G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599560 | |||||||
chr16:1599561 | G | A | 2 | a0001c0002t0005g0001 a0001c0002t0005g0002 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2809C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599561 | |||||||
chr16:1599569 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2801T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599569 | |||||||
chr16:1599572 | G | T | 2 | a0001c0002t0001g0129 a0003c0005t0001g0146 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2798C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599572 | |||||||
chr16:1599573 | GCGCCTCT others(17): Show |
G | 2 | a0001c0002t0001g0129 a0003c0005t0001g0146 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2773_369+2796d others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599573 | |||||||
chr16:1599575 | G | C | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2795C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599575 | |||||||
chr16:1599577 | C | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2793G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599577 | |||||||
chr16:1599578 | T | C | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2792A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599578 | |||||||
chr16:1599582 | C | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2788G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599582 | |||||||
chr16:1599585 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2785C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599585 | |||||||
chr16:1599594 | T | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2776A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599594 | |||||||
chr16:1599595 | A | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2775T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599595 | |||||||
chr16:1599597 | T | C | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2773A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599597 | |||||||
chr16:1599601 | A | G | 2 | a0001c0002t0001g0129 a0003c0005t0001g0146 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2769T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599601 | |||||||
chr16:1599602 | A | G | 3 | a0001c0001t0002g0174 a0001c0002t0001g0129 a0003c0005t0001g0146 |
3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2768T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599602 | |||||||
chr16:1599605 | G | C | 2 | a0001c0002t0001g0129 a0003c0005t0001g0146 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2765C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599605 | |||||||
chr16:1599606 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2764T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599606 | |||||||
chr16:1599611 | C | CCCCCCCG others(91): Show |
2 | a0003c0005t0003g0148 a0007c0060t0001g0195 |
2 | HG00099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.369+2758_369+2759i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599611 | |||||||
chr16:1599615 | T | C | 148 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(145): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.369+2755A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599615 | |||||||
chr16:1599617 | T | C | 149 | a0001c0001t0002g0174 a0001c0001t0003g0123 a0001c0002t0001g0005 others(146): Show |
149 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.369+2753A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599617 | |||||||
chr16:1599618 | G | GCCCGGCC others(42): Show |
2 | a0001c0002t0005g0001 a0001c0002t0005g0002 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2751_369+2752i others(51): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599618 | |||||||
chr16:1599621 | C | T | 2 | a0001c0002t0001g0129 a0003c0005t0001g0146 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2749G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599621 | |||||||
chr16:1599634 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2736G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599634 | |||||||
chr16:1599638 | C | T | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.369+2732G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599638 | |||||||
chr16:1599648 | G | A | 2 | a0001c0002t0001g0129 a0003c0005t0001g0146 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2722C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599648 | |||||||
chr16:1599649 | T | TGGGGGGG others(175): Show |
1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.369+2720_369+2721i others(184): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | |||||||
chr16:1599649 | T | TGGGGGGG others(176): Show |
1 | a0001c0010t0001g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.369+2720_369+2721i others(185): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | |||||||
chr16:1599649 | T | TGGGGGGG others(565): Show |
1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2720_369+2721i others(574): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | |||||||
chr16:1599649 | TG | T | 11 | a0001c0001t0002g0174 a0001c0002t0001g0073 a0001c0002t0001g0096 others(8): Show |
11 | HG01192.hp1 HG02056.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+2720delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | |||||||
chr16:1599650 | G | GGGGGTGT others(91): Show |
3 | a0001c0002t0001g0071 a0001c0002t0001g0224 a0003c0031t0009g0140 |
3 | HG01081.hp1 HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.369+2719_369+2720i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | |||||||
chr16:1599650 | G | GGGGGTGT others(91): Show |
1 | a0001c0002t0001g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.369+2719_369+2720i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | |||||||
chr16:1599650 | G | GGGGGTGT others(90): Show |
129 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(126): Show |
129 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.369+2719_369+2720i others(99): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | |||||||
chr16:1599650 | G | GGGGGTGT others(91): Show |
1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.369+2719_369+2720i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | |||||||
chr16:1599656 | G | T | 10 | a0001c0002t0001g0073 a0001c0002t0001g0096 a0001c0002t0001g0207 others(7): Show |
10 | HG00741.hp1 HG02056.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.369+2714C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599656 | |||||||
chr16:1599659 | CA | C | 134 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(131): Show |
134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.369+2710delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599659 | |||||||
chr16:1599660 | A | G | 12 | a0001c0002t0001g0073 a0001c0002t0001g0096 a0001c0002t0001g0207 others(9): Show |
12 | HG00741.hp1 HG01175.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+2710T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599660 | |||||||
chr16:1599662 | C | CCCCCCGC others(90): Show |
1 | a0001c0002t0003g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.369+2707_369+2708i others(99): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599662 | |||||||
chr16:1599662 | C | G | 134 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(131): Show |
134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.369+2708G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599662 | |||||||
chr16:1599666 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2704G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599666 | |||||||
chr16:1599668 | C | G | 34 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.369+2702G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599668 | |||||||
chr16:1599668 | C | T | 3 | a0001c0010t0001g0125 a0001c0010t0001g0126 a0020c0036t0003g0132 |
3 | HG03098.hp1 NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.369+2702G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599668 | |||||||
chr16:1599670 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2700G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599670 | |||||||
chr16:1599685 | C | T | 2 | a0001c0002t0001g0129 a0003c0005t0001g0146 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2685G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599685 | |||||||
chr16:1599686 | G | A | 137 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(134): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.369+2684C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599686 | |||||||
chr16:1599689 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2681G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599689 | |||||||
chr16:1599690 | G | A | 137 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(134): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.369+2680C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | |||||||
chr16:1599690 | G | GGGAGGGA others(269): Show |
1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369+2679_369+2680i others(278): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | |||||||
chr16:1599690 | G | GGGAGGGA others(268): Show |
1 | a0003c0005t0001g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.369+2679_369+2680i others(277): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | |||||||
chr16:1599690 | G | GGGAGGGA others(92): Show |
1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.369+2679_369+2680i others(101): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | |||||||
chr16:1599690 | G | GGGAGGGA others(91): Show |
6 | a0001c0002t0001g0073 a0001c0002t0001g0096 a0001c0002t0001g0207 others(3): Show |
6 | HG02056.hp1 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2679_369+2680i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | |||||||
chr16:1599690 | G | GGGAGGGA others(91): Show |
2 | a0003c0005t0001g0143 a0003c0005t0001g0147 |
2 | HG03017.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.369+2679_369+2680i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | |||||||
chr16:1599713 | C | T | 2 | a0001c0001t0002g0324 a0001c0001t0002g0325 |
2 | NA18945.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.369+2657G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599713 | |||||||
chr16:1599759 | G | T | 188 | a0001c0001t0002g0174 a0001c0001t0003g0038 a0001c0001t0003g0123 others(185): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.369+2611C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599759 | |||||||
chr16:1599795 | C | G | 1 | a0002c0003t0003g0019 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.369+2575G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599795 | |||||||
chr16:1599796 | G | A | 107 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.369+2574C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599796 | |||||||
chr16:1599799 | C | T | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2571G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599799 | |||||||
chr16:1599800 | G | A | 12 | a0001c0002t0001g0223 a0006c0007t0003g0159 a0006c0007t0003g0160 others(9): Show |
12 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.369+2570C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599800 | |||||||
chr16:1599817 | A | G | 200 | a0001c0001t0002g0174 a0001c0001t0003g0038 a0001c0001t0003g0123 others(197): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+2553T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599817 | |||||||
chr16:1599827 | T | TG | 200 | a0001c0001t0002g0174 a0001c0001t0002g0310 a0001c0001t0003g0038 others(197): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+2542dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599827 | |||||||
chr16:1599867 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2503C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599867 | |||||||
chr16:1599910 | T | C | 9 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(6): Show |
9 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+2460A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599910 | |||||||
chr16:1599966 | T | C | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.369+2404A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599966 | |||||||
chr16:1600316 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.369+2054C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600316 | |||||||
chr16:1600460 | AT | A | 12 | a0001c0001t0002g0200 a0001c0002t0001g0071 a0001c0002t0001g0072 others(9): Show |
12 | HG01081.hp1 HG02015.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+1909delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600460 | |||||||
chr16:1600462 | T | TA | 7 | a0001c0001t0002g0174 a0001c0001t0002g0245 a0001c0001t0002g0254 others(4): Show |
7 | HG01109.hp1 HG01255.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+1907_369+1908i others(3): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600462 | |||||||
chr16:1600462 | TTA | T | 43 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0011 others(40): Show |
43 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.369+1906_369+1907d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600462 | |||||||
chr16:1600463 | T | A | 17 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0184 others(14): Show |
17 | HG01070.hp1 HG01109.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+1907A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | |||||||
chr16:1600463 | T | TA | 47 | a0001c0001t0002g0178 a0001c0001t0002g0180 a0001c0001t0002g0181 others(44): Show |
47 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.369+1906dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | |||||||
chr16:1600463 | TA | T | 136 | a0001c0001t0002g0318 a0001c0001t0003g0123 a0001c0002t0001g0005 others(133): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.369+1906delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | |||||||
chr16:1600463 | TAA | T | 6 | a0001c0002t0001g0066 a0001c0002t0001g0196 a0001c0004t0001g0117 others(3): Show |
6 | HG01884.hp2 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1905_369+1906d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | |||||||
chr16:1600465 | A | T | 1 | a0001c0002t0001g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.369+1905T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600465 | |||||||
chr16:1600617 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.369+1753C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600617 | |||||||
chr16:1600685 | G | A | 3 | a0001c0002t0001g0080 a0001c0004t0003g0081 a0027c0041t0001g0062 |
3 | NA18961.hp2 NA19005.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.369+1685C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600685 | |||||||
chr16:1600730 | T | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.369+1640A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600730 | |||||||
chr16:1600905 | A | G | 1 | a0002c0003t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.369+1465T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600905 | |||||||
chr16:1600906 | G | A | 1 | a0013c0023t0001g0060 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.369+1464C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600906 | |||||||
chr16:1600936 | T | A | 1 | a0013c0023t0001g0060 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.369+1434A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600936 | |||||||
chr16:1600945 | A | G | 268 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0178 others(265): Show |
268 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.369+1425T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600945 | |||||||
chr16:1600978 | A | T | 1 | a0002c0003t0003g0022 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.369+1392T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600978 | |||||||
chr16:1601079 | A | G | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.369+1291T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601079 | |||||||
chr16:1601167 | G | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.369+1203C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601167 | |||||||
chr16:1601257 | C | T | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.369+1113G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601257 | |||||||
chr16:1601263 | CA | C | 6 | a0001c0001t0002g0174 a0001c0001t0002g0245 a0001c0001t0002g0259 others(3): Show |
6 | HG02735.hp1 HG03041.hp2 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1106delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601263 | |||||||
chr16:1601290 | A | G | 1 | a0001c0004t0003g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.369+1080T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601290 | |||||||
chr16:1601593 | G | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+777C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601593 | |||||||
chr16:1601880 | G | A | 11 | a0001c0002t0001g0047 a0001c0002t0001g0049 a0001c0002t0001g0068 others(8): Show |
11 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.369+490C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601880 | |||||||
chr16:1602192 | C | T | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.369+178G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1602192 | |||||||
chr16:1602226 | T | C | 2 | a0001c0002t0001g0333 a0001c0002t0001g0334 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.369+144A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1602226 | |||||||
chr16:1602613 | T | A | 197 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(194): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.148-22A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602613 | |||||||
chr16:1602620 | A | G | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.148-29T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602620 | |||||||
chr16:1602664 | G | A | 13 | a0001c0002t0001g0311 a0002c0003t0003g0032 a0006c0007t0003g0159 others(10): Show |
13 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-73C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602664 | |||||||
chr16:1602812 | C | T | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-221G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602812 | |||||||
chr16:1602828 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.148-237A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602828 | |||||||
chr16:1602921 | C | A | 1 | a0001c0004t0003g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.148-330G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602921 | |||||||
chr16:1602998 | G | A | 6 | a0003c0005t0003g0063 a0007c0013t0001g0191 a0007c0013t0001g0192 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-407C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602998 | |||||||
chr16:1603067 | C | T | 1 | a0003c0005t0003g0151 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.148-476G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603067 | |||||||
chr16:1603205 | C | T | 197 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(194): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.148-614G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603205 | |||||||
chr16:1603222 | C | G | 4 | a0009c0011t0003g0042 a0009c0011t0003g0043 a0009c0011t0003g0044 others(1): Show |
4 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-631G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603222 | |||||||
chr16:1603259 | C | T | 3 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0002g0250 |
3 | NA18953.hp2 NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.148-668G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603259 | |||||||
chr16:1603577 | A | G | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.148-986T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603577 | |||||||
chr16:1603630 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.148-1039C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603630 | |||||||
chr16:1603641 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.148-1050G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603641 | |||||||
chr16:1603708 | C | A | 1 | a0001c0002t0001g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.148-1117G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603708 | |||||||
chr16:1603733 | G | A | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-1142C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603733 | |||||||
chr16:1603770 | C | T | 1 | a0004c0006t0002g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.148-1179G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603770 | |||||||
chr16:1603777 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.148-1186C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603777 | |||||||
chr16:1603863 | C | T | 9 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(6): Show |
9 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-1272G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603863 | |||||||
chr16:1604193 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.148-1602G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604193 | |||||||
chr16:1604264 | G | A | 39 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0003g0038 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.148-1673C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604264 | |||||||
chr16:1604274 | C | CGT | 42 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0002t0001g0103 others(39): Show |
42 | HG00408.hp2 HG00673.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.148-1685_148-1684d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGT | 53 | a0001c0001t0002g0004 a0001c0001t0002g0279 a0001c0001t0002g0280 others(50): Show |
53 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.148-1687_148-1684d others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGT | 43 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0271 others(40): Show |
43 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.148-1689_148-1684d others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(1): Show |
46 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0182 others(43): Show |
46 | HG00280.hp2 HG00408.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.148-1691_148-1684d others(10): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(3): Show |
29 | a0001c0001t0002g0174 a0001c0001t0002g0250 a0001c0001t0002g0252 others(26): Show |
29 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.148-1693_148-1684d others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(5): Show |
20 | a0001c0001t0002g0200 a0001c0001t0002g0303 a0001c0001t0002g0304 others(17): Show |
20 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.148-1695_148-1684d others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(7): Show |
10 | a0001c0001t0002g0206 a0001c0001t0002g0245 a0001c0001t0002g0248 others(7): Show |
10 | HG01070.hp1 HG01081.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.148-1697_148-1684d others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(9): Show |
13 | a0001c0001t0002g0240 a0001c0001t0002g0244 a0001c0001t0004g0170 others(10): Show |
13 | HG01109.hp2 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-1699_148-1684d others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(11): Show |
12 | a0001c0001t0002g0169 a0001c0001t0002g0233 a0001c0001t0002g0234 others(9): Show |
12 | HG01099.hp2 HG01361.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.148-1701_148-1684d others(20): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(13): Show |
7 | a0001c0001t0002g0228 a0001c0001t0002g0230 a0001c0001t0002g0232 others(4): Show |
7 | HG00642.hp1 HG02148.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-1703_148-1684d others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(15): Show |
3 | a0001c0001t0002g0205 a0004c0006t0002g0204 a0011c0012t0003g0051 |
3 | HG01256.hp1 HG03209.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.148-1705_148-1684d others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | C | CGTGTGTG others(17): Show |
2 | a0001c0001t0002g0227 a0001c0001t0002g0301 |
2 | HG02257.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.148-1707_148-1684d others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | CGT | C | 13 | a0001c0001t0002g0293 a0001c0002t0001g0120 a0001c0002t0001g0121 others(10): Show |
13 | HG02083.hp2 HG02109.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-1685_148-1684d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | CGTGT | C | 14 | a0001c0001t0002g0184 a0001c0020t0003g0138 a0001c0020t0003g0139 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.148-1687_148-1684d others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | CGTGTGTG others(5): Show |
C | 2 | a0003c0005t0001g0156 a0003c0005t0001g0157 |
2 | NA19057.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.148-1695_148-1684d others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604274 | CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0294 |
2 | HG03490.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.148-1697_148-1684d others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | |||||||
chr16:1604298 | TGTGTGTG others(13): Show |
T | 1 | a0001c0001t0004g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.148-1727_148-1708d others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604298 | |||||||
chr16:1604304 | TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0002g0290 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.148-1727_148-1714d others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604304 | |||||||
chr16:1604306 | TGTGTGTG others(5): Show |
T | 1 | a0029c0051t0004g0291 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.148-1727_148-1716d others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604306 | |||||||
chr16:1604318 | G | T | 39 | a0001c0001t0002g0205 a0001c0001t0002g0230 a0001c0001t0002g0234 others(36): Show |
39 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.148-1727C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604318 | |||||||
chr16:1604335 | T | TGAGG | 196 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(193): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.148-1745_148-1744i others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604335 | |||||||
chr16:1604336 | A | G | 1 | a0028c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.148-1745T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604336 | |||||||
chr16:1604386 | A | G | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.148-1795T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604386 | |||||||
chr16:1604436 | T | G | 1 | a0001c0001t0002g0295 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.148-1845A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604436 | |||||||
chr16:1604444 | C | T | 2 | a0011c0012t0003g0201 a0011c0012t0003g0202 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.148-1853G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604444 | |||||||
chr16:1604524 | C | G | 1 | a0001c0004t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.148-1933G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604524 | |||||||
chr16:1604524 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.148-1933G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604524 | |||||||
chr16:1604752 | C | A | 197 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(194): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.148-2161G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604752 | |||||||
chr16:1604780 | G | A | 2 | a0001c0001t0002g0296 a0001c0001t0002g0297 |
2 | NA18991.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.148-2189C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604780 | |||||||
chr16:1604945 | G | A | 159 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(156): Show |
159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.147+2175C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604945 | |||||||
chr16:1604947 | G | A | 148 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(145): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.147+2173C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604947 | |||||||
chr16:1605031 | C | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.147+2089G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605031 | |||||||
chr16:1605072 | T | C | 4 | a0009c0011t0003g0042 a0009c0011t0003g0043 a0009c0011t0003g0044 others(1): Show |
4 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2048A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605072 | |||||||
chr16:1605198 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147+1922C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605198 | |||||||
chr16:1605278 | A | T | 2 | a0008c0021t0002g0315 a0008c0021t0002g0316 |
2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.147+1842T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605278 | |||||||
chr16:1605353 | T | C | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147+1767A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605353 | |||||||
chr16:1605356 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.147+1764C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605356 | |||||||
chr16:1605396 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.147+1724G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605396 | |||||||
chr16:1605438 | C | T | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.147+1682G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605438 | |||||||
chr16:1605443 | T | C | 1 | a0003c0005t0001g0157 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.147+1677A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605443 | |||||||
chr16:1605605 | C | T | 4 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0019t0003g0136 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+1515G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605605 | |||||||
chr16:1605758 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.147+1362C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605758 | |||||||
chr16:1605896 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.147+1224C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605896 | |||||||
chr16:1606015 | G | A | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.147+1105C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606015 | |||||||
chr16:1606216 | G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.147+904C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606216 | |||||||
chr16:1606229 | C | A | 2 | a0001c0001t0002g0299 a0001c0001t0002g0300 |
2 | HG01081.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.147+891G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606229 | |||||||
chr16:1606255 | G | A | 1 | a0028c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.147+865C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606255 | |||||||
chr16:1606320 | G | A | 32 | a0003c0005t0001g0141 a0003c0005t0001g0142 a0003c0005t0001g0143 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.147+800C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606320 | |||||||
chr16:1606395 | C | A | 1 | a0001c0001t0002g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147+725G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606395 | |||||||
chr16:1606438 | A | C | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.147+682T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606438 | |||||||
chr16:1606506 | G | T | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.147+614C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606506 | |||||||
chr16:1606531 | G | A | 1 | a0026c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+589C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606531 | |||||||
chr16:1606563 | C | T | 1 | a0001c0002t0010g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.147+557G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606563 | |||||||
chr16:1606564 | G | A | 2 | a0007c0013t0001g0194 a0007c0060t0001g0195 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.147+556C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606564 | |||||||
chr16:1606622 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.147+498C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606622 | |||||||
chr16:1606632 | G | T | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.147+488C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606632 | |||||||
chr16:1606764 | A | G | 201 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(198): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.147+356T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606764 | |||||||
chr16:1606866 | C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.147+254G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606866 | |||||||
chr16:1606928 | A | G | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+192T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606928 | |||||||
chr16:1606935 | C | T | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+185G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606935 | |||||||
chr16:1607011 | C | T | 109 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.147+109G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1607011 | |||||||
chr16:1607033 | CAT | C | 37 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(34): Show |
37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.147+85_147+86delAT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1607033 | |||||||
chr16:1607349 | A | T | 158 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(155): Show |
158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-31-52T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607349 | |||||||
chr16:1607426 | C | T | 1 | a0006c0007t0003g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-31-129G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607426 | |||||||
chr16:1607510 | C | A | 1 | a0020c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31-213G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607510 | |||||||
chr16:1607753 | C | T | 109 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-31-456G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607753 | |||||||
chr16:1607834 | C | A | 1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-31-537G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607834 | |||||||
chr16:1607852 | C | T | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-31-555G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607852 | |||||||
chr16:1607976 | C | T | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-679G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607976 | |||||||
chr16:1608032 | A | C | 1 | a0001c0010t0004g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-31-735T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608032 | |||||||
chr16:1608055 | T | C | 201 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(198): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-31-758A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608055 | |||||||
chr16:1608085 | G | C | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-31-788C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608085 | |||||||
chr16:1608100 | TAG | T | 146 | a0001c0001t0003g0123 a0001c0002t0001g0005 a0001c0002t0001g0013 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-31-805_-31-804del others(2): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608100 | |||||||
chr16:1608153 | C | G | 201 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(198): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-31-856G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608153 | |||||||
chr16:1608333 | G | T | 1 | a0001c0002t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-31-1036C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608333 | |||||||
chr16:1608391 | G | A | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-1094C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608391 | |||||||
chr16:1608418 | T | C | 6 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-1121A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608418 | |||||||
chr16:1608453 | C | T | 37 | a0001c0001t0003g0038 a0002c0003t0003g0006 a0002c0003t0003g0007 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-31-1156G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608453 | |||||||
chr16:1608526 | C | T | 5 | a0007c0013t0001g0191 a0007c0013t0001g0192 a0007c0013t0001g0193 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-1229G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608526 | |||||||
chr16:1608631 | C | CA | 110 | a0001c0001t0002g0184 a0001c0001t0002g0303 a0001c0001t0002g0304 others(107): Show |
110 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-31-1335dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608631 | |||||||
chr16:1608631 | C | CAA | 44 | a0001c0002t0001g0128 a0001c0002t0001g0129 a0001c0002t0001g0131 others(41): Show |
44 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-31-1336_-31-1335d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608631 | |||||||
chr16:1608631 | CA | C | 6 | a0005c0009t0004g0166 a0005c0009t0004g0167 a0011c0012t0003g0051 others(3): Show |
6 | HG01070.hp1 HG02258.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-1335delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608631 | |||||||
chr16:1608926 | C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-1629G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608926 | |||||||
chr16:1609127 | T | C | 201 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(198): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-32+1537A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609127 | |||||||
chr16:1609722 | T | G | 37 | a0001c0020t0003g0138 a0001c0020t0003g0139 a0003c0005t0001g0141 others(34): Show |
37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-32+942A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609722 | |||||||
chr16:1609856 | C | A | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+808G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609856 | |||||||
chr16:1609857 | T | G | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+807A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609857 | |||||||
chr16:1609960 | C | T | 7 | a0003c0017t0001g0058 a0003c0017t0001g0059 a0010c0015t0003g0053 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32+704G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609960 | |||||||
chr16:1610075 | T | A | 2 | a0001c0001t0002g0324 a0001c0001t0002g0325 |
2 | NA18945.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-32+589A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610075 | |||||||
chr16:1610088 | T | C | 2 | a0004c0006t0002g0313 a0004c0026t0004g0312 |
2 | HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-32+576A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610088 | |||||||
chr16:1610121 | GC | G | 3 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0009 |
3 | NA18941.hp1 NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-32+542delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610121 | |||||||
chr16:1610127 | C | T | 1 | a0001c0001t0002g0314 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-32+537G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610127 | |||||||
chr16:1610152 | CG | C | 12 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0001c0001t0002g0318 others(9): Show |
12 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32+511delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610152 | |||||||
chr16:1610206 | T | C | 11 | a0006c0007t0003g0159 a0006c0007t0003g0160 a0006c0007t0003g0161 others(8): Show |
11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+458A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610206 | |||||||
chr16:1610263 | T | A | 1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-32+401A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610263 | |||||||
chr16:1610273 | A | G | 200 | a0001c0001t0003g0038 a0001c0001t0003g0123 a0001c0002t0001g0005 others(197): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-32+391T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610273 | |||||||
chr16:1610285 | G | T | 2 | a0011c0012t0003g0051 a0011c0012t0003g0052 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-32+379C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610285 | |||||||
chr16:1610612 | G | C | 1 | a0001c0004t0003g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-32+52C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610612 | |||||||
chr16:1610923 | T | G | 1 | a0001c0001t0003g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-221-70A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1610923 | |||||||
chr16:1610938 | C | T | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-221-85G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1610938 | |||||||
chr16:1610993 | C | A | 1 | a0008c0040t0003g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-221-140G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1610993 | |||||||
chr16:1611167 | G | A | 3 | a0002c0003t0003g0006 a0002c0003t0003g0039 a0002c0003t0003g0040 |
3 | NA18950.hp2 NA18990.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-221-314C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611167 | |||||||
chr16:1611169 | G | A | 1 | a0028c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-221-316C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611169 | |||||||
chr16:1611280 | G | C | 1 | a0001c0004t0003g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-221-427C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611280 | |||||||
chr16:1611293 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-221-440G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611293 | |||||||
chr16:1611490 | C | CA | 24 | a0001c0001t0002g0200 a0001c0001t0002g0329 a0001c0001t0002g0330 others(21): Show |
24 | HG01074.hp2 HG01109.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-222+477dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611490 | |||||||
chr16:1611490 | CA | C | 8 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0002t0001g0005 others(5): Show |
8 | HG01256.hp1 HG02895.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+477delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611490 | |||||||
chr16:1611620 | G | C | 2 | a0011c0012t0003g0201 a0011c0012t0003g0202 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+348C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611620 | |||||||
chr16:1611700 | A | G | 202 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0178 others(199): Show |
202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.-222+268T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611700 | |||||||
chr16:1611741 | G | C | 2 | a0001c0002t0001g0333 a0001c0002t0001g0334 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-222+227C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611741 | |||||||
chr16:1611813 | CA | C | 42 | a0001c0001t0002g0046 a0001c0001t0003g0038 a0001c0002t0001g0005 others(39): Show |
42 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-222+154delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611813 | |||||||
chr16:1611825 | A | G | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-222+143T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611825 |