Item | Value |
---|---|
geneid | 80173 |
ensemblid | ENSG00000096872.17 |
hgncid | 21424 |
symbol | IFT74 |
name | intraflagellar transport 74 |
refseq_nuc | NM_025103.4 |
refseq_prot | NP_079379.2 |
ensembl_nuc | ENST00000380062.10 |
ensembl_prot | ENSP00000369402.5 |
mane_status | MANE Select |
chr | chr9 |
start | 26956412 |
end | 27066134 |
strand | + |
ver | v1.2 |
region | chr9:26956412-27066134 |
region5000 | chr9:26951412-27071134 |
regionname0 | IFT74_chr9_26956412_27066134 |
regionname5000 | IFT74_chr9_26951412_27071134 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 600 | 200 | 66 | 37 | 60 | 9 | 26 | 43 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0002 | 0/0 | 600 | 64 | 1 | 15 | 45 | 0 | 3 | 35 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0003 | 0/0 | 600 | 25 | 8 | 3 | 11 | 0 | 3 | 9 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0004 | 0/0 | 600 | 14 | 0 | 4 | 5 | 1 | 4 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0005 | 0/0 | 600 | 14 | 2 | 2 | 3 | 0 | 7 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0006 | 0/0 | 600 | 13 | 5 | 3 | 0 | 2 | 3 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0007 | 0/0 | 600 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0008 | 0/0 | 600 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0009 | 0/0 | 600 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0010 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0011 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
a0012 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | MASNH others(595): Show |
chr9 | 26951412 | 27071134 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1800 | 196 | 66 | 33 | 60 | 9 | 26 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0001c0008 | 0/0 | 1800 | 3 | 0 | 3 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0001c0012 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0002c0002 | 0/0 | 1800 | 64 | 1 | 15 | 45 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0003c0003 | 0/0 | 1800 | 25 | 8 | 3 | 11 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0004c0004 | 0/0 | 1800 | 14 | 0 | 4 | 5 | 1 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0005c0005 | 0/0 | 1800 | 14 | 2 | 2 | 3 | 0 | 7 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0006c0006 | 0/0 | 1800 | 13 | 5 | 3 | 0 | 2 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0007c0007 | 0/0 | 1800 | 7 | 5 | 2 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0008c0011 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0009c0014 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0010c0013 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0011c0010 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 | ||
a0012c0009 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | ATGGC others(1795): Show |
chr9 | 26951412 | 27071134 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5325 | 142 | 41 | 16 | 54 | 6 | 23 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0002 | 0/0 | 5325 | 4 | 2 | 1 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0003 | 0/0 | 5325 | 22 | 2 | 14 | 0 | 3 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0007 | 0/0 | 5325 | 5 | 4 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0009 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0010 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0011 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0013 | 0/0 | 5325 | 2 | 0 | 0 | 2 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0014 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0015 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0016 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0018 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0020 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0025 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0028 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0029 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0030 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0032 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0033 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0034 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0001t0035 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0008t0001 | 0/0 | 5325 | 3 | 0 | 3 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0001c0012t0003 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0002c0002t0002 | 0/0 | 5325 | 63 | 1 | 14 | 45 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0002c0002t0024 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0003c0003t0002 | 0/0 | 5325 | 20 | 6 | 3 | 9 | 0 | 2 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0003c0003t0006 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0003c0003t0021 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0003c0003t0022 | 0/0 | 5325 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0003c0003t0027 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0004c0004t0004 | 0/0 | 5313 | 13 | 0 | 3 | 5 | 1 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5308): Show |
chr9 | 26951412 | 27071134 |
a0004c0004t0036 | 0/0 | 5313 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5308): Show |
chr9 | 26951412 | 27071134 |
a0005c0005t0005 | 0/0 | 5313 | 12 | 0 | 2 | 3 | 0 | 7 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5308): Show |
chr9 | 26951412 | 27071134 |
a0005c0005t0012 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5308): Show |
chr9 | 26951412 | 27071134 |
a0006c0006t0001 | 0/0 | 5325 | 12 | 4 | 3 | 0 | 2 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0006c0006t0026 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0007c0007t0006 | 0/0 | 5325 | 3 | 2 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0007c0007t0008 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0007c0007t0019 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0007c0007t0023 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0008c0011t0001 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0009c0014t0003 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0010c0013t0031 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0011c0010t0017 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
a0012c0009t0008 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | AGTTA others(5320): Show |
chr9 | 26951412 | 27071134 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0013g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0014g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0016g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0020g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0025g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0028g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0029g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0030g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0032g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0033g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0034g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0001t0035g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0008t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0008t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0001c0012t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0002c0002t0024g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0021g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0022g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0003c0003t0027g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0004c0004t0036g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0012g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0005c0005t0012g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0006c0006t0026g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0007c0007t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0007c0007t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0007c0007t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0007c0007t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0007c0007t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0007c0007t0019g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0007c0007t0023g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0008c0011t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0009c0014t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0010c0013t0031g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0011c0010t0017g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
a0012c0009t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0282 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0296 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0304 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00323 | hp2 | a0004 | c0004 | t0004 | g0021 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00408 | hp1 | a0003 | c0003 | t0002 | g0127 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00639 | hp2 | a0005 | c0005 | t0005 | g0309 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00733 | hp1 | a0007 | c0007 | t0006 | g0026 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00733 | hp2 | a0004 | c0004 | t0004 | g0024 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00735 | hp1 | a0001 | c0012 | t0003 | g0301 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00735 | hp2 | a0002 | c0002 | t0024 | g0319 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01069 | hp2 | a0006 | c0006 | t0001 | g0324 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01070 | hp2 | a0006 | c0006 | t0001 | g0333 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0172 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01167 | hp2 | a0003 | c0003 | t0002 | g0112 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0111 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0295 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01192 | hp2 | a0001 | c0008 | t0001 | g0170 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01255 | hp2 | a0007 | c0007 | t0019 | g0119 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01256 | hp1 | a0005 | c0005 | t0005 | g0310 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0294 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01257 | hp1 | a0006 | c0006 | t0001 | g0331 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01358 | hp2 | a0001 | c0008 | t0001 | g0169 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01361 | hp2 | a0004 | c0004 | t0036 | g0029 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01496 | hp2 | a0004 | c0004 | t0004 | g0025 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01515 | hp1 | a0006 | c0006 | t0001 | g0329 | EUR | IBS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01891 | hp1 | a0001 | c0001 | t0030 | g0110 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01891 | hp2 | a0003 | c0003 | t0002 | g0323 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0058 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01934 | hp1 | a0004 | c0004 | t0004 | g0019 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0049 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01975 | hp2 | a0008 | c0011 | t0001 | g0236 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0057 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0291 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01993 | hp1 | a0001 | c0008 | t0001 | g0171 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01993 | hp2 | a0009 | c0014 | t0003 | g0292 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02055 | hp1 | a0003 | c0003 | t0006 | g0114 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02055 | hp2 | a0006 | c0006 | t0026 | g0207 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02056 | hp2 | a0004 | c0004 | t0004 | g0015 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02080 | hp1 | a0001 | c0001 | t0029 | g0159 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02145 | hp2 | a0006 | c0006 | t0001 | g0335 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | CDX | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02258 | hp1 | a0006 | c0006 | t0001 | g0328 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02258 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02273 | hp1 | a0001 | c0001 | t0016 | g0293 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0095 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0060 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02300 | hp1 | a0003 | c0003 | t0002 | g0101 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02523 | hp2 | a0003 | c0003 | t0002 | g0039 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02572 | hp2 | a0001 | c0001 | t0015 | g0131 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02615 | hp1 | a0007 | c0007 | t0008 | g0005 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02630 | hp2 | a0007 | c0007 | t0006 | g0017 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02683 | hp1 | a0006 | c0006 | t0001 | g0327 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02683 | hp2 | a0003 | c0003 | t0002 | g0088 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02717 | hp1 | a0005 | c0005 | t0012 | g0340 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02717 | hp2 | a0006 | c0006 | t0001 | g0326 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02723 | hp2 | a0003 | c0003 | t0002 | g0320 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02735 | hp2 | a0005 | c0005 | t0005 | g0311 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02738 | hp2 | a0005 | c0005 | t0005 | g0317 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02886 | hp1 | a0003 | c0003 | t0002 | g0321 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02886 | hp2 | a0001 | c0001 | t0033 | g0105 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02895 | hp1 | a0003 | c0003 | t0006 | g0113 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02922 | hp1 | a0001 | c0001 | t0025 | g0177 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03098 | hp1 | a0001 | c0001 | t0015 | g0132 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03130 | hp2 | a0003 | c0003 | t0002 | g0050 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03139 | hp1 | a0003 | c0003 | t0002 | g0322 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03209 | hp2 | a0007 | c0007 | t0023 | g0006 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03239 | hp1 | a0004 | c0004 | t0004 | g0020 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03239 | hp2 | a0005 | c0005 | t0005 | g0307 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03486 | hp1 | a0001 | c0001 | t0034 | g0141 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03486 | hp2 | a0001 | c0001 | t0035 | g0243 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03491 | hp2 | a0004 | c0004 | t0004 | g0018 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03540 | hp1 | a0001 | c0001 | t0018 | g0128 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0135 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03579 | hp2 | a0007 | c0007 | t0008 | g0004 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03654 | hp1 | a0005 | c0005 | t0005 | g0318 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03688 | hp2 | a0003 | c0003 | t0022 | g0055 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03704 | hp2 | a0004 | c0004 | t0004 | g0276 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0076 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03834 | hp1 | a0005 | c0005 | t0005 | g0308 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03834 | hp2 | a0003 | c0003 | t0002 | g0038 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03927 | hp1 | a0006 | c0006 | t0001 | g0332 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04199 | hp1 | a0005 | c0005 | t0005 | g0312 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04228 | hp1 | a0006 | c0006 | t0001 | g0334 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18957 | hp1 | a0005 | c0005 | t0005 | g0314 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18959 | hp2 | a0001 | c0001 | t0013 | g0266 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18960 | hp1 | a0001 | c0001 | t0013 | g0267 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18960 | hp2 | a0004 | c0004 | t0004 | g0014 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18964 | hp1 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18965 | hp2 | a0005 | c0005 | t0005 | g0315 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18973 | hp1 | a0004 | c0004 | t0004 | g0028 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18973 | hp2 | a0003 | c0003 | t0002 | g0089 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18975 | hp1 | a0003 | c0003 | t0002 | g0091 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18984 | hp2 | a0004 | c0004 | t0004 | g0022 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18989 | hp2 | a0004 | c0004 | t0004 | g0016 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18994 | hp1 | a0005 | c0005 | t0005 | g0316 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18994 | hp2 | a0003 | c0003 | t0002 | g0093 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19010 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0033 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19030 | hp2 | a0011 | c0010 | t0017 | g0115 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19066 | hp1 | a0001 | c0001 | t0032 | g0225 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0090 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19077 | hp1 | a0003 | c0003 | t0027 | g0099 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19081 | hp1 | a0001 | c0001 | t0020 | g0152 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19081 | hp2 | a0003 | c0003 | t0021 | g0100 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19090 | hp1 | a0003 | c0003 | t0002 | g0098 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19240 | hp1 | a0012 | c0009 | t0008 | g0003 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA19240 | hp2 | a0005 | c0005 | t0012 | g0339 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20129 | hp1 | a0003 | c0003 | t0002 | g0043 | AFR | ASW | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ASW | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | TSI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20752 | hp2 | a0006 | c0006 | t0001 | g0330 | EUR | TSI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20905 | hp1 | a0004 | c0004 | t0004 | g0023 | SAS | GIH | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20905 | hp2 | a0005 | c0005 | t0005 | g0313 | SAS | GIH | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0281 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02109 | hp2 | a0001 | c0001 | t0028 | g0300 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02559 | hp1 | a0006 | c0006 | t0001 | g0325 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG02559 | hp2 | a0010 | c0013 | t0031 | g0284 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
HG06807 | hp2 | a0007 | c0007 | t0006 | g0027 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0202 | REF | REF | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0145 | REF | REF | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26962001 | C | T | 1 | a0009 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.34C>T | p.Pro12Ser | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/20 | 158/5325 | 34/1803 | 12/600 | chr9 | 26962001 | |||
chr9:26978159 | G | A | 1 | a0012 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.152G>A | p.Arg51His | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/20 | 276/5325 | 152/1803 | 51/600 | chr9 | 26978159 | |||
chr9:26978172 | A | G | 1 | a0002 | 64 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
missense_variant | MODERATE | c.165A>G | p.Ile55Met | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/20 | 289/5325 | 165/1803 | 55/600 | chr9 | 26978172 | |||
chr9:26978261 | A | G | 2 | a0002 a0003 |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
missense_variant&splice_region_variant | MODERATE | c.254A>G | p.Lys85Arg | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/20 | 378/5325 | 254/1803 | 85/600 | chr9 | 26978261 | |||
chr9:26984279 | A | G | 1 | a0006 | 13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
missense_variant | MODERATE | c.328A>G | p.Thr110Ala | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/20 | 452/5325 | 328/1803 | 110/600 | chr9 | 26984279 | |||
chr9:27009097 | T | C | 1 | a0011 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.665T>C | p.Met222Thr | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/20 | 789/5325 | 665/1803 | 222/600 | chr9 | 27009097 | |||
chr9:27009102 | T | C | 3 | a0004 a0007 a0012 |
22 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(19): Show |
missense_variant | MODERATE | c.670T>C | p.Phe224Leu | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/20 | 794/5325 | 670/1803 | 224/600 | chr9 | 27009102 | |||
chr9:27016910 | A | G | 1 | a0010 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.793A>G | p.Ile265Val | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/20 | 917/5325 | 793/1803 | 265/600 | chr9 | 27016910 | |||
chr9:27055618 | G | A | 1 | a0008 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.1343G>A | p.Arg448His | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/20 | 1467/5325 | 1343/1803 | 448/600 | chr9 | 27055618 | |||
chr9:27062723 | C | T | 2 | a0004 a0005 |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
missense_variant | MODERATE | c.1790C>T | p.Thr597Ile | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1914/5325 | 1790/1803 | 597/600 | chr9 | 27062723 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26984311 | A | G | 1 | a0001c0008 | 3 | HG01192.hp2 HG01358.hp2 HG01993.hp1 |
synonymous_variant | LOW | c.360A>G | p.Glu120Glu | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/20 | 484/5325 | 360/1803 | 120/600 | chr9 | 26984311 | |||
chr9:27056378 | C | T | 1 | a0001c0012 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1542C>T | p.Ala514Ala | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/20 | 1666/5325 | 1542/1803 | 514/600 | chr9 | 27056378 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26956434 | C | T | 1 | a0004c0004t0036 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/20 | 5534 | chr9 | 26956434 | ||||||
chr9:26956487 | G | A | 1 | a0001c0001t0016 | 1 | HG02273.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/20 | 5481 | chr9 | 26956487 | ||||||
chr9:26956505 | G | A | 3 | a0001c0001t0018 a0007c0007t0019 a0011c0010t0017 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-31G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/20 | 5463 | chr9 | 26956505 | ||||||
chr9:26961954 | A | G | 1 | a0001c0001t0035 | 1 | HG03486.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-14A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/20 | chr9 | 26961954 | |||||||
chr9:27062792 | C | A | 1 | a0001c0001t0020 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 56 | chr9 | 27062792 | ||||||
chr9:27063177 | T | C | 23 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(20): Show |
138 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*441T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 441 | chr9 | 27063177 | ||||||
chr9:27063376 | G | A | 1 | a0001c0001t0028 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 640 | chr9 | 27063376 | ||||||
chr9:27063510 | G | A | 1 | a0001c0001t0029 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 774 | chr9 | 27063510 | ||||||
chr9:27063578 | C | A | 1 | a0001c0001t0009 | 2 | HG03041.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 842 | chr9 | 27063578 | ||||||
chr9:27063666 | T | C | 1 | a0001c0001t0013 | 2 | NA18959.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*930T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 930 | chr9 | 27063666 | ||||||
chr9:27063697 | A | G | 2 | a0007c0007t0008 a0012c0009t0008 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*961A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 961 | chr9 | 27063697 | ||||||
chr9:27063736 | C | T | 1 | a0001c0001t0034 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1000C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1000 | chr9 | 27063736 | ||||||
chr9:27063840 | T | C | 1 | a0001c0001t0014 | 2 | HG02258.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1104T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1104 | chr9 | 27063840 | ||||||
chr9:27063847 | G | A | 1 | a0001c0001t0007 | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1111G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1111 | chr9 | 27063847 | ||||||
chr9:27063857 | C | T | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1121C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1121 | chr9 | 27063857 | ||||||
chr9:27063894 | C | G | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1158C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1158 | chr9 | 27063894 | ||||||
chr9:27063998 | C | T | 1 | a0001c0001t0015 | 2 | HG02572.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1262C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1262 | chr9 | 27063998 | ||||||
chr9:27063999 | G | A | 1 | a0001c0001t0007 | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1263G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1263 | chr9 | 27063999 | ||||||
chr9:27064017 | G | A | 2 | a0004c0004t0004 a0004c0004t0036 |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1281G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1281 | chr9 | 27064017 | ||||||
chr9:27064025 | T | A | 1 | a0001c0001t0030 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1289T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1289 | chr9 | 27064025 | ||||||
chr9:27064055 | A | G | 1 | a0003c0003t0027 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1319 | chr9 | 27064055 | ||||||
chr9:27064333 | T | G | 2 | a0003c0003t0021 a0003c0003t0027 |
2 | NA19077.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1597T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1597 | chr9 | 27064333 | ||||||
chr9:27064400 | G | A | 6 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(3): Show |
27 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1664 | chr9 | 27064400 | ||||||
chr9:27064572 | A | T | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1836A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1836 | chr9 | 27064572 | ||||||
chr9:27064608 | A | G | 2 | a0003c0003t0006 a0007c0007t0006 |
5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1872A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1872 | chr9 | 27064608 | ||||||
chr9:27064730 | T | C | 1 | a0003c0003t0022 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1994T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1994 | chr9 | 27064730 | ||||||
chr9:27064732 | A | G | 1 | a0005c0005t0012 | 2 | HG02717.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1996A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1996 | chr9 | 27064732 | ||||||
chr9:27064757 | G | A | 4 | a0001c0001t0009 a0007c0007t0008 a0007c0007t0023 others(1): Show |
6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2021G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2021 | chr9 | 27064757 | ||||||
chr9:27064792 | CCCTTTTA others(5): Show |
C | 4 | a0004c0004t0004 a0004c0004t0036 a0005c0005t0005 others(1): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2059_*2070delTTTT others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2059 | INFO_REALIGN_3_PRIME | chr9 | 27064792 | |||||
chr9:27064840 | T | A | 1 | a0002c0002t0024 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2104T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2104 | chr9 | 27064840 | ||||||
chr9:27064959 | C | A | 1 | a0001c0001t0010 | 2 | HG01884.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2223C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2223 | chr9 | 27064959 | ||||||
chr9:27065169 | T | A | 4 | a0001c0001t0009 a0007c0007t0008 a0007c0007t0023 others(1): Show |
6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2433T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2433 | chr9 | 27065169 | ||||||
chr9:27065194 | G | A | 1 | a0001c0001t0025 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2458G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2458 | chr9 | 27065194 | ||||||
chr9:27065199 | A | C | 1 | a0010c0013t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2463 | chr9 | 27065199 | ||||||
chr9:27065297 | C | T | 1 | a0001c0001t0018 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2561C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2561 | chr9 | 27065297 | ||||||
chr9:27065385 | G | A | 2 | a0001c0001t0010 a0001c0001t0011 |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2649G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2649 | chr9 | 27065385 | ||||||
chr9:27065494 | G | C | 1 | a0001c0001t0011 | 2 | HG02451.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2758G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2758 | chr9 | 27065494 | ||||||
chr9:27065656 | T | G | 1 | a0001c0001t0032 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2920T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2920 | chr9 | 27065656 | ||||||
chr9:27065781 | A | G | 1 | a0006c0006t0026 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3045A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 3045 | chr9 | 27065781 | ||||||
chr9:27066072 | T | C | 4 | a0004c0004t0004 a0004c0004t0036 a0005c0005t0005 others(1): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3336T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 3336 | chr9 | 27066072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26956551 | C | T | 2 | a0005c0005t0012g0339 a0005c0005t0012g0340 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+35C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956551 | |||||||
chr9:26956563 | G | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20+47G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956563 | |||||||
chr9:26956580 | A | C | 15 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(12): Show |
15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+64A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956580 | |||||||
chr9:26956655 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+139C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956655 | |||||||
chr9:26956664 | A | T | 1 | a0002c0002t0024g0319 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-20+148A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956664 | |||||||
chr9:26956665 | C | T | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+149C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956665 | |||||||
chr9:26956704 | C | G | 1 | a0001c0001t0001g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-20+188C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956704 | |||||||
chr9:26956725 | AC | A | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+215delC | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26956725 | ||||||
chr9:26956761 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+245G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956761 | |||||||
chr9:26956770 | G | A | 161 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(158): Show |
161 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-20+254G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956770 | |||||||
chr9:26956807 | T | C | 7 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(4): Show |
7 | HG00621.hp1 NA18959.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+291T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956807 | |||||||
chr9:26956834 | T | C | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+318T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956834 | |||||||
chr9:26956860 | C | T | 1 | a0004c0004t0036g0029 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-20+344C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956860 | |||||||
chr9:26956870 | C | G | 104 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(101): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-20+354C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956870 | |||||||
chr9:26956881 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0306 |
2 | HG00609.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-20+365T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956881 | |||||||
chr9:26956906 | T | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20+390T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956906 | |||||||
chr9:26957093 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-20+577A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957093 | |||||||
chr9:26957117 | C | G | 1 | a0004c0004t0004g0028 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-20+601C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957117 | |||||||
chr9:26957152 | C | A | 20 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20+636C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957152 | |||||||
chr9:26957235 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-20+719T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957235 | |||||||
chr9:26957700 | A | C | 2 | a0001c0001t0015g0131 a0001c0001t0015g0132 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-20+1184A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957700 | |||||||
chr9:26957799 | C | CT | 8 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0018g0128 others(5): Show |
8 | HG00408.hp1 HG01496.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+1295dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26957799 | ||||||
chr9:26957863 | G | A | 1 | a0002c0002t0002g0030 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-20+1347G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957863 | |||||||
chr9:26957913 | A | C | 193 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(190): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-20+1397A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957913 | |||||||
chr9:26958050 | G | A | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+1534G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958050 | |||||||
chr9:26958246 | G | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+1730G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958246 | |||||||
chr9:26958371 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+1855C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958371 | |||||||
chr9:26958441 | C | G | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+1925C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958441 | |||||||
chr9:26958457 | C | G | 4 | a0002c0002t0002g0123 a0002c0002t0002g0124 a0002c0002t0002g0125 others(1): Show |
4 | NA18991.hp2 NA19002.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1941C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958457 | |||||||
chr9:26958659 | T | A | 1 | a0004c0004t0004g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-20+2143T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958659 | |||||||
chr9:26958670 | T | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+2154T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958670 | |||||||
chr9:26958730 | G | C | 81 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(78): Show |
81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.-20+2214G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958730 | |||||||
chr9:26958764 | G | A | 1 | a0002c0002t0002g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-20+2248G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958764 | |||||||
chr9:26958924 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+2408G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958924 | |||||||
chr9:26959089 | T | TTTG | 97 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(94): Show |
97 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-20+2606_-20+2608d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | ||||||
chr9:26959089 | T | TTTGTTG | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0007g0135 others(4): Show |
7 | HG02523.hp2 HG02723.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+2603_-20+2608d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | ||||||
chr9:26959089 | T | TTTGTTGT others(2): Show |
13 | a0001c0001t0015g0131 a0001c0001t0015g0132 a0005c0005t0005g0307 others(10): Show |
13 | HG00639.hp2 HG01256.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+2600_-20+2608d others(11): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | ||||||
chr9:26959089 | TTTG | T | 26 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(23): Show |
26 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-20+2606_-20+2608d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | ||||||
chr9:26959089 | TTTGTTG | T | 9 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 others(6): Show |
9 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+2603_-20+2608d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | ||||||
chr9:26959139 | C | T | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.-20+2623C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959139 | |||||||
chr9:26959159 | A | T | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.-20+2643A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959159 | |||||||
chr9:26959181 | T | C | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+2665T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959181 | |||||||
chr9:26959269 | C | T | 1 | a0004c0004t0036g0029 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19-2680C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959269 | |||||||
chr9:26959303 | G | A | 1 | a0006c0006t0026g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-19-2646G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959303 | |||||||
chr9:26959383 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-19-2566G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959383 | |||||||
chr9:26959400 | C | T | 2 | a0003c0003t0006g0113 a0003c0003t0006g0114 |
2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-19-2549C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959400 | |||||||
chr9:26959916 | A | G | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-2033A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959916 | |||||||
chr9:26959988 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-19-1961G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959988 | |||||||
chr9:26960087 | A | G | 157 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(154): Show |
157 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-19-1862A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960087 | |||||||
chr9:26960122 | T | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-19-1827T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960122 | |||||||
chr9:26960228 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-19-1721A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960228 | |||||||
chr9:26960290 | G | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-19-1659G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960290 | |||||||
chr9:26960320 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-1629T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960320 | |||||||
chr9:26960405 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-19-1544A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960405 | |||||||
chr9:26960525 | T | G | 6 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(3): Show |
6 | HG01069.hp1 HG01175.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-1424T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960525 | |||||||
chr9:26961018 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19-931C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961018 | |||||||
chr9:26961051 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-898G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961051 | |||||||
chr9:26961083 | G | GT | 36 | a0001c0001t0001g0118 a0001c0001t0001g0197 a0001c0001t0001g0198 others(33): Show |
36 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-19-848dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26961083 | ||||||
chr9:26961083 | G | GTT | 16 | a0001c0001t0009g0032 a0001c0001t0010g0034 a0001c0001t0010g0035 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-849_-19-848dup others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26961083 | ||||||
chr9:26961108 | G | A | 75 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0204 others(72): Show |
75 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-19-841G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961108 | |||||||
chr9:26961109 | G | T | 84 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(81): Show |
84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19-840G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961109 | |||||||
chr9:26961125 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-19-824G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961125 | |||||||
chr9:26961225 | G | C | 84 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(81): Show |
84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19-724G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961225 | |||||||
chr9:26961257 | A | AT | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-686dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26961257 | ||||||
chr9:26961306 | G | T | 1 | a0003c0003t0002g0039 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-643G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961306 | |||||||
chr9:26961312 | C | G | 330 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(327): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-19-637C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961312 | |||||||
chr9:26961435 | C | A | 20 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0211 others(17): Show |
20 | HG00423.hp2 HG02129.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-514C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961435 | |||||||
chr9:26961476 | T | C | 1 | a0003c0003t0027g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-19-473T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961476 | |||||||
chr9:26961575 | C | G | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-19-374C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961575 | |||||||
chr9:26961622 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-19-327A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961622 | |||||||
chr9:26961749 | G | T | 2 | a0001c0001t0018g0128 a0007c0007t0019g0119 |
2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-19-200G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961749 | |||||||
chr9:26961838 | C | T | 15 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(12): Show |
15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-111C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961838 | |||||||
chr9:26961893 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-56T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961893 | |||||||
chr9:26962172 | C | A | 93 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(90): Show |
93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.120+85C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962172 | |||||||
chr9:26962407 | C | A | 20 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.120+320C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962407 | |||||||
chr9:26962462 | T | G | 1 | a0002c0002t0002g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.120+375T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962462 | |||||||
chr9:26962490 | A | G | 34 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(31): Show |
34 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.120+403A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962490 | |||||||
chr9:26962671 | G | C | 1 | a0005c0005t0005g0307 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.120+584G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962671 | |||||||
chr9:26962771 | A | G | 34 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(31): Show |
34 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.120+684A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962771 | |||||||
chr9:26962845 | A | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+758A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962845 | |||||||
chr9:26962872 | T | C | 15 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(12): Show |
15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+785T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962872 | |||||||
chr9:26962926 | A | AT | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+852dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962926 | ||||||
chr9:26962926 | AT | A | 61 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0120 others(58): Show |
61 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.120+852delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962926 | ||||||
chr9:26962926 | ATT | A | 13 | a0001c0001t0001g0151 a0001c0001t0001g0201 a0006c0006t0001g0324 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+851_120+852del others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962926 | ||||||
chr9:26962930 | T | TTTTC | 86 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(83): Show |
86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.120+846_120+847ins others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962930 | ||||||
chr9:26962930 | T | TTTTTC | 19 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(16): Show |
19 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+847_120+848ins others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962930 | ||||||
chr9:26963090 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.120+1003C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963090 | |||||||
chr9:26963113 | C | G | 1 | a0001c0001t0025g0177 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120+1026C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963113 | |||||||
chr9:26963113 | C | T | 1 | a0002c0002t0002g0012 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.120+1026C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963113 | |||||||
chr9:26963123 | A | G | 1 | a0001c0001t0032g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.120+1036A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963123 | |||||||
chr9:26963131 | C | A | 88 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.120+1044C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963131 | |||||||
chr9:26963204 | C | T | 1 | a0006c0006t0026g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.120+1117C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963204 | |||||||
chr9:26963229 | G | A | 164 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(161): Show |
164 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.120+1142G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963229 | |||||||
chr9:26963303 | A | G | 1 | a0002c0002t0002g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.120+1216A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963303 | |||||||
chr9:26963304 | T | C | 1 | a0002c0002t0002g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.120+1217T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963304 | |||||||
chr9:26963407 | C | T | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+1320C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963407 | |||||||
chr9:26963618 | CTGT | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+1536_120+1538d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26963618 | ||||||
chr9:26963670 | G | A | 108 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(105): Show |
108 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.120+1583G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963670 | |||||||
chr9:26963688 | C | T | 33 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(30): Show |
33 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.120+1601C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963688 | |||||||
chr9:26963715 | A | G | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.120+1628A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963715 | |||||||
chr9:26963742 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.120+1655C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963742 | |||||||
chr9:26963752 | G | A | 1 | a0006c0006t0001g0324 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.120+1665G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963752 | |||||||
chr9:26963763 | G | A | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1676G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963763 | |||||||
chr9:26963772 | G | T | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1685G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963772 | |||||||
chr9:26963776 | G | C | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1689G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963776 | |||||||
chr9:26963844 | A | G | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+1757A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963844 | |||||||
chr9:26963916 | G | C | 3 | a0001c0001t0011g0033 a0001c0001t0011g0036 a0007c0007t0023g0006 |
3 | HG02451.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.120+1829G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963916 | |||||||
chr9:26963969 | G | T | 2 | a0001c0001t0001g0224 a0003c0003t0006g0113 |
2 | HG02895.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.120+1882G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963969 | |||||||
chr9:26964000 | G | A | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+1913G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964000 | |||||||
chr9:26964011 | T | C | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+1924T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964011 | |||||||
chr9:26964079 | G | C | 84 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(81): Show |
84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.120+1992G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964079 | |||||||
chr9:26964104 | G | A | 17 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(14): Show |
17 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.120+2017G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964104 | |||||||
chr9:26964110 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.120+2023G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964110 | |||||||
chr9:26964178 | A | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+2091A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964178 | |||||||
chr9:26964211 | T | G | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.120+2124T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964211 | |||||||
chr9:26964230 | C | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+2143C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964230 | |||||||
chr9:26964285 | GT | G | 88 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.120+2200delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26964285 | ||||||
chr9:26964439 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+2352C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964439 | |||||||
chr9:26964582 | C | T | 8 | a0003c0003t0002g0039 a0003c0003t0002g0089 a0003c0003t0002g0090 others(5): Show |
8 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+2495C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964582 | |||||||
chr9:26964617 | GT | G | 6 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0001c0001t0010g0034 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+2532delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26964617 | ||||||
chr9:26964739 | C | T | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+2652C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964739 | |||||||
chr9:26964801 | T | C | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+2714T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964801 | |||||||
chr9:26965356 | T | G | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.120+3269T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965356 | |||||||
chr9:26965399 | G | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.120+3312G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965399 | |||||||
chr9:26965469 | G | C | 13 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(10): Show |
13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.120+3382G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965469 | |||||||
chr9:26965524 | G | A | 1 | a0001c0001t0020g0152 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.120+3437G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965524 | |||||||
chr9:26965683 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.120+3596A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965683 | |||||||
chr9:26965687 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+3600A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965687 | |||||||
chr9:26965707 | G | C | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.120+3620G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965707 | |||||||
chr9:26965810 | T | C | 28 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(25): Show |
28 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.120+3723T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965810 | |||||||
chr9:26965855 | C | G | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+3768C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965855 | |||||||
chr9:26966022 | G | T | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.120+3935G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966022 | |||||||
chr9:26966067 | C | T | 33 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(30): Show |
33 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.120+3980C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966067 | |||||||
chr9:26966207 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+4120A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966207 | |||||||
chr9:26966301 | A | G | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+4214A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966301 | |||||||
chr9:26966438 | C | T | 1 | a0001c0001t0010g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.120+4351C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966438 | |||||||
chr9:26966445 | G | A | 156 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(153): Show |
156 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.120+4358G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966445 | |||||||
chr9:26966476 | T | C | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+4389T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966476 | |||||||
chr9:26966554 | A | T | 109 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.120+4467A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966554 | |||||||
chr9:26966561 | A | G | 15 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(12): Show |
15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+4474A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966561 | |||||||
chr9:26966722 | G | C | 1 | a0002c0002t0002g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.120+4635G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966722 | |||||||
chr9:26966761 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.120+4674G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966761 | |||||||
chr9:26966901 | A | G | 1 | a0003c0003t0002g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.120+4814A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966901 | |||||||
chr9:26967063 | A | G | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.120+4976A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967063 | |||||||
chr9:26967142 | T | A | 1 | a0002c0002t0002g0042 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.120+5055T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967142 | |||||||
chr9:26967375 | C | A | 1 | a0001c0001t0003g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.120+5288C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967375 | |||||||
chr9:26967381 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.120+5294T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967381 | |||||||
chr9:26967404 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+5317G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967404 | |||||||
chr9:26967478 | A | G | 329 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(326): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.120+5391A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967478 | |||||||
chr9:26967787 | G | A | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+5700G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967787 | |||||||
chr9:26967825 | G | C | 2 | a0005c0005t0005g0307 a0005c0005t0005g0308 |
2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.120+5738G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967825 | |||||||
chr9:26967884 | T | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+5797T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967884 | |||||||
chr9:26967977 | C | T | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+5890C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967977 | |||||||
chr9:26968025 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.120+5938G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968025 | |||||||
chr9:26968066 | CT | C | 65 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(62): Show |
65 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.120+5996delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968066 | ||||||
chr9:26968066 | CTT | C | 85 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
85 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.120+5995_120+5996d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968066 | ||||||
chr9:26968077 | T | A | 33 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(30): Show |
33 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.120+5990T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968077 | |||||||
chr9:26968122 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+6035G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968122 | |||||||
chr9:26968139 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.120+6052A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968139 | |||||||
chr9:26968256 | TA | T | 15 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(12): Show |
15 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+6178delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968256 | ||||||
chr9:26968265 | AT | A | 147 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(144): Show |
147 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.120+6192delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968265 | ||||||
chr9:26968286 | T | G | 329 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(326): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.120+6199T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968286 | |||||||
chr9:26968324 | C | CT | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+6237_120+6238i others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968324 | |||||||
chr9:26968326 | A | C | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+6239A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968326 | |||||||
chr9:26968346 | C | T | 15 | a0002c0002t0002g0077 a0002c0002t0002g0078 a0002c0002t0002g0079 others(12): Show |
15 | HG00558.hp2 HG00609.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+6259C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968346 | |||||||
chr9:26968364 | C | T | 1 | a0003c0003t0002g0101 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.120+6277C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968364 | |||||||
chr9:26968365 | G | A | 1 | a0003c0003t0002g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.120+6278G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968365 | |||||||
chr9:26968410 | T | C | 109 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.120+6323T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968410 | |||||||
chr9:26968432 | T | G | 23 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0178 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.120+6345T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968432 | |||||||
chr9:26968434 | A | G | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.120+6347A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968434 | |||||||
chr9:26968517 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+6430C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968517 | |||||||
chr9:26968672 | T | C | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+6585T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968672 | |||||||
chr9:26968700 | T | C | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.120+6613T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968700 | |||||||
chr9:26968802 | C | CT | 28 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 others(25): Show |
29 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.120+6722dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968802 | ||||||
chr9:26968833 | T | G | 1 | a0001c0001t0011g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.120+6746T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968833 | |||||||
chr9:26968836 | T | C | 15 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(12): Show |
15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+6749T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968836 | |||||||
chr9:26968862 | C | G | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+6775C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968862 | |||||||
chr9:26968890 | AT | A | 161 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(158): Show |
161 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.120+6811delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968890 | ||||||
chr9:26969115 | G | T | 7 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0003g0296 others(4): Show |
7 | HG00280.hp1 HG00323.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+7028G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969115 | |||||||
chr9:26969179 | C | G | 1 | a0001c0001t0003g0299 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.120+7092C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969179 | |||||||
chr9:26969182 | G | A | 28 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(25): Show |
28 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.120+7095G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969182 | |||||||
chr9:26969212 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.120+7125C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969212 | |||||||
chr9:26969253 | T | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+7166T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969253 | |||||||
chr9:26969324 | A | C | 13 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(10): Show |
13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.120+7237A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969324 | |||||||
chr9:26969351 | C | T | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+7264C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969351 | |||||||
chr9:26969381 | T | C | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+7294T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969381 | |||||||
chr9:26969459 | T | A | 165 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(162): Show |
165 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.120+7372T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969459 | |||||||
chr9:26969512 | T | A | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+7425T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969512 | |||||||
chr9:26969565 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120+7478T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969565 | |||||||
chr9:26969771 | G | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+7684G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969771 | |||||||
chr9:26969787 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+7700A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969787 | |||||||
chr9:26969938 | C | T | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+7851C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969938 | |||||||
chr9:26969939 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+7852G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969939 | |||||||
chr9:26969993 | C | T | 20 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0211 others(17): Show |
20 | HG00423.hp2 HG02129.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.120+7906C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969993 | |||||||
chr9:26970059 | C | A | 2 | a0006c0006t0001g0325 a0006c0006t0001g0326 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.120+7972C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970059 | |||||||
chr9:26970129 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.121-7999C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970129 | |||||||
chr9:26970364 | T | C | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.121-7764T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970364 | |||||||
chr9:26970386 | A | T | 109 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.121-7742A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970386 | |||||||
chr9:26970561 | A | G | 3 | a0001c0008t0001g0169 a0001c0008t0001g0170 a0001c0008t0001g0171 |
3 | HG01192.hp2 HG01358.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.121-7567A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970561 | |||||||
chr9:26970656 | T | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-7472T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970656 | |||||||
chr9:26970819 | A | G | 1 | a0006c0006t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121-7309A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970819 | |||||||
chr9:26970835 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-7293G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970835 | |||||||
chr9:26970949 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121-7179G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970949 | |||||||
chr9:26970965 | A | G | 1 | a0001c0001t0028g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121-7163A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970965 | |||||||
chr9:26971121 | C | T | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121-7007C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971121 | |||||||
chr9:26971128 | G | A | 2 | a0003c0003t0006g0113 a0003c0003t0006g0114 |
2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.121-7000G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971128 | |||||||
chr9:26971300 | G | C | 1 | a0003c0003t0002g0089 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.121-6828G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971300 | |||||||
chr9:26971366 | A | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-6762A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971366 | |||||||
chr9:26971438 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG02895.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121-6690C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971438 | |||||||
chr9:26971558 | G | T | 4 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-6570G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971558 | |||||||
chr9:26971580 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.121-6548C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971580 | |||||||
chr9:26971634 | A | G | 1 | a0010c0013t0031g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.121-6494A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971634 | |||||||
chr9:26971816 | T | C | 2 | a0003c0003t0006g0113 a0003c0003t0006g0114 |
2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.121-6312T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971816 | |||||||
chr9:26971854 | A | C | 1 | a0006c0006t0001g0333 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.121-6274A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971854 | |||||||
chr9:26971898 | A | G | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.121-6230A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971898 | |||||||
chr9:26972016 | C | G | 1 | a0006c0006t0001g0332 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.121-6112C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972016 | |||||||
chr9:26972256 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.121-5872C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972256 | |||||||
chr9:26972347 | A | G | 2 | a0001c0001t0015g0131 a0001c0001t0015g0132 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.121-5781A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972347 | |||||||
chr9:26972432 | G | A | 1 | a0002c0002t0002g0044 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.121-5696G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972432 | |||||||
chr9:26972502 | G | C | 1 | a0008c0011t0001g0236 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.121-5626G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972502 | |||||||
chr9:26972558 | G | C | 23 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(20): Show |
23 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.121-5570G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972558 | |||||||
chr9:26973112 | G | A | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-5016G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973112 | |||||||
chr9:26973121 | C | T | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121-5007C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973121 | |||||||
chr9:26973168 | A | T | 1 | a0002c0002t0002g0030 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.121-4960A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973168 | |||||||
chr9:26973186 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.121-4942G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973186 | |||||||
chr9:26973210 | C | T | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.121-4918C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973210 | |||||||
chr9:26973362 | A | G | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-4766A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973362 | |||||||
chr9:26973527 | G | A | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.121-4601G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973527 | |||||||
chr9:26973635 | C | A | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.121-4493C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973635 | |||||||
chr9:26973655 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-4473G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973655 | |||||||
chr9:26973677 | A | T | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.121-4451A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973677 | |||||||
chr9:26973787 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0020g0152 |
2 | HG02056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.121-4341G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973787 | |||||||
chr9:26974056 | C | T | 2 | a0003c0003t0021g0100 a0003c0003t0027g0099 |
2 | NA19077.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.121-4072C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974056 | |||||||
chr9:26974099 | A | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-4029A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974099 | |||||||
chr9:26974123 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0306 |
2 | NA18969.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.121-4005C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974123 | |||||||
chr9:26974124 | G | A | 10 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0001c0001t0003g0294 others(7): Show |
10 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-4004G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974124 | |||||||
chr9:26974247 | G | T | 231 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(228): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.121-3881G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974247 | |||||||
chr9:26974419 | A | G | 2 | a0005c0005t0012g0339 a0005c0005t0012g0340 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.121-3709A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974419 | |||||||
chr9:26974524 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.121-3604T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974524 | |||||||
chr9:26974693 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-3435C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974693 | |||||||
chr9:26974839 | A | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-3289A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974839 | |||||||
chr9:26974862 | C | A | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-3266C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974862 | |||||||
chr9:26975079 | T | TA | 88 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.121-3048dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26975079 | ||||||
chr9:26975134 | G | A | 88 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.121-2994G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975134 | |||||||
chr9:26975151 | G | T | 90 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(87): Show |
90 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.121-2977G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975151 | |||||||
chr9:26975280 | T | G | 1 | a0006c0006t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121-2848T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975280 | |||||||
chr9:26975285 | A | G | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-2843A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975285 | |||||||
chr9:26975426 | A | T | 17 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.121-2702A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975426 | |||||||
chr9:26975439 | G | A | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.121-2689G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975439 | |||||||
chr9:26975440 | G | A | 1 | a0006c0006t0026g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121-2688G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975440 | |||||||
chr9:26975469 | A | G | 13 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(10): Show |
13 | HG01192.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.121-2659A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975469 | |||||||
chr9:26975520 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.121-2608C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975520 | |||||||
chr9:26975570 | G | A | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-2558G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975570 | |||||||
chr9:26975599 | C | T | 81 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(78): Show |
81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.121-2529C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975599 | |||||||
chr9:26975647 | T | C | 12 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(9): Show |
12 | HG00639.hp2 HG01256.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-2481T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975647 | |||||||
chr9:26975657 | C | T | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.121-2471C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975657 | |||||||
chr9:26975951 | T | G | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121-2177T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975951 | |||||||
chr9:26976045 | C | T | 1 | a0001c0001t0016g0293 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.121-2083C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976045 | |||||||
chr9:26976088 | C | T | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-2040C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976088 | |||||||
chr9:26976257 | G | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-1871G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976257 | |||||||
chr9:26976296 | G | A | 6 | a0003c0003t0002g0321 a0003c0003t0002g0322 a0004c0004t0004g0018 others(3): Show |
6 | HG00733.hp2 HG01934.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-1832G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976296 | |||||||
chr9:26976298 | A | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0305 |
3 | HG01243.hp1 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.121-1830A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976298 | |||||||
chr9:26976446 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-1682C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976446 | |||||||
chr9:26976492 | A | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0305 |
3 | HG01243.hp1 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.121-1636A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976492 | |||||||
chr9:26976679 | A | C | 1 | a0003c0003t0002g0101 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.121-1449A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976679 | |||||||
chr9:26976879 | T | C | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.121-1249T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976879 | |||||||
chr9:26976881 | G | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-1247G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976881 | |||||||
chr9:26976913 | T | C | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-1215T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976913 | |||||||
chr9:26977030 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.121-1098A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977030 | |||||||
chr9:26977169 | G | A | 88 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.121-959G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977169 | |||||||
chr9:26977313 | T | A | 109 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.121-815T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977313 | |||||||
chr9:26977331 | T | C | 109 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.121-797T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977331 | |||||||
chr9:26977366 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-762G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977366 | |||||||
chr9:26977562 | C | A | 31 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 others(28): Show |
32 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.121-566C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977562 | |||||||
chr9:26977567 | C | T | 1 | a0005c0005t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.121-561C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977567 | |||||||
chr9:26977689 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.121-439A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977689 | |||||||
chr9:26977712 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-416C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977712 | |||||||
chr9:26977769 | G | A | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-359G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977769 | |||||||
chr9:26977788 | T | G | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.121-340T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977788 | |||||||
chr9:26977804 | A | G | 30 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(27): Show |
30 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.121-324A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977804 | |||||||
chr9:26977813 | A | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.121-315A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977813 | |||||||
chr9:26977954 | A | G | 1 | a0006c0006t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121-174A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977954 | |||||||
chr9:26978004 | A | G | 2 | a0002c0002t0002g0074 a0002c0002t0002g0075 |
2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.121-124A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26978004 | |||||||
chr9:26978050 | T | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-78T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26978050 | |||||||
chr9:26978305 | T | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.256+42T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978305 | |||||||
chr9:26978389 | T | A | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+126T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978389 | |||||||
chr9:26978462 | G | A | 1 | a0005c0005t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.256+199G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978462 | |||||||
chr9:26978552 | T | C | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.256+289T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978552 | |||||||
chr9:26978627 | A | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0200 |
3 | HG02135.hp1 NA19007.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.256+364A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978627 | |||||||
chr9:26978710 | A | G | 7 | a0006c0006t0001g0327 a0006c0006t0001g0328 a0006c0006t0001g0329 others(4): Show |
7 | HG01257.hp1 HG01515.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.256+447A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978710 | |||||||
chr9:26978753 | T | C | 4 | a0002c0002t0002g0030 a0002c0002t0002g0045 a0002c0002t0002g0046 others(1): Show |
4 | HG00597.hp1 HG02040.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+490T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978753 | |||||||
chr9:26978953 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.256+690A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978953 | |||||||
chr9:26978964 | C | G | 1 | a0001c0001t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.256+701C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978964 | |||||||
chr9:26978988 | G | A | 20 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.256+725G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978988 | |||||||
chr9:26979029 | C | T | 109 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.256+766C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979029 | |||||||
chr9:26979063 | A | C | 2 | a0002c0002t0002g0074 a0002c0002t0002g0075 |
2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.256+800A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979063 | |||||||
chr9:26979145 | A | G | 1 | a0003c0003t0002g0101 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.256+882A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979145 | |||||||
chr9:26979148 | T | C | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.256+885T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979148 | |||||||
chr9:26979151 | ATT | A | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.256+899_256+900del others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979151 | ||||||
chr9:26979362 | G | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.256+1099G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979362 | |||||||
chr9:26979479 | T | C | 20 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.257-1092T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979479 | |||||||
chr9:26979521 | C | G | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.257-1050C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979521 | |||||||
chr9:26979580 | A | G | 1 | a0002c0002t0002g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.257-991A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979580 | |||||||
chr9:26979703 | C | CT | 61 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(58): Show |
61 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.257-841dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | ||||||
chr9:26979703 | C | CTT | 84 | a0001c0001t0001g0109 a0001c0001t0015g0131 a0001c0001t0018g0128 others(81): Show |
84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.257-842_257-841dup others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | ||||||
chr9:26979703 | C | CTTT | 10 | a0001c0001t0015g0132 a0002c0002t0002g0012 a0002c0002t0002g0069 others(7): Show |
10 | HG01255.hp2 HG01346.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.257-843_257-841dup others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | ||||||
chr9:26979703 | CT | C | 11 | a0001c0001t0001g0151 a0001c0001t0001g0180 a0001c0001t0001g0181 others(8): Show |
11 | HG00099.hp1 HG01074.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.257-841delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | ||||||
chr9:26979703 | CTTTTTTT others(5): Show |
C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.257-852_257-841del others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | ||||||
chr9:26979733 | G | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0200 |
3 | HG02135.hp1 NA19007.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.257-838G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979733 | |||||||
chr9:26979751 | C | T | 1 | a0002c0002t0002g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.257-820C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979751 | |||||||
chr9:26979811 | C | G | 1 | a0001c0001t0003g0282 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.257-760C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979811 | |||||||
chr9:26979896 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.257-675G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979896 | |||||||
chr9:26980004 | C | T | 4 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.257-567C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980004 | |||||||
chr9:26980005 | G | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.257-566G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980005 | |||||||
chr9:26980068 | T | C | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.257-503T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980068 | |||||||
chr9:26980182 | A | G | 31 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(28): Show |
31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.257-389A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980182 | |||||||
chr9:26980187 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.257-384T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980187 | |||||||
chr9:26980281 | C | G | 13 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.257-290C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980281 | |||||||
chr9:26980370 | G | A | 1 | a0007c0007t0006g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.257-201G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980370 | |||||||
chr9:26980415 | A | G | 20 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.257-156A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980415 | |||||||
chr9:26980457 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.257-114G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980457 | |||||||
chr9:26980568 | T | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.257-3T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980568 | |||||||
chr9:26980645 | G | A | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305+26G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980645 | |||||||
chr9:26980802 | G | T | 1 | a0009c0014t0003g0292 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.305+183G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980802 | |||||||
chr9:26980839 | A | T | 1 | a0006c0006t0001g0331 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.305+220A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980839 | |||||||
chr9:26980881 | C | T | 36 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.305+262C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980881 | |||||||
chr9:26980951 | C | T | 20 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.305+332C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980951 | |||||||
chr9:26980958 | C | T | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+339C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980958 | |||||||
chr9:26981029 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.305+410G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981029 | |||||||
chr9:26981117 | C | T | 20 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.305+498C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981117 | |||||||
chr9:26981377 | G | A | 13 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(10): Show |
13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.305+758G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981377 | |||||||
chr9:26981566 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.305+947C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981566 | |||||||
chr9:26981600 | A | G | 13 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.305+981A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981600 | |||||||
chr9:26981768 | A | AT | 13 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0167 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.305+1166dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26981768 | ||||||
chr9:26981768 | AT | A | 8 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0200 others(5): Show |
8 | HG01070.hp2 HG01358.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+1166delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26981768 | ||||||
chr9:26981814 | C | T | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.305+1195C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981814 | |||||||
chr9:26981863 | G | T | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.305+1244G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981863 | |||||||
chr9:26982084 | GT | G | 16 | a0001c0001t0018g0128 a0006c0006t0001g0324 a0006c0006t0001g0325 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.305+1473delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982084 | ||||||
chr9:26982181 | T | TA | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+1562_305+1563i others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982181 | |||||||
chr9:26982182 | G | C | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+1563G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982182 | |||||||
chr9:26982272 | CT | C | 306 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(303): Show |
307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.305+1663delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982272 | ||||||
chr9:26982287 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.305+1668C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982287 | |||||||
chr9:26982288 | G | A | 1 | a0004c0004t0004g0020 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.305+1669G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982288 | |||||||
chr9:26982451 | A | AT | 55 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.306-1784dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | ||||||
chr9:26982451 | A | ATT | 10 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0201 others(7): Show |
10 | HG01123.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.306-1785_306-1784d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | ||||||
chr9:26982451 | AT | A | 23 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(20): Show |
23 | HG00323.hp2 HG01167.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.306-1784delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | ||||||
chr9:26982451 | ATTTTTTT | A | 6 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
6 | NA18944.hp2 NA18966.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.306-1790_306-1784d others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | ||||||
chr9:26982541 | C | T | 1 | a0003c0003t0002g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.306-1716C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982541 | |||||||
chr9:26982871 | C | T | 13 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.306-1386C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982871 | |||||||
chr9:26982881 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.306-1376C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982881 | |||||||
chr9:26982968 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.306-1289C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982968 | |||||||
chr9:26982975 | G | T | 1 | a0006c0006t0001g0331 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.306-1282G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982975 | |||||||
chr9:26983275 | G | A | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.306-982G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983275 | |||||||
chr9:26983303 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.306-954T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983303 | |||||||
chr9:26983440 | A | G | 31 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(28): Show |
31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.306-817A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983440 | |||||||
chr9:26983562 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.306-695C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983562 | |||||||
chr9:26983573 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.306-684A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983573 | |||||||
chr9:26983610 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.306-647A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983610 | |||||||
chr9:26983776 | C | CT | 12 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0255 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.306-458dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26983776 | ||||||
chr9:26983776 | CT | C | 13 | a0001c0001t0001g0139 a0001c0001t0001g0155 a0001c0001t0001g0211 others(10): Show |
13 | HG00099.hp2 HG00558.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.306-458delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26983776 | ||||||
chr9:26983799 | T | C | 1 | a0007c0007t0006g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.306-458T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983799 | |||||||
chr9:26983841 | T | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.306-416T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983841 | |||||||
chr9:26983975 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.306-282G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983975 | |||||||
chr9:26984024 | T | G | 1 | a0001c0001t0003g0295 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.306-233T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26984024 | |||||||
chr9:26984029 | C | A | 1 | a0002c0002t0002g0051 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.306-228C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26984029 | |||||||
chr9:26984172 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.306-85C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26984172 | |||||||
chr9:26984426 | T | A | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+71T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/19 | chr9 | 26984426 | |||||||
chr9:26984496 | C | T | 5 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(2): Show |
5 | HG02056.hp2 NA18960.hp2 NA18973.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.405-3C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/19 | chr9 | 26984496 | |||||||
chr9:26984693 | A | C | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+134A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26984693 | |||||||
chr9:26984745 | A | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG00099.hp2 HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.465+186A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26984745 | |||||||
chr9:26985063 | C | G | 1 | a0001c0001t0001g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.465+504C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985063 | |||||||
chr9:26985341 | G | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.465+782G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985341 | |||||||
chr9:26985486 | A | T | 8 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+927A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985486 | |||||||
chr9:26985588 | T | C | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.465+1029T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985588 | |||||||
chr9:26985729 | T | A | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.465+1170T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985729 | |||||||
chr9:26985795 | AAC | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.465+1240_465+1241d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 26985795 | ||||||
chr9:26985799 | C | T | 1 | a0001c0001t0025g0177 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.465+1240C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985799 | |||||||
chr9:26985852 | A | G | 2 | a0003c0003t0021g0100 a0003c0003t0027g0099 |
2 | NA19077.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.465+1293A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985852 | |||||||
chr9:26985927 | T | C | 13 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(10): Show |
13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.465+1368T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985927 | |||||||
chr9:26986046 | T | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.465+1487T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986046 | |||||||
chr9:26986152 | GAAAT | G | 35 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.465+1597_465+1600d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 26986152 | ||||||
chr9:26986320 | G | T | 3 | a0001c0008t0001g0169 a0001c0008t0001g0170 a0001c0008t0001g0171 |
3 | HG01192.hp2 HG01358.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.465+1761G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986320 | |||||||
chr9:26986380 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.465+1821A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986380 | |||||||
chr9:26986510 | T | C | 93 | a0001c0001t0001g0204 a0001c0001t0001g0246 a0001c0001t0001g0262 others(90): Show |
93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.465+1951T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986510 | |||||||
chr9:26986544 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.465+1985T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986544 | |||||||
chr9:26986561 | C | A | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.465+2002C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986561 | |||||||
chr9:26986649 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.466-2020G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986649 | |||||||
chr9:26986776 | G | C | 24 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(21): Show |
24 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.466-1893G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986776 | |||||||
chr9:26986839 | T | G | 2 | a0001c0001t0015g0131 a0001c0001t0015g0132 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.466-1830T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986839 | |||||||
chr9:26986856 | C | G | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.466-1813C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986856 | |||||||
chr9:26986885 | A | G | 13 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(10): Show |
13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.466-1784A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986885 | |||||||
chr9:26986954 | C | G | 2 | a0001c0001t0015g0131 a0001c0001t0015g0132 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.466-1715C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986954 | |||||||
chr9:26986974 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.466-1695G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986974 | |||||||
chr9:26986979 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0246 a0001c0001t0001g0262 others(1): Show |
4 | HG00609.hp2 NA18975.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1690G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986979 | |||||||
chr9:26987029 | G | A | 167 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(164): Show |
167 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.466-1640G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987029 | |||||||
chr9:26987081 | G | T | 93 | a0001c0001t0001g0204 a0001c0001t0001g0246 a0001c0001t0001g0262 others(90): Show |
93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.466-1588G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987081 | |||||||
chr9:26987132 | C | A | 3 | a0001c0001t0018g0128 a0007c0007t0019g0119 a0011c0010t0017g0115 |
3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.466-1537C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987132 | |||||||
chr9:26987209 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.466-1460G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987209 | |||||||
chr9:26987260 | A | T | 113 | a0001c0001t0001g0204 a0001c0001t0001g0246 a0001c0001t0001g0262 others(110): Show |
113 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.466-1409A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987260 | |||||||
chr9:26987312 | A | G | 113 | a0001c0001t0001g0204 a0001c0001t0001g0246 a0001c0001t0001g0262 others(110): Show |
113 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.466-1357A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987312 | |||||||
chr9:26987382 | G | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.466-1287G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987382 | |||||||
chr9:26987385 | C | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.466-1284C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987385 | |||||||
chr9:26987454 | A | G | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.466-1215A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987454 | |||||||
chr9:26987471 | A | G | 1 | a0001c0001t0010g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.466-1198A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987471 | |||||||
chr9:26987495 | T | G | 31 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(28): Show |
31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.466-1174T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987495 | |||||||
chr9:26987688 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466-981C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987688 | |||||||
chr9:26987772 | G | A | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.466-897G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987772 | |||||||
chr9:26987877 | AT | A | 17 | a0001c0001t0001g0154 a0001c0001t0001g0178 a0001c0001t0001g0181 others(14): Show |
17 | HG00597.hp2 HG02129.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.466-783delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 26987877 | ||||||
chr9:26988055 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0034g0141 |
3 | HG01099.hp2 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.466-614C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988055 | |||||||
chr9:26988087 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG00099.hp2 HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.466-582G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988087 | |||||||
chr9:26988247 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.466-422C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988247 | |||||||
chr9:26988324 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.466-345T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988324 | |||||||
chr9:26988568 | T | G | 2 | a0001c0001t0011g0033 a0001c0001t0011g0036 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.466-101T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988568 | |||||||
chr9:26988573 | A | G | 115 | a0001c0001t0001g0204 a0001c0001t0001g0246 a0001c0001t0001g0262 others(112): Show |
115 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.466-96A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988573 | |||||||
chr9:26988618 | T | A | 6 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0007c0007t0008g0004 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-51T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988618 | |||||||
chr9:26988785 | G | A | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+57G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26988785 | |||||||
chr9:26988785 | G | T | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.525+57G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26988785 | |||||||
chr9:26988860 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.525+132C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26988860 | |||||||
chr9:26989187 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525+459G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989187 | |||||||
chr9:26989242 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0181 a0001c0001t0001g0187 |
3 | NA18964.hp2 NA18967.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.525+514A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989242 | |||||||
chr9:26989385 | G | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+657G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989385 | |||||||
chr9:26989511 | G | A | 1 | a0002c0002t0002g0051 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.526-623G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989511 | |||||||
chr9:26989754 | A | C | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.526-380A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989754 | |||||||
chr9:26989766 | A | C | 1 | a0002c0002t0002g0013 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.526-368A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989766 | |||||||
chr9:26989817 | CA | C | 31 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(28): Show |
31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.526-314delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr9 | 26989817 | ||||||
chr9:26989954 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.526-180T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989954 | |||||||
chr9:26989984 | G | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-150G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989984 | |||||||
chr9:26990048 | A | G | 3 | a0006c0006t0001g0325 a0006c0006t0001g0326 a0006c0006t0026g0207 |
3 | HG02055.hp2 HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526-86A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26990048 | |||||||
chr9:26990083 | A | T | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.526-51A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26990083 | |||||||
chr9:26990364 | T | G | 16 | a0002c0002t0002g0052 a0002c0002t0002g0077 a0002c0002t0002g0078 others(13): Show |
16 | HG00558.hp2 HG00609.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.587+169T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990364 | |||||||
chr9:26990388 | AT | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0188 a0001c0001t0001g0197 others(1): Show |
4 | HG01074.hp1 HG01175.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+194delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990388 | |||||||
chr9:26990394 | A | G | 4 | a0001c0001t0001g0151 a0001c0001t0001g0188 a0001c0001t0001g0197 others(1): Show |
4 | HG01074.hp1 HG01175.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+199A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990394 | |||||||
chr9:26990444 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+249A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990444 | |||||||
chr9:26990486 | G | T | 1 | a0003c0003t0002g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.587+291G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990486 | |||||||
chr9:26990661 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.587+466A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990661 | |||||||
chr9:26990686 | G | A | 3 | a0004c0004t0004g0020 a0004c0004t0004g0021 a0004c0004t0036g0029 |
3 | HG00323.hp2 HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.587+491G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990686 | |||||||
chr9:26990828 | A | T | 12 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(9): Show |
12 | HG00639.hp2 HG01256.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.587+633A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990828 | |||||||
chr9:26990914 | T | G | 1 | a0004c0004t0004g0020 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.587+719T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990914 | |||||||
chr9:26990970 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+775A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990970 | |||||||
chr9:26991207 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG03041.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.587+1012T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991207 | |||||||
chr9:26991329 | T | C | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+1134T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991329 | |||||||
chr9:26991379 | C | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG00099.hp2 HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.587+1184C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991379 | |||||||
chr9:26991409 | A | G | 163 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(160): Show |
163 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.587+1214A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991409 | |||||||
chr9:26991430 | G | A | 1 | a0002c0002t0002g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.587+1235G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991430 | |||||||
chr9:26991475 | C | T | 1 | a0002c0002t0002g0066 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.587+1280C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991475 | |||||||
chr9:26991516 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.587+1321G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991516 | |||||||
chr9:26991796 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+1601C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991796 | |||||||
chr9:26991801 | C | T | 2 | a0001c0001t0001g0117 a0003c0003t0002g0127 |
2 | HG00408.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.587+1606C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991801 | |||||||
chr9:26991832 | C | G | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.587+1637C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991832 | |||||||
chr9:26991832 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.587+1637C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991832 | |||||||
chr9:26991854 | C | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+1659C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991854 | |||||||
chr9:26991914 | A | G | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.587+1719A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991914 | |||||||
chr9:26991946 | T | C | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.587+1751T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991946 | |||||||
chr9:26991984 | G | A | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.587+1789G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991984 | |||||||
chr9:26992035 | C | CA | 86 | a0001c0001t0001g0182 a0001c0001t0018g0128 a0002c0002t0002g0007 others(83): Show |
86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.587+1852dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26992035 | ||||||
chr9:26992047 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587+1852A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992047 | |||||||
chr9:26992140 | A | G | 2 | a0001c0001t0010g0034 a0001c0001t0010g0035 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.587+1945A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992140 | |||||||
chr9:26992508 | T | C | 165 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(162): Show |
166 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.587+2313T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992508 | |||||||
chr9:26992598 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+2403C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992598 | |||||||
chr9:26992635 | G | T | 1 | a0006c0006t0001g0326 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.587+2440G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992635 | |||||||
chr9:26992649 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.587+2454C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992649 | |||||||
chr9:26992658 | A | G | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+2463A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992658 | |||||||
chr9:26992679 | C | T | 12 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(9): Show |
12 | HG00639.hp2 HG01256.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.587+2484C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992679 | |||||||
chr9:26992687 | T | C | 8 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+2492T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992687 | |||||||
chr9:26992692 | C | CA | 12 | a0001c0001t0001g0104 a0001c0001t0001g0264 a0001c0001t0001g0265 others(9): Show |
12 | HG00408.hp2 HG00558.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.587+2510dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26992692 | ||||||
chr9:26992788 | G | A | 1 | a0002c0002t0024g0319 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.587+2593G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992788 | |||||||
chr9:26992860 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0262 |
2 | NA18975.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.587+2665G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992860 | |||||||
chr9:26993030 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.587+2835A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993030 | |||||||
chr9:26993483 | G | A | 1 | a0002c0002t0002g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.587+3288G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993483 | |||||||
chr9:26993595 | A | G | 104 | a0001c0001t0018g0128 a0002c0002t0002g0007 a0002c0002t0002g0008 others(101): Show |
104 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.587+3400A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993595 | |||||||
chr9:26993642 | A | G | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.587+3447A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993642 | |||||||
chr9:26993757 | T | G | 81 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(78): Show |
81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.587+3562T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993757 | |||||||
chr9:26993796 | A | G | 13 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.587+3601A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993796 | |||||||
chr9:26993891 | T | C | 88 | a0001c0001t0018g0128 a0002c0002t0002g0007 a0002c0002t0002g0008 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.587+3696T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993891 | |||||||
chr9:26994223 | A | T | 81 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(78): Show |
81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.587+4028A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994223 | |||||||
chr9:26994331 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+4136G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994331 | |||||||
chr9:26994331 | G | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+4136G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994331 | |||||||
chr9:26994382 | C | T | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.587+4187C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994382 | |||||||
chr9:26994469 | G | A | 1 | a0003c0003t0002g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.587+4274G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994469 | |||||||
chr9:26994493 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0306 |
2 | HG00609.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.587+4298C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994493 | |||||||
chr9:26994536 | C | CA | 18 | a0001c0001t0001g0108 a0001c0001t0001g0133 a0001c0001t0001g0167 others(15): Show |
18 | HG01123.hp2 HG01255.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.587+4361dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26994536 | ||||||
chr9:26994536 | CA | C | 8 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0209 others(5): Show |
8 | HG00099.hp2 HG03209.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+4361delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26994536 | ||||||
chr9:26994600 | C | A | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+4405C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994600 | |||||||
chr9:26994800 | G | A | 330 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(327): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.587+4605G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994800 | |||||||
chr9:26994856 | G | A | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.587+4661G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994856 | |||||||
chr9:26994868 | T | G | 2 | a0001c0001t0011g0033 a0001c0001t0011g0036 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.587+4673T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994868 | |||||||
chr9:26994932 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.587+4737T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994932 | |||||||
chr9:26994971 | A | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+4776A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994971 | |||||||
chr9:26995155 | A | G | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.587+4960A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995155 | |||||||
chr9:26995249 | T | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+5054T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995249 | |||||||
chr9:26995789 | G | A | 16 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.587+5594G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995789 | |||||||
chr9:26995888 | T | C | 17 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.587+5693T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995888 | |||||||
chr9:26995903 | A | G | 1 | a0001c0008t0001g0171 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.587+5708A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995903 | |||||||
chr9:26995929 | C | T | 17 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.587+5734C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995929 | |||||||
chr9:26996172 | G | C | 150 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(147): Show |
150 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.587+5977G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996172 | |||||||
chr9:26996432 | A | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+6237A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996432 | |||||||
chr9:26996478 | C | T | 1 | a0002c0002t0002g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.587+6283C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996478 | |||||||
chr9:26996608 | T | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+6413T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996608 | |||||||
chr9:26996627 | T | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+6432T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996627 | |||||||
chr9:26996720 | A | G | 1 | a0001c0001t0014g0001 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.587+6525A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996720 | |||||||
chr9:26996721 | T | C | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.587+6526T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996721 | |||||||
chr9:26996770 | A | T | 87 | a0001c0001t0018g0128 a0002c0002t0002g0007 a0002c0002t0002g0008 others(84): Show |
87 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.587+6575A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996770 | |||||||
chr9:26996939 | A | G | 8 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+6744A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996939 | |||||||
chr9:26996980 | G | T | 13 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(10): Show |
13 | HG01192.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.587+6785G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996980 | |||||||
chr9:26997056 | C | G | 87 | a0001c0001t0018g0128 a0002c0002t0002g0007 a0002c0002t0002g0008 others(84): Show |
87 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.587+6861C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997056 | |||||||
chr9:26997168 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.587+6973C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997168 | |||||||
chr9:26997209 | T | C | 1 | a0005c0005t0005g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.587+7014T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997209 | |||||||
chr9:26997212 | CA | C | 125 | a0001c0001t0001g0190 a0001c0001t0018g0128 a0002c0002t0002g0007 others(122): Show |
125 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.587+7031delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997212 | ||||||
chr9:26997234 | A | AT | 9 | a0002c0002t0002g0011 a0003c0003t0002g0039 a0003c0003t0002g0089 others(6): Show |
9 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.587+7044dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997234 | ||||||
chr9:26997256 | A | G | 1 | a0005c0005t0005g0311 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+7061A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997256 | |||||||
chr9:26997257 | AGGAGAGC others(3): Show |
A | 1 | a0005c0005t0005g0311 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+7063_587+7072d others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997257 | |||||||
chr9:26997268 | T | A | 1 | a0005c0005t0005g0311 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+7073T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997268 | |||||||
chr9:26997330 | C | CT | 83 | a0001c0001t0001g0178 a0001c0001t0001g0182 a0001c0001t0001g0195 others(80): Show |
84 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.587+7156dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997330 | ||||||
chr9:26997330 | C | CTT | 6 | a0002c0002t0002g0007 a0002c0002t0002g0065 a0002c0002t0002g0069 others(3): Show |
6 | NA18959.hp1 NA18967.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.587+7155_587+7156d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997330 | ||||||
chr9:26997330 | CTTTT | C | 7 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+7153_587+7156d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997330 | ||||||
chr9:26997375 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+7180C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997375 | |||||||
chr9:26997396 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.587+7201C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997396 | |||||||
chr9:26997414 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+7219A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997414 | |||||||
chr9:26997415 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+7220C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997415 | |||||||
chr9:26997444 | C | G | 1 | a0007c0007t0008g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.587+7249C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997444 | |||||||
chr9:26997445 | C | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+7250C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997445 | |||||||
chr9:26997458 | T | C | 8 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+7263T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997458 | |||||||
chr9:26997554 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+7359A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997554 | |||||||
chr9:26997558 | T | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+7363T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997558 | |||||||
chr9:26997606 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587+7411T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997606 | |||||||
chr9:26997626 | G | A | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.587+7431G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997626 | |||||||
chr9:26997982 | T | C | 1 | a0001c0008t0001g0170 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.587+7787T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997982 | |||||||
chr9:26998049 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587+7854C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998049 | |||||||
chr9:26998092 | C | T | 5 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0252 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+7897C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998092 | |||||||
chr9:26998191 | A | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 |
3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.587+7996A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998191 | |||||||
chr9:26998251 | C | T | 8 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+8056C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998251 | |||||||
chr9:26998325 | A | C | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8130A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998325 | |||||||
chr9:26998335 | C | T | 13 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.587+8140C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998335 | |||||||
chr9:26998347 | A | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+8152A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998347 | |||||||
chr9:26998535 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587+8340C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998535 | |||||||
chr9:26998555 | G | A | 304 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(301): Show |
305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.587+8360G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998555 | |||||||
chr9:26998777 | A | T | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.587+8582A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998777 | |||||||
chr9:26998817 | C | T | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.587+8622C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998817 | |||||||
chr9:26998829 | C | CA | 6 | a0001c0001t0001g0165 a0001c0001t0015g0132 a0002c0002t0002g0077 others(3): Show |
6 | HG00558.hp2 HG02738.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.587+8648dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26998829 | ||||||
chr9:26998829 | CAA | C | 8 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+8647_587+8648d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26998829 | ||||||
chr9:26998835 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8640A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998835 | |||||||
chr9:26998850 | C | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8655C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998850 | |||||||
chr9:26998851 | G | A | 30 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 others(27): Show |
31 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.587+8656G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998851 | |||||||
chr9:26998851 | G | C | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8656G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998851 | |||||||
chr9:26999011 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+8816C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999011 | |||||||
chr9:26999013 | A | T | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.587+8818A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999013 | |||||||
chr9:26999116 | G | A | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+8921G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999116 | |||||||
chr9:26999168 | A | ATATAATT others(11): Show |
1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8977_587+8978i others(20): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999168 | ||||||
chr9:26999185 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587+8990G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999185 | |||||||
chr9:26999770 | C | CT | 152 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0107 others(149): Show |
152 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.588-9229dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999770 | ||||||
chr9:26999770 | C | CTT | 16 | a0001c0001t0001g0238 a0001c0001t0001g0252 a0001c0001t0001g0253 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.588-9230_588-9229d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999770 | ||||||
chr9:26999770 | CT | C | 17 | a0001c0001t0001g0183 a0001c0001t0001g0242 a0001c0001t0001g0264 others(14): Show |
17 | HG00408.hp2 HG00558.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.588-9229delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999770 | ||||||
chr9:26999833 | A | G | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-9187A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999833 | |||||||
chr9:26999842 | G | A | 98 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0204 others(95): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.588-9178G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999842 | |||||||
chr9:26999920 | A | C | 1 | a0002c0002t0002g0064 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.588-9100A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999920 | |||||||
chr9:27000238 | G | A | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.588-8782G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000238 | |||||||
chr9:27000342 | C | T | 163 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(160): Show |
163 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.588-8678C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000342 | |||||||
chr9:27000500 | A | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-8520A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000500 | |||||||
chr9:27000746 | G | A | 2 | a0003c0003t0002g0043 a0003c0003t0002g0050 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588-8274G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000746 | |||||||
chr9:27000766 | C | T | 1 | a0001c0001t0003g0299 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.588-8254C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000766 | |||||||
chr9:27000849 | A | G | 14 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.588-8171A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000849 | |||||||
chr9:27001109 | G | A | 1 | a0010c0013t0031g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.588-7911G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001109 | |||||||
chr9:27001135 | T | G | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-7885T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001135 | |||||||
chr9:27001191 | T | A | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.588-7829T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001191 | |||||||
chr9:27001215 | A | C | 4 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-7805A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001215 | |||||||
chr9:27001238 | G | A | 1 | a0001c0012t0003g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.588-7782G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001238 | |||||||
chr9:27001380 | CT | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-7638delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001380 | ||||||
chr9:27001588 | G | GT | 17 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-7429dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001588 | ||||||
chr9:27001601 | G | T | 1 | a0002c0002t0002g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.588-7419G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001601 | |||||||
chr9:27001602 | T | A | 1 | a0002c0002t0002g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.588-7418T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001602 | |||||||
chr9:27001603 | G | A | 1 | a0002c0002t0002g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.588-7417G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001603 | |||||||
chr9:27001647 | G | A | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.588-7373G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001647 | |||||||
chr9:27001942 | C | CT | 41 | a0001c0001t0001g0240 a0001c0001t0001g0287 a0001c0001t0001g0290 others(38): Show |
42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.588-7066dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001942 | ||||||
chr9:27001942 | CT | C | 14 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0168 others(11): Show |
14 | HG01515.hp2 HG01891.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-7066delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001942 | ||||||
chr9:27002004 | T | A | 330 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(327): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.588-7016T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002004 | |||||||
chr9:27002009 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.588-7011G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002009 | |||||||
chr9:27002013 | G | T | 4 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-7007G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002013 | |||||||
chr9:27002026 | G | A | 1 | a0009c0014t0003g0292 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.588-6994G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002026 | |||||||
chr9:27002196 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.588-6824A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002196 | |||||||
chr9:27002319 | C | G | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-6701C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002319 | |||||||
chr9:27002367 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.588-6653G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002367 | |||||||
chr9:27002378 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.588-6642G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002378 | |||||||
chr9:27002514 | G | C | 25 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(22): Show |
25 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.588-6506G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002514 | |||||||
chr9:27002568 | C | A | 13 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(10): Show |
13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.588-6452C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002568 | |||||||
chr9:27002612 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.588-6408T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002612 | |||||||
chr9:27002613 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.588-6407A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002613 | |||||||
chr9:27002782 | T | C | 17 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-6238T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002782 | |||||||
chr9:27002828 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588-6192G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002828 | |||||||
chr9:27002830 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0200 others(1): Show |
4 | HG02135.hp1 HG03209.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-6190G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002830 | |||||||
chr9:27003205 | G | GT | 18 | a0002c0002t0002g0085 a0004c0004t0004g0014 a0004c0004t0004g0015 others(15): Show |
18 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-5805dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27003205 | ||||||
chr9:27003277 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-5743C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003277 | |||||||
chr9:27003352 | A | C | 3 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 |
3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.588-5668A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003352 | |||||||
chr9:27003388 | T | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-5632T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003388 | |||||||
chr9:27003514 | C | G | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.588-5506C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003514 | |||||||
chr9:27003554 | G | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-5466G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003554 | |||||||
chr9:27003557 | A | G | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-5463A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003557 | |||||||
chr9:27003849 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.588-5171G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003849 | |||||||
chr9:27003899 | T | C | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-5121T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003899 | |||||||
chr9:27003919 | C | T | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-5101C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003919 | |||||||
chr9:27003994 | G | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-5026G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003994 | |||||||
chr9:27004198 | A | C | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG01069.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.588-4822A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004198 | |||||||
chr9:27004312 | CTTGGAAG others(57): Show |
C | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-4707_588-4644d others(66): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004312 | |||||||
chr9:27004340 | G | A | 34 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(31): Show |
34 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.588-4680G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004340 | |||||||
chr9:27004379 | A | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-4641A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004379 | |||||||
chr9:27005022 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-3998A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005022 | |||||||
chr9:27005064 | A | G | 92 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(89): Show |
92 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.588-3956A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005064 | |||||||
chr9:27005066 | G | A | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(24): Show |
27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.588-3954G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005066 | |||||||
chr9:27005130 | A | AT | 4 | a0002c0002t0002g0069 a0007c0007t0008g0004 a0007c0007t0008g0005 others(1): Show |
4 | HG02615.hp1 HG03579.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-3883dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005130 | ||||||
chr9:27005229 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.588-3791A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005229 | |||||||
chr9:27005296 | T | C | 2 | a0001c0001t0013g0266 a0001c0001t0013g0267 |
2 | NA18959.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.588-3724T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005296 | |||||||
chr9:27005351 | T | TC | 3 | a0001c0001t0001g0154 a0001c0001t0001g0210 a0001c0001t0032g0225 |
3 | NA18612.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.588-3669_588-3668i others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005351 | |||||||
chr9:27005352 | T | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0178 a0001c0001t0001g0181 others(6): Show |
9 | HG00597.hp2 HG00741.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-3668T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005352 | |||||||
chr9:27005352 | T | TC | 74 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0133 others(71): Show |
75 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.588-3660dupC | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCC | 17 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0156 others(14): Show |
17 | HG01074.hp2 HG01175.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.588-3661_588-3660d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCACCCC others(7): Show |
2 | a0003c0003t0002g0321 a0003c0003t0002g0322 |
2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.588-3666_588-3665i others(16): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCACCCC others(9): Show |
1 | a0003c0003t0002g0323 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.588-3666_588-3665i others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCACCCC others(10): Show |
1 | a0003c0003t0002g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.588-3666_588-3665i others(19): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCCCCG | 25 | a0001c0001t0001g0251 a0001c0001t0001g0256 a0002c0002t0002g0011 others(22): Show |
25 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.588-3663_588-3662i others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCCCCGC | 23 | a0002c0002t0002g0007 a0002c0002t0002g0009 a0002c0002t0002g0010 others(20): Show |
23 | HG00597.hp1 HG01346.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.588-3663_588-3662i others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCCCCGC others(1): Show |
18 | a0001c0001t0001g0231 a0001c0001t0001g0253 a0002c0002t0002g0008 others(15): Show |
18 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-3663_588-3662i others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCCCCGC others(3): Show |
2 | a0002c0002t0002g0048 a0002c0002t0002g0057 |
2 | HG01255.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.588-3663_588-3662i others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCCCCGC others(4): Show |
2 | a0002c0002t0002g0085 a0002c0002t0002g0126 |
2 | HG02135.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.588-3663_588-3662i others(13): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005352 | T | TCCCCCGC others(6): Show |
1 | a0002c0002t0002g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.588-3663_588-3662i others(15): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | ||||||
chr9:27005355 | C | G | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(3): Show |
6 | HG00423.hp1 HG02080.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.588-3665C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005355 | |||||||
chr9:27005357 | C | G | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-3663C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005357 | |||||||
chr9:27005360 | CG | C | 52 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(49): Show |
52 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.588-3659delG | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005360 | |||||||
chr9:27005361 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0028g0300 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.588-3659G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005361 | |||||||
chr9:27005361 | G | C | 265 | a0001c0001t0001g0104 a0001c0001t0001g0116 a0001c0001t0001g0118 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.588-3659G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005361 | |||||||
chr9:27005363 | C | G | 1 | a0001c0001t0003g0283 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.588-3657C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005363 | |||||||
chr9:27005429 | T | C | 8 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-3591T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005429 | |||||||
chr9:27005454 | G | C | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.588-3566G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005454 | |||||||
chr9:27005489 | T | C | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-3531T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005489 | |||||||
chr9:27005545 | TA | T | 5 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0007c0007t0006g0017 others(2): Show |
5 | HG00733.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-3467delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005545 | ||||||
chr9:27005546 | A | T | 4 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-3474A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005546 | |||||||
chr9:27005567 | A | G | 32 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(29): Show |
32 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.588-3453A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005567 | |||||||
chr9:27005572 | T | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-3448T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005572 | |||||||
chr9:27005620 | G | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.588-3400G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005620 | |||||||
chr9:27005659 | A | G | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.588-3361A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005659 | |||||||
chr9:27005756 | T | C | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.588-3264T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005756 | |||||||
chr9:27005841 | C | CT | 29 | a0001c0001t0001g0240 a0001c0001t0001g0287 a0001c0001t0001g0290 others(26): Show |
30 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.588-3171dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005841 | ||||||
chr9:27005862 | T | C | 207 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(204): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.588-3158T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005862 | |||||||
chr9:27005944 | G | A | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-3076G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005944 | |||||||
chr9:27006127 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.588-2893A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006127 | |||||||
chr9:27006340 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-2680G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006340 | |||||||
chr9:27006515 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-2505G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006515 | |||||||
chr9:27006550 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588-2470T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006550 | |||||||
chr9:27006577 | A | G | 104 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0204 others(101): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.588-2443A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006577 | |||||||
chr9:27006623 | A | AAG | 17 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-2381_588-2380d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006623 | ||||||
chr9:27006623 | AAGAG | A | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-2383_588-2380d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006623 | ||||||
chr9:27006749 | A | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01496.hp1 HG02615.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.588-2271A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006749 | |||||||
chr9:27006761 | A | C | 3 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0007c0007t0019g0119 |
3 | HG01255.hp2 HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.588-2259A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006761 | |||||||
chr9:27006831 | G | GT | 28 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0116 others(25): Show |
28 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.588-2166dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006831 | ||||||
chr9:27006831 | GT | G | 144 | a0001c0001t0001g0121 a0001c0001t0001g0133 a0001c0001t0001g0134 others(141): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.588-2166delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006831 | ||||||
chr9:27006831 | GTT | G | 7 | a0001c0001t0001g0216 a0001c0001t0001g0244 a0001c0001t0001g0287 others(4): Show |
7 | HG00323.hp1 HG01069.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-2167_588-2166d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006831 | ||||||
chr9:27006859 | T | C | 1 | a0001c0001t0003g0282 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.588-2161T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006859 | |||||||
chr9:27006981 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-2039C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006981 | |||||||
chr9:27007047 | A | C | 1 | a0006c0006t0001g0335 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.588-1973A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007047 | |||||||
chr9:27007084 | G | A | 1 | a0006c0006t0001g0324 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.588-1936G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007084 | |||||||
chr9:27007129 | G | T | 1 | a0007c0007t0008g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.588-1891G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007129 | |||||||
chr9:27007392 | G | A | 3 | a0004c0004t0004g0019 a0004c0004t0004g0023 a0004c0004t0004g0024 |
3 | HG00733.hp2 HG01934.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.588-1628G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007392 | |||||||
chr9:27007639 | A | G | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.588-1381A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007639 | |||||||
chr9:27007856 | G | T | 1 | a0002c0002t0002g0062 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.588-1164G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007856 | |||||||
chr9:27007906 | C | T | 17 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-1114C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007906 | |||||||
chr9:27007923 | G | C | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-1097G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007923 | |||||||
chr9:27007924 | T | C | 2 | a0003c0003t0002g0043 a0003c0003t0002g0050 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588-1096T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007924 | |||||||
chr9:27008314 | A | G | 2 | a0003c0003t0002g0321 a0003c0003t0002g0322 |
2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.588-706A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008314 | |||||||
chr9:27008397 | G | T | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.588-623G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008397 | |||||||
chr9:27008409 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.588-611G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008409 | |||||||
chr9:27008420 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.588-600C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008420 | |||||||
chr9:27008559 | C | T | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.588-461C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008559 | |||||||
chr9:27008645 | C | T | 9 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG01496.hp1 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.588-375C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008645 | |||||||
chr9:27008654 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-366G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008654 | |||||||
chr9:27008666 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.588-354T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008666 | |||||||
chr9:27008818 | TA | T | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-197delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27008818 | ||||||
chr9:27008986 | T | A | 2 | a0001c0001t0010g0034 a0001c0001t0010g0035 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.588-34T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008986 | |||||||
chr9:27009241 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00099.hp1 HG00140.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.726+83C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009241 | |||||||
chr9:27009293 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.726+135C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009293 | |||||||
chr9:27009297 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.726+139C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009297 | |||||||
chr9:27009307 | C | T | 81 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(78): Show |
81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.726+149C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009307 | |||||||
chr9:27009308 | G | A | 1 | a0002c0002t0002g0052 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.726+150G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009308 | |||||||
chr9:27009346 | C | A | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.726+188C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009346 | |||||||
chr9:27009405 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.726+247A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009405 | |||||||
chr9:27009478 | C | T | 5 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(2): Show |
5 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+320C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009478 | |||||||
chr9:27009492 | C | T | 2 | a0005c0005t0005g0310 a0005c0005t0005g0317 |
2 | HG01256.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.726+334C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009492 | |||||||
chr9:27009581 | C | T | 99 | a0001c0001t0018g0128 a0002c0002t0002g0007 a0002c0002t0002g0008 others(96): Show |
99 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.726+423C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009581 | |||||||
chr9:27009658 | C | T | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.726+500C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009658 | |||||||
chr9:27009686 | C | G | 14 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.726+528C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009686 | |||||||
chr9:27009740 | A | C | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.726+582A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009740 | |||||||
chr9:27009853 | A | C | 1 | a0004c0004t0004g0276 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.726+695A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009853 | |||||||
chr9:27009914 | G | A | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.726+756G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009914 | |||||||
chr9:27009971 | AT | A | 17 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(14): Show |
17 | HG00639.hp2 HG01256.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.726+826delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27009971 | ||||||
chr9:27009984 | T | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+826T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009984 | |||||||
chr9:27010081 | G | A | 8 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0247 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+923G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010081 | |||||||
chr9:27010181 | G | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.726+1023G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010181 | |||||||
chr9:27010193 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.726+1035G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010193 | |||||||
chr9:27010208 | C | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.726+1050C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010208 | |||||||
chr9:27010225 | G | A | 8 | a0003c0003t0002g0039 a0003c0003t0002g0089 a0003c0003t0002g0090 others(5): Show |
8 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.726+1067G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010225 | |||||||
chr9:27010280 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+1122C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010280 | |||||||
chr9:27010476 | CTTTTTTT others(7): Show |
C | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.726+1336_726+1349d others(16): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27010476 | ||||||
chr9:27010485 | G | GT | 33 | a0001c0001t0001g0116 a0001c0001t0001g0155 a0001c0001t0001g0163 others(30): Show |
33 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.726+1340dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27010485 | ||||||
chr9:27010496 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.726+1338T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010496 | |||||||
chr9:27010552 | C | T | 2 | a0001c0001t0010g0034 a0001c0001t0010g0035 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.727-1354C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010552 | |||||||
chr9:27010559 | G | T | 1 | a0002c0002t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.727-1347G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010559 | |||||||
chr9:27010684 | T | G | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-1222T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010684 | |||||||
chr9:27010714 | CCCCTCGG others(3): Show |
C | 32 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(29): Show |
32 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.727-1188_727-1179d others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27010714 | ||||||
chr9:27010745 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.727-1161G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010745 | |||||||
chr9:27010783 | A | G | 1 | a0004c0004t0004g0025 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.727-1123A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010783 | |||||||
chr9:27010878 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.727-1028G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010878 | |||||||
chr9:27011042 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.727-864T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011042 | |||||||
chr9:27011168 | G | A | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.727-738G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011168 | |||||||
chr9:27011175 | C | G | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.727-731C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011175 | |||||||
chr9:27011198 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.727-708G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011198 | |||||||
chr9:27011363 | G | T | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-543G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011363 | |||||||
chr9:27011369 | T | A | 93 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(90): Show |
93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.727-537T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011369 | |||||||
chr9:27011387 | C | CGTGTATG others(38): Show |
2 | a0001c0001t0003g0277 a0001c0001t0003g0278 |
2 | HG01175.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.727-504_727-460dup others(45): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011387 | ||||||
chr9:27011396 | A | G | 2 | a0003c0003t0002g0090 a0003c0003t0002g0092 |
2 | NA19010.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.727-510A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011396 | |||||||
chr9:27011642 | GAAGTTTT others(27): Show |
G | 1 | a0001c0001t0003g0295 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.727-255_727-222del others(34): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011642 | ||||||
chr9:27011645 | G | GT | 6 | a0001c0001t0001g0165 a0001c0001t0001g0181 a0001c0001t0001g0221 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-243dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011645 | ||||||
chr9:27011645 | GT | G | 105 | a0001c0001t0001g0143 a0001c0001t0001g0228 a0001c0001t0001g0230 others(102): Show |
105 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.727-243delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011645 | ||||||
chr9:27011645 | GTT | G | 28 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(25): Show |
28 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.727-244_727-243del others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011645 | ||||||
chr9:27011812 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.727-94G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011812 | |||||||
chr9:27011876 | A | G | 1 | a0001c0001t0003g0299 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.727-30A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011876 | |||||||
chr9:27012025 | G | C | 8 | a0003c0003t0002g0039 a0003c0003t0002g0089 a0003c0003t0002g0090 others(5): Show |
8 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+57G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012025 | |||||||
chr9:27012157 | A | T | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+189A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012157 | |||||||
chr9:27012326 | G | A | 3 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0001c0012t0003g0301 |
3 | HG00735.hp1 HG01361.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.789+358G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012326 | |||||||
chr9:27012365 | G | A | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(24): Show |
27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.789+397G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012365 | |||||||
chr9:27012382 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.789+414C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012382 | |||||||
chr9:27012422 | C | T | 5 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+454C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012422 | |||||||
chr9:27012484 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+516C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012484 | |||||||
chr9:27012489 | A | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789+521A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012489 | |||||||
chr9:27012498 | A | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789+530A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012498 | |||||||
chr9:27012510 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.789+542G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012510 | |||||||
chr9:27012649 | C | G | 1 | a0001c0001t0001g0235 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.789+681C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012649 | |||||||
chr9:27012686 | C | G | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+718C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012686 | |||||||
chr9:27012706 | C | CTGTTTT | 8 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0122 others(5): Show |
8 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+740_789+745dup others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012706 | ||||||
chr9:27012708 | G | GT | 14 | a0001c0001t0001g0149 a0001c0001t0001g0155 a0001c0001t0001g0163 others(11): Show |
14 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+767dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | ||||||
chr9:27012708 | G | GTTTTT | 40 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0253 others(37): Show |
40 | HG00558.hp2 HG01081.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.789+763_789+767dup others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | ||||||
chr9:27012708 | G | GTTTTTT | 37 | a0001c0001t0001g0251 a0002c0002t0002g0008 a0002c0002t0002g0011 others(34): Show |
37 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.789+762_789+767dup others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | ||||||
chr9:27012708 | G | GTTTTTTT | 10 | a0002c0002t0002g0042 a0002c0002t0002g0044 a0002c0002t0002g0066 others(7): Show |
10 | HG00408.hp1 HG03710.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+761_789+767dup others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | ||||||
chr9:27012708 | GT | G | 97 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(94): Show |
98 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.789+767delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | ||||||
chr9:27012709 | T | TTTTTG | 23 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(20): Show |
23 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.789+745_789+746ins others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012709 | ||||||
chr9:27012723 | T | G | 3 | a0004c0004t0004g0020 a0004c0004t0004g0276 a0004c0004t0036g0029 |
3 | HG01361.hp2 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.789+755T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012723 | |||||||
chr9:27012747 | C | T | 1 | a0002c0002t0002g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.789+779C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012747 | |||||||
chr9:27012761 | G | A | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+793G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012761 | |||||||
chr9:27012766 | G | T | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+798G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012766 | |||||||
chr9:27012795 | C | A | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.789+827C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012795 | |||||||
chr9:27012938 | C | T | 35 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0138 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.789+970C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012938 | |||||||
chr9:27012947 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+979G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012947 | |||||||
chr9:27012949 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.789+981C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012949 | |||||||
chr9:27013073 | A | C | 1 | a0002c0002t0002g0009 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.789+1105A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013073 | |||||||
chr9:27013077 | G | C | 1 | a0002c0002t0002g0102 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.789+1109G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013077 | |||||||
chr9:27013185 | A | G | 1 | a0001c0001t0028g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.789+1217A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013185 | |||||||
chr9:27013407 | G | A | 1 | a0006c0006t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.789+1439G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013407 | |||||||
chr9:27013426 | G | T | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789+1458G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013426 | |||||||
chr9:27013596 | T | G | 170 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(167): Show |
170 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.789+1628T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013596 | |||||||
chr9:27013627 | A | T | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+1659A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013627 | |||||||
chr9:27013819 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.789+1851G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013819 | |||||||
chr9:27013883 | T | C | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+1915T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013883 | |||||||
chr9:27013963 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.789+1995C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013963 | |||||||
chr9:27013987 | A | G | 2 | a0001c0001t0011g0033 a0001c0001t0011g0036 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.789+2019A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013987 | |||||||
chr9:27014005 | G | C | 1 | a0001c0001t0001g0181 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.789+2037G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014005 | |||||||
chr9:27014006 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.789+2038G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014006 | |||||||
chr9:27014011 | C | T | 14 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+2043C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014011 | |||||||
chr9:27014012 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.789+2044G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014012 | |||||||
chr9:27014013 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.789+2045A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014013 | |||||||
chr9:27014123 | A | G | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2155A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014123 | |||||||
chr9:27014173 | C | T | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2205C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014173 | |||||||
chr9:27014194 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.789+2226G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014194 | |||||||
chr9:27014347 | A | G | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.789+2379A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014347 | |||||||
chr9:27014503 | G | T | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.790-2404G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014503 | |||||||
chr9:27014504 | T | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790-2403T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014504 | |||||||
chr9:27014620 | A | T | 12 | a0002c0002t0002g0059 a0002c0002t0002g0066 a0003c0003t0002g0320 others(9): Show |
12 | HG00621.hp2 HG01255.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.790-2287A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014620 | |||||||
chr9:27014636 | G | C | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-2271G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014636 | |||||||
chr9:27014714 | A | G | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.790-2193A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014714 | |||||||
chr9:27014735 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-2172G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014735 | |||||||
chr9:27014801 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.790-2106G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014801 | |||||||
chr9:27014809 | G | C | 88 | a0001c0001t0002g0289 a0001c0001t0018g0128 a0002c0002t0002g0007 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.790-2098G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014809 | |||||||
chr9:27015029 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.790-1878G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015029 | |||||||
chr9:27015197 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.790-1710A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015197 | |||||||
chr9:27015241 | T | A | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.790-1666T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015241 | |||||||
chr9:27015264 | A | C | 3 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 |
3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.790-1643A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015264 | |||||||
chr9:27015509 | C | T | 1 | a0002c0002t0002g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.790-1398C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015509 | |||||||
chr9:27015605 | C | G | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.790-1302C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015605 | |||||||
chr9:27015727 | T | C | 1 | a0005c0005t0005g0308 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.790-1180T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015727 | |||||||
chr9:27016142 | C | A | 8 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 others(5): Show |
8 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.790-765C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016142 | |||||||
chr9:27016337 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.790-570C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016337 | |||||||
chr9:27016627 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.790-280A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016627 | |||||||
chr9:27016652 | C | G | 14 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.790-255C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016652 | |||||||
chr9:27016808 | G | A | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.790-99G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016808 | |||||||
chr9:27016833 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.790-74A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016833 | |||||||
chr9:27016889 | C | G | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.790-18C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016889 | |||||||
chr9:27017138 | A | G | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.933+88A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017138 | |||||||
chr9:27017210 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.933+160C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017210 | |||||||
chr9:27017266 | A | G | 1 | a0002c0002t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.933+216A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017266 | |||||||
chr9:27017318 | C | G | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+268C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017318 | |||||||
chr9:27017755 | G | A | 2 | a0001c0001t0015g0131 a0001c0001t0015g0132 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.933+705G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017755 | |||||||
chr9:27017961 | G | T | 5 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(2): Show |
5 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-686G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017961 | |||||||
chr9:27018022 | A | G | 171 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(168): Show |
171 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.934-625A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018022 | |||||||
chr9:27018038 | A | G | 15 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG01192.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.934-609A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018038 | |||||||
chr9:27018221 | A | G | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.934-426A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018221 | |||||||
chr9:27018377 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.934-270C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018377 | |||||||
chr9:27018590 | G | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.934-57G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018590 | |||||||
chr9:27018784 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.974+97T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27018784 | |||||||
chr9:27019351 | C | T | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+664C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019351 | |||||||
chr9:27019442 | G | C | 93 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(90): Show |
93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.974+755G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019442 | |||||||
chr9:27019744 | T | G | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(24): Show |
27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.974+1057T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019744 | |||||||
chr9:27019836 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.974+1149G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019836 | |||||||
chr9:27019852 | G | C | 94 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(91): Show |
94 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.974+1165G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019852 | |||||||
chr9:27019873 | A | G | 1 | a0001c0001t0003g0288 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.974+1186A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019873 | |||||||
chr9:27019904 | C | A | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.974+1217C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019904 | |||||||
chr9:27019976 | A | AT | 10 | a0001c0001t0001g0261 a0002c0002t0002g0046 a0002c0002t0002g0069 others(7): Show |
10 | HG00733.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.974+1304dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27019976 | ||||||
chr9:27019994 | G | A | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(24): Show |
27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.974+1307G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019994 | |||||||
chr9:27020007 | A | G | 161 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(158): Show |
161 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.974+1320A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020007 | |||||||
chr9:27020015 | G | A | 1 | a0001c0001t0010g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.974+1328G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020015 | |||||||
chr9:27020064 | A | T | 1 | a0001c0001t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.974+1377A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020064 | |||||||
chr9:27020244 | T | C | 164 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(161): Show |
164 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.974+1557T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020244 | |||||||
chr9:27020255 | A | G | 1 | a0006c0006t0001g0327 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.974+1568A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020255 | |||||||
chr9:27020474 | T | G | 13 | a0001c0001t0001g0238 a0001c0001t0001g0241 a0001c0001t0001g0242 others(10): Show |
13 | HG01257.hp2 HG01258.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.974+1787T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020474 | |||||||
chr9:27020560 | C | T | 5 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0019g0119 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+1873C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020560 | |||||||
chr9:27020561 | T | G | 8 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 others(5): Show |
8 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.974+1874T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020561 | |||||||
chr9:27020826 | G | C | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.974+2139G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020826 | |||||||
chr9:27020862 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.974+2175G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020862 | |||||||
chr9:27021173 | A | G | 3 | a0001c0001t0010g0034 a0001c0001t0011g0033 a0001c0001t0011g0036 |
3 | HG02451.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.974+2486A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021173 | |||||||
chr9:27021239 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.974+2552G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021239 | |||||||
chr9:27021372 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.974+2685T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021372 | |||||||
chr9:27021458 | A | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.974+2771A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021458 | |||||||
chr9:27021550 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.974+2863T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021550 | |||||||
chr9:27021584 | G | A | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.974+2897G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021584 | |||||||
chr9:27021618 | G | A | 1 | a0001c0001t0010g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.974+2931G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021618 | |||||||
chr9:27021770 | A | G | 1 | a0001c0001t0035g0243 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.974+3083A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021770 | |||||||
chr9:27021952 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.974+3265G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021952 | |||||||
chr9:27021995 | A | C | 94 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(91): Show |
94 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.974+3308A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021995 | |||||||
chr9:27021996 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3309T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021996 | |||||||
chr9:27021997 | T | C | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3310T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021997 | |||||||
chr9:27022002 | T | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3315T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022002 | |||||||
chr9:27022003 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3316T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022003 | |||||||
chr9:27022007 | A | G | 27 | a0001c0001t0001g0240 a0001c0001t0003g0002 a0001c0001t0003g0273 others(24): Show |
28 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.974+3320A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022007 | |||||||
chr9:27022008 | T | TCTCTCTC others(25): Show |
1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3321_974+3322i others(34): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022008 | |||||||
chr9:27022021 | G | C | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3334G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022021 | |||||||
chr9:27022022 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3335A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022022 | |||||||
chr9:27022023 | G | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3336G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022023 | |||||||
chr9:27022028 | C | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3341C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022028 | |||||||
chr9:27022029 | A | C | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3342A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022029 | |||||||
chr9:27022032 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3345T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022032 | |||||||
chr9:27022038 | CTCCTACT others(43): Show |
C | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3356_974+3405d others(52): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27022038 | ||||||
chr9:27022061 | A | T | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+3374A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022061 | |||||||
chr9:27022091 | C | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3404C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022091 | |||||||
chr9:27022097 | C | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3410C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022097 | |||||||
chr9:27022099 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3412A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022099 | |||||||
chr9:27022103 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3416T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022103 | |||||||
chr9:27022104 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3417A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022104 | |||||||
chr9:27022109 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3422T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022109 | |||||||
chr9:27022112 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3425T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022112 | |||||||
chr9:27022115 | G | GAGAGAGA others(4): Show |
1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3428_974+3429i others(13): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022115 | |||||||
chr9:27022118 | T | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3431T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022118 | |||||||
chr9:27022119 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3432T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022119 | |||||||
chr9:27022120 | T | A | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3433T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022120 | |||||||
chr9:27022124 | A | G | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3437A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022124 | |||||||
chr9:27022125 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3438A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022125 | |||||||
chr9:27022126 | G | T | 1 | a0002c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3439G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022126 | |||||||
chr9:27022241 | T | C | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.974+3554T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022241 | |||||||
chr9:27022319 | C | T | 25 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(22): Show |
25 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.974+3632C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022319 | |||||||
chr9:27022343 | G | C | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.974+3656G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022343 | |||||||
chr9:27022507 | G | A | 5 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(2): Show |
5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.974+3820G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022507 | |||||||
chr9:27022516 | T | G | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+3829T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022516 | |||||||
chr9:27022646 | C | CT | 127 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0116 others(124): Show |
127 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.974+3973dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27022646 | ||||||
chr9:27022646 | CT | C | 9 | a0001c0001t0001g0259 a0001c0001t0003g0282 a0001c0001t0009g0031 others(6): Show |
9 | HG00140.hp1 HG01255.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.974+3973delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27022646 | ||||||
chr9:27022803 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.974+4116G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022803 | |||||||
chr9:27022887 | C | T | 1 | a0003c0003t0002g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.974+4200C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022887 | |||||||
chr9:27022919 | T | C | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+4232T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022919 | |||||||
chr9:27022938 | G | A | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.974+4251G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022938 | |||||||
chr9:27023006 | A | G | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.974+4319A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023006 | |||||||
chr9:27023110 | A | G | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.974+4423A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023110 | |||||||
chr9:27023265 | C | T | 10 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0006g0017 others(7): Show |
10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.974+4578C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023265 | |||||||
chr9:27023287 | C | T | 2 | a0001c0001t0010g0034 a0001c0001t0010g0035 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.974+4600C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023287 | |||||||
chr9:27023343 | A | G | 1 | a0002c0002t0002g0096 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.974+4656A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023343 | |||||||
chr9:27023560 | A | AT | 13 | a0002c0002t0002g0069 a0006c0006t0001g0324 a0006c0006t0001g0325 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.974+4882dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27023560 | ||||||
chr9:27023581 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.974+4894C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023581 | |||||||
chr9:27023596 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.974+4909G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023596 | |||||||
chr9:27023620 | T | G | 97 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0233 others(94): Show |
97 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.974+4933T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023620 | |||||||
chr9:27023941 | A | T | 1 | a0003c0003t0027g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.975-5084A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023941 | |||||||
chr9:27024179 | A | G | 93 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(90): Show |
93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.975-4846A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024179 | |||||||
chr9:27024347 | G | T | 1 | a0001c0001t0010g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.975-4678G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024347 | |||||||
chr9:27024419 | A | G | 2 | a0001c0001t0011g0033 a0001c0001t0011g0036 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.975-4606A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024419 | |||||||
chr9:27024452 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.975-4573T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024452 | |||||||
chr9:27024517 | A | C | 1 | a0003c0003t0002g0098 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.975-4508A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024517 | |||||||
chr9:27024791 | A | G | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-4234A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024791 | |||||||
chr9:27024974 | T | TA | 10 | a0001c0001t0001g0153 a0001c0001t0009g0031 a0001c0001t0009g0032 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.975-4037dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27024974 | ||||||
chr9:27024974 | T | TAA | 11 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(8): Show |
11 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-4038_975-4037d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27024974 | ||||||
chr9:27024974 | TA | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0155 a0001c0001t0001g0163 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.975-4037delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27024974 | ||||||
chr9:27024989 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0034g0141 |
3 | HG01099.hp2 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.975-4036G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024989 | |||||||
chr9:27025019 | G | A | 7 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(4): Show |
7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.975-4006G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025019 | |||||||
chr9:27025156 | A | G | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.975-3869A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025156 | |||||||
chr9:27025313 | C | T | 1 | a0001c0001t0007g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.975-3712C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025313 | |||||||
chr9:27025423 | A | G | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.975-3602A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025423 | |||||||
chr9:27025429 | T | C | 97 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0001c0001t0018g0128 others(94): Show |
97 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.975-3596T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025429 | |||||||
chr9:27025443 | C | CA | 41 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0167 others(38): Show |
42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.975-3562dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27025443 | ||||||
chr9:27025443 | CA | C | 113 | a0001c0001t0001g0130 a0001c0001t0010g0034 a0001c0001t0010g0035 others(110): Show |
113 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.975-3562delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27025443 | ||||||
chr9:27025443 | CAA | C | 13 | a0002c0002t0002g0048 a0002c0002t0002g0049 a0002c0002t0002g0056 others(10): Show |
13 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.975-3563_975-3562d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27025443 | ||||||
chr9:27025459 | A | G | 6 | a0001c0001t0001g0227 a0001c0001t0009g0031 a0001c0001t0009g0032 others(3): Show |
6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.975-3566A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025459 | |||||||
chr9:27025460 | A | G | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.975-3565A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025460 | |||||||
chr9:27025495 | A | C | 10 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0006g0017 others(7): Show |
10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-3530A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025495 | |||||||
chr9:27025533 | T | C | 1 | a0002c0002t0002g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.975-3492T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025533 | |||||||
chr9:27025691 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.975-3334C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025691 | |||||||
chr9:27025854 | C | T | 7 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(4): Show |
7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.975-3171C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025854 | |||||||
chr9:27025976 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.975-3049A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025976 | |||||||
chr9:27026044 | G | A | 1 | a0005c0005t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.975-2981G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026044 | |||||||
chr9:27026132 | G | C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.975-2893G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026132 | |||||||
chr9:27026144 | T | A | 163 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(160): Show |
163 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.975-2881T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026144 | |||||||
chr9:27026192 | T | C | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.975-2833T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026192 | |||||||
chr9:27026375 | A | G | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-2650A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026375 | |||||||
chr9:27026417 | C | T | 7 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(4): Show |
7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.975-2608C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026417 | |||||||
chr9:27026490 | T | C | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.975-2535T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026490 | |||||||
chr9:27026572 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.975-2453G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026572 | |||||||
chr9:27026658 | A | C | 6 | a0001c0001t0001g0108 a0001c0001t0009g0031 a0001c0001t0009g0032 others(3): Show |
6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.975-2367A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026658 | |||||||
chr9:27026706 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.975-2319A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026706 | |||||||
chr9:27026829 | C | T | 10 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0006g0017 others(7): Show |
10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-2196C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026829 | |||||||
chr9:27026830 | T | G | 10 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0006g0017 others(7): Show |
10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-2195T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026830 | |||||||
chr9:27026846 | G | T | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.975-2179G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026846 | |||||||
chr9:27026859 | A | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG01192.hp1 HG02280.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.975-2166A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026859 | |||||||
chr9:27026899 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.975-2126G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026899 | |||||||
chr9:27027054 | A | C | 1 | a0006c0006t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.975-1971A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027054 | |||||||
chr9:27027146 | C | G | 17 | a0002c0002t0002g0052 a0002c0002t0002g0059 a0002c0002t0002g0077 others(14): Show |
17 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.975-1879C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027146 | |||||||
chr9:27027242 | T | C | 34 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(31): Show |
34 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.975-1783T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027242 | |||||||
chr9:27027414 | T | C | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.975-1611T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027414 | |||||||
chr9:27027808 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.975-1217A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027808 | |||||||
chr9:27027867 | T | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0034g0141 |
3 | HG01099.hp2 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.975-1158T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027867 | |||||||
chr9:27027940 | G | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.975-1085G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027940 | |||||||
chr9:27028163 | T | A | 2 | a0003c0003t0002g0043 a0003c0003t0002g0050 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.975-862T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028163 | |||||||
chr9:27028292 | C | G | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.975-733C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028292 | |||||||
chr9:27028383 | G | C | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.975-642G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028383 | |||||||
chr9:27028384 | G | C | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-641G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028384 | |||||||
chr9:27028433 | G | A | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.975-592G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028433 | |||||||
chr9:27028625 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG03041.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.975-400G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028625 | |||||||
chr9:27028669 | T | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.975-356T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028669 | |||||||
chr9:27028680 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.975-345C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028680 | |||||||
chr9:27028720 | A | C | 337 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(334): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.975-305A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028720 | |||||||
chr9:27028891 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0029g0159 |
2 | HG00423.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.975-134T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028891 | |||||||
chr9:27028949 | A | G | 31 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0138 others(28): Show |
31 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.975-76A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028949 | |||||||
chr9:27029107 | A | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.1054+3A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029107 | |||||||
chr9:27029249 | A | T | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+145A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029249 | |||||||
chr9:27029250 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+146C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029250 | |||||||
chr9:27029386 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1054+282G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029386 | |||||||
chr9:27029531 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1054+427G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029531 | |||||||
chr9:27029538 | G | A | 4 | a0002c0002t0002g0072 a0007c0007t0008g0004 a0007c0007t0008g0005 others(1): Show |
4 | HG01346.hp2 HG02615.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+434G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029538 | |||||||
chr9:27029605 | G | A | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1054+501G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029605 | |||||||
chr9:27029615 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0271 |
2 | NA18747.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1054+511G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029615 | |||||||
chr9:27029641 | G | A | 159 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(156): Show |
159 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1054+537G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029641 | |||||||
chr9:27029688 | C | T | 89 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(86): Show |
89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1054+584C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029688 | |||||||
chr9:27029750 | A | G | 1 | a0001c0001t0007g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1054+646A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029750 | |||||||
chr9:27029825 | T | C | 7 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(4): Show |
7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+721T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029825 | |||||||
chr9:27029889 | G | A | 7 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(4): Show |
7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+785G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029889 | |||||||
chr9:27030007 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1054+903A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030007 | |||||||
chr9:27030013 | T | C | 3 | a0007c0007t0006g0017 a0007c0007t0006g0026 a0007c0007t0006g0027 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1054+909T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030013 | |||||||
chr9:27030124 | C | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1054+1020C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030124 | |||||||
chr9:27030153 | G | A | 3 | a0002c0002t0002g0030 a0002c0002t0002g0045 a0002c0002t0002g0046 |
3 | HG00597.hp1 NA18988.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1054+1049G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030153 | |||||||
chr9:27030235 | A | G | 1 | a0002c0002t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1054+1131A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030235 | |||||||
chr9:27030291 | A | G | 5 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(2): Show |
5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+1187A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030291 | |||||||
chr9:27030350 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1054+1246C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030350 | |||||||
chr9:27030420 | T | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1054+1316T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030420 | |||||||
chr9:27030479 | C | T | 32 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(29): Show |
32 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1054+1375C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030479 | |||||||
chr9:27030542 | C | T | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1054+1438C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030542 | |||||||
chr9:27030547 | C | CA | 189 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0137 others(186): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1054+1461dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27030547 | ||||||
chr9:27030547 | C | CAA | 103 | a0001c0001t0001g0136 a0001c0001t0001g0209 a0001c0001t0001g0230 others(100): Show |
103 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1054+1460_1054+146 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27030547 | ||||||
chr9:27030547 | CA | C | 17 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(14): Show |
17 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1054+1461delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27030547 | ||||||
chr9:27030790 | T | A | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1054+1686T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030790 | |||||||
chr9:27030840 | A | G | 1 | a0004c0004t0004g0015 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1054+1736A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030840 | |||||||
chr9:27030858 | G | T | 1 | a0001c0001t0010g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1054+1754G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030858 | |||||||
chr9:27030929 | A | G | 2 | a0001c0001t0003g0294 a0001c0001t0003g0297 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1054+1825A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030929 | |||||||
chr9:27031283 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1054+2179G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031283 | |||||||
chr9:27031302 | TA | T | 10 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0006g0017 others(7): Show |
10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+2204delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031302 | ||||||
chr9:27031318 | T | C | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1054+2214T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031318 | |||||||
chr9:27031392 | A | G | 10 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0006g0017 others(7): Show |
10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+2288A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031392 | |||||||
chr9:27031461 | C | G | 5 | a0001c0001t0007g0135 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+2357C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031461 | |||||||
chr9:27031462 | G | A | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0155 others(5): Show |
8 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054+2358G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031462 | |||||||
chr9:27031485 | C | T | 91 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(88): Show |
91 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1054+2381C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031485 | |||||||
chr9:27031510 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1054+2406C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031510 | |||||||
chr9:27031549 | A | G | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1054+2445A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031549 | |||||||
chr9:27031560 | C | T | 5 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(2): Show |
5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+2456C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031560 | |||||||
chr9:27031576 | A | G | 1 | a0005c0005t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1054+2472A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031576 | |||||||
chr9:27031597 | A | AT | 30 | a0001c0001t0001g0109 a0001c0001t0001g0240 a0001c0001t0003g0002 others(27): Show |
31 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054+2510dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031597 | ||||||
chr9:27031597 | AT | A | 15 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(12): Show |
15 | HG01070.hp1 HG01192.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1054+2510delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031597 | ||||||
chr9:27031604 | T | C | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1054+2500T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031604 | |||||||
chr9:27031620 | G | GA | 3 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0305 |
3 | HG01243.hp1 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1054+2517dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031620 | ||||||
chr9:27031667 | A | C | 1 | a0003c0003t0002g0323 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1054+2563A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031667 | |||||||
chr9:27031732 | T | TAAATA | 76 | a0001c0001t0001g0122 a0001c0001t0001g0142 a0001c0001t0001g0153 others(73): Show |
77 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1054+2676_1054+268 others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | ||||||
chr9:27031732 | T | TAAATAAA others(3): Show |
57 | a0001c0001t0001g0130 a0001c0001t0001g0151 a0001c0001t0001g0189 others(54): Show |
57 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1054+2671_1054+268 others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | ||||||
chr9:27031732 | T | TAAATAAA others(8): Show |
13 | a0001c0001t0001g0214 a0001c0008t0001g0170 a0002c0002t0002g0030 others(10): Show |
13 | HG00558.hp2 HG00735.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1054+2666_1054+268 others(19): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | ||||||
chr9:27031732 | T | TAAATAAA others(13): Show |
1 | a0002c0002t0002g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1054+2661_1054+268 others(24): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | ||||||
chr9:27031732 | TAAATA | T | 60 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0129 others(57): Show |
60 | HG00558.hp1 HG00609.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1054+2676_1054+268 others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | ||||||
chr9:27031732 | TAAATAAA others(3): Show |
T | 18 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0165 others(15): Show |
18 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054+2671_1054+268 others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | ||||||
chr9:27031781 | T | TAAAATAA others(4): Show |
1 | a0002c0002t0002g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1054+2680_1054+268 others(15): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031781 | ||||||
chr9:27031781 | TAAATAAA others(15): Show |
T | 1 | a0001c0001t0003g0295 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1054+2702_1054+272 others(26): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031781 | ||||||
chr9:27031782 | AAATAAAA others(7): Show |
A | 2 | a0007c0007t0006g0017 a0007c0007t0006g0027 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1054+2679_1054+269 others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031782 | |||||||
chr9:27031796 | G | A | 8 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0006g0026 others(5): Show |
8 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054+2692G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031796 | |||||||
chr9:27031843 | G | C | 14 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1054+2739G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031843 | |||||||
chr9:27031897 | G | A | 159 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(156): Show |
159 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1054+2793G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031897 | |||||||
chr9:27031921 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1054+2817A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031921 | |||||||
chr9:27031925 | T | C | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1054+2821T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031925 | |||||||
chr9:27031972 | A | G | 1 | a0001c0001t0025g0177 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1054+2868A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031972 | |||||||
chr9:27032316 | T | G | 1 | a0004c0004t0004g0015 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1054+3212T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032316 | |||||||
chr9:27032320 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(5): Show |
8 | HG01192.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054+3216A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032320 | |||||||
chr9:27032334 | G | A | 26 | a0001c0001t0003g0002 a0001c0001t0003g0273 a0001c0001t0003g0274 others(23): Show |
27 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1054+3230G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032334 | |||||||
chr9:27032339 | C | T | 86 | a0001c0001t0002g0289 a0001c0001t0018g0128 a0002c0002t0002g0007 others(83): Show |
86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1054+3235C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032339 | |||||||
chr9:27032387 | G | A | 130 | a0001c0001t0002g0289 a0001c0001t0009g0031 a0001c0001t0009g0032 others(127): Show |
130 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1054+3283G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032387 | |||||||
chr9:27032532 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1054+3428A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032532 | |||||||
chr9:27032569 | T | TA | 25 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(22): Show |
25 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1054+3474dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27032569 | ||||||
chr9:27032622 | C | A | 5 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(2): Show |
5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+3518C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032622 | |||||||
chr9:27032791 | G | A | 1 | a0006c0006t0026g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1054+3687G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032791 | |||||||
chr9:27032810 | A | G | 7 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(4): Show |
7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+3706A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032810 | |||||||
chr9:27032821 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054+3717G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032821 | |||||||
chr9:27032827 | C | T | 5 | a0003c0003t0006g0113 a0003c0003t0006g0114 a0007c0007t0006g0017 others(2): Show |
5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+3723C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032827 | |||||||
chr9:27032914 | T | G | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1054+3810T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032914 | |||||||
chr9:27032923 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1054+3819C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032923 | |||||||
chr9:27032964 | G | A | 269 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(266): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1054+3860G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032964 | |||||||
chr9:27033210 | C | A | 1 | a0005c0005t0005g0313 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1054+4106C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033210 | |||||||
chr9:27033328 | G | C | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+4224G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033328 | |||||||
chr9:27033401 | A | AG | 3 | a0001c0001t0003g0291 a0001c0001t0003g0302 a0009c0014t0003g0292 |
3 | HG01952.hp1 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1054+4297_1054+429 others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033401 | |||||||
chr9:27033403 | AC | A | 5 | a0003c0003t0006g0113 a0003c0003t0006g0114 a0007c0007t0006g0017 others(2): Show |
5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+4300delC | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033403 | |||||||
chr9:27033560 | T | C | 1 | a0005c0005t0005g0313 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1054+4456T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033560 | |||||||
chr9:27033573 | C | CA | 20 | a0001c0001t0001g0108 a0001c0001t0001g0166 a0001c0001t0001g0167 others(17): Show |
20 | HG01123.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1054+4490dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | ||||||
chr9:27033573 | C | CAA | 14 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0309 others(11): Show |
14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1054+4489_1054+449 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | ||||||
chr9:27033573 | C | CAAAA | 12 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(9): Show |
12 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1054+4487_1054+449 others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | ||||||
chr9:27033573 | CA | C | 8 | a0001c0001t0001g0190 a0001c0001t0001g0232 a0001c0001t0001g0241 others(5): Show |
8 | HG00733.hp1 HG01070.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054+4490delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | ||||||
chr9:27033609 | C | T | 7 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(4): Show |
7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+4505C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033609 | |||||||
chr9:27033643 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | NA18612.hp1 NA18980.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1054+4539A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033643 | |||||||
chr9:27033649 | G | A | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+4545G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033649 | |||||||
chr9:27033702 | T | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+4598T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033702 | |||||||
chr9:27033744 | A | AT | 12 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0003c0003t0006g0113 others(9): Show |
12 | HG00733.hp1 HG01255.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054+4641dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033744 | ||||||
chr9:27033851 | G | T | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1054+4747G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033851 | |||||||
chr9:27033929 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1054+4825C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033929 | |||||||
chr9:27033962 | C | T | 4 | a0002c0002t0002g0123 a0002c0002t0002g0124 a0002c0002t0002g0125 others(1): Show |
4 | NA18991.hp2 NA19002.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+4858C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033962 | |||||||
chr9:27034108 | C | T | 1 | a0005c0005t0005g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1054+5004C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034108 | |||||||
chr9:27034152 | T | C | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+5048T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034152 | |||||||
chr9:27034291 | A | C | 1 | a0002c0002t0002g0059 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1054+5187A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034291 | |||||||
chr9:27034356 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1054+5252A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034356 | |||||||
chr9:27034515 | T | C | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054+5411T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034515 | |||||||
chr9:27034721 | G | A | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+5617G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034721 | |||||||
chr9:27034883 | T | C | 1 | a0002c0002t0002g0084 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1054+5779T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034883 | |||||||
chr9:27034972 | T | C | 3 | a0005c0005t0005g0314 a0005c0005t0005g0315 a0005c0005t0005g0316 |
3 | NA18957.hp1 NA18965.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1054+5868T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034972 | |||||||
chr9:27035013 | G | A | 5 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(2): Show |
5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+5909G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035013 | |||||||
chr9:27035167 | G | A | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+6063G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035167 | |||||||
chr9:27035246 | G | A | 9 | a0001c0001t0001g0130 a0001c0001t0001g0259 a0001c0001t0009g0031 others(6): Show |
9 | HG01255.hp2 HG01496.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+6142G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035246 | |||||||
chr9:27035907 | G | A | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1054+6803G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035907 | |||||||
chr9:27036023 | C | T | 1 | a0003c0003t0006g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1054+6919C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036023 | |||||||
chr9:27036067 | C | A | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+6963C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036067 | |||||||
chr9:27036143 | G | C | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+7039G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036143 | |||||||
chr9:27036200 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1054+7096A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036200 | |||||||
chr9:27036404 | T | A | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1054+7300T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036404 | |||||||
chr9:27036411 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054+7307A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036411 | |||||||
chr9:27036475 | A | G | 6 | a0001c0001t0001g0108 a0001c0001t0009g0031 a0001c0001t0009g0032 others(3): Show |
6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+7371A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036475 | |||||||
chr9:27036489 | C | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0338 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1054+7385C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036489 | |||||||
chr9:27036806 | G | A | 12 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0003c0003t0006g0113 others(9): Show |
12 | HG00733.hp1 HG01255.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054+7702G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036806 | |||||||
chr9:27037076 | C | T | 1 | a0006c0006t0026g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1055-7666C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037076 | |||||||
chr9:27037093 | A | G | 180 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(177): Show |
180 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.1055-7649A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037093 | |||||||
chr9:27037220 | C | CA | 95 | a0001c0001t0001g0108 a0001c0001t0001g0200 a0001c0001t0001g0230 others(92): Show |
95 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1055-7503dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27037220 | ||||||
chr9:27037220 | CA | C | 144 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(141): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1055-7503delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27037220 | ||||||
chr9:27037555 | G | A | 2 | a0005c0005t0005g0307 a0005c0005t0005g0308 |
2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1055-7187G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037555 | |||||||
chr9:27037760 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1055-6982A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037760 | |||||||
chr9:27037804 | T | C | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1055-6938T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037804 | |||||||
chr9:27037983 | T | C | 1 | a0008c0011t0001g0236 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1055-6759T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037983 | |||||||
chr9:27038055 | C | T | 1 | a0007c0007t0006g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1055-6687C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038055 | |||||||
chr9:27038088 | T | C | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-6654T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038088 | |||||||
chr9:27038128 | G | T | 2 | a0001c0001t0001g0153 a0001c0001t0020g0152 |
2 | HG02056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1055-6614G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038128 | |||||||
chr9:27038176 | A | G | 1 | a0003c0003t0002g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1055-6566A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038176 | |||||||
chr9:27038229 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1055-6513T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038229 | |||||||
chr9:27038375 | G | A | 2 | a0007c0007t0019g0119 a0007c0007t0023g0006 |
2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1055-6367G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038375 | |||||||
chr9:27038470 | C | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-6272C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038470 | |||||||
chr9:27038576 | C | A | 5 | a0003c0003t0006g0113 a0003c0003t0006g0114 a0007c0007t0006g0017 others(2): Show |
5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-6166C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038576 | |||||||
chr9:27038644 | C | T | 1 | a0006c0006t0026g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1055-6098C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038644 | |||||||
chr9:27038753 | A | T | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1055-5989A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038753 | |||||||
chr9:27038789 | A | G | 6 | a0001c0001t0001g0108 a0001c0001t0009g0031 a0001c0001t0009g0032 others(3): Show |
6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-5953A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038789 | |||||||
chr9:27038939 | A | G | 1 | a0002c0002t0002g0102 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1055-5803A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038939 | |||||||
chr9:27038950 | T | G | 91 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(88): Show |
91 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1055-5792T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038950 | |||||||
chr9:27039006 | T | C | 2 | a0001c0001t0010g0034 a0001c0001t0010g0035 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1055-5736T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039006 | |||||||
chr9:27039019 | C | T | 1 | a0002c0002t0002g0084 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1055-5723C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039019 | |||||||
chr9:27039251 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1055-5491G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039251 | |||||||
chr9:27039256 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0252 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1055-5486C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039256 | |||||||
chr9:27039348 | G | C | 2 | a0001c0001t0015g0131 a0001c0001t0015g0132 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1055-5394G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039348 | |||||||
chr9:27039450 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-5292A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039450 | |||||||
chr9:27039689 | G | C | 1 | a0002c0002t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1055-5053G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039689 | |||||||
chr9:27039728 | C | A | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1055-5014C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039728 | |||||||
chr9:27039982 | G | A | 2 | a0001c0001t0015g0131 a0001c0001t0015g0132 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1055-4760G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039982 | |||||||
chr9:27040256 | T | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1055-4486T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040256 | |||||||
chr9:27040299 | C | T | 1 | a0001c0001t0010g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1055-4443C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040299 | |||||||
chr9:27040544 | C | CA | 23 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(20): Show |
23 | HG01069.hp1 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1055-4175dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAA | 77 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0256 others(74): Show |
77 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1055-4176_1055-417 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAA | 12 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0002g0185 others(9): Show |
12 | HG01884.hp1 HG01978.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1055-4177_1055-417 others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAAAA | 21 | a0004c0004t0004g0014 a0004c0004t0004g0016 a0004c0004t0004g0018 others(18): Show |
21 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1055-4179_1055-417 others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0009g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1055-4188_1055-417 others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0009g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1055-4189_1055-417 others(19): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAAAAAA others(9): Show |
2 | a0003c0003t0002g0322 a0003c0003t0002g0323 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1055-4190_1055-417 others(20): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAAAAAA others(10): Show |
2 | a0003c0003t0002g0320 a0003c0003t0002g0321 |
2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1055-4191_1055-417 others(21): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0011g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1055-4175_1055-417 others(29): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0010g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1055-4175_1055-417 others(40): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | CA | C | 10 | a0001c0001t0001g0137 a0001c0001t0001g0160 a0001c0001t0001g0179 others(7): Show |
10 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1055-4175delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040544 | CAAAAAAA | C | 6 | a0003c0003t0006g0113 a0003c0003t0006g0114 a0007c0007t0006g0017 others(3): Show |
6 | HG00733.hp1 HG01255.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-4181_1055-417 others(11): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | ||||||
chr9:27040576 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1055-4166G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040576 | |||||||
chr9:27040936 | T | C | 1 | a0002c0002t0002g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1055-3806T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040936 | |||||||
chr9:27041070 | A | G | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1055-3672A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041070 | |||||||
chr9:27041092 | C | T | 2 | a0002c0002t0002g0042 a0003c0003t0002g0098 |
2 | NA19080.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1055-3650C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041092 | |||||||
chr9:27041174 | A | G | 1 | a0002c0002t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1055-3568A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041174 | |||||||
chr9:27041317 | C | T | 130 | a0001c0001t0002g0185 a0001c0001t0009g0031 a0001c0001t0009g0032 others(127): Show |
130 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1055-3425C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041317 | |||||||
chr9:27041334 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-3408A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041334 | |||||||
chr9:27041340 | A | G | 1 | a0003c0003t0022g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1055-3402A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041340 | |||||||
chr9:27041355 | A | C | 1 | a0001c0001t0001g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1055-3387A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041355 | |||||||
chr9:27041393 | A | G | 92 | a0001c0001t0002g0185 a0001c0001t0009g0031 a0001c0001t0009g0032 others(89): Show |
92 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1055-3349A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041393 | |||||||
chr9:27041501 | C | T | 86 | a0001c0001t0002g0185 a0001c0001t0018g0128 a0002c0002t0002g0007 others(83): Show |
86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1055-3241C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041501 | |||||||
chr9:27041518 | G | A | 1 | a0003c0003t0002g0127 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1055-3224G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041518 | |||||||
chr9:27041556 | G | A | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1055-3186G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041556 | |||||||
chr9:27041663 | G | A | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1055-3079G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041663 | |||||||
chr9:27041678 | C | T | 159 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(156): Show |
159 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1055-3064C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041678 | |||||||
chr9:27041834 | T | A | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1055-2908T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041834 | |||||||
chr9:27041835 | C | T | 2 | a0006c0006t0001g0325 a0006c0006t0001g0326 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-2907C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041835 | |||||||
chr9:27042163 | C | T | 3 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0036 |
3 | HG01884.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1055-2579C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042163 | |||||||
chr9:27042271 | A | G | 1 | a0001c0001t0002g0185 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1055-2471A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042271 | |||||||
chr9:27042359 | T | C | 3 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0019g0119 |
3 | HG01255.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1055-2383T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042359 | |||||||
chr9:27042398 | G | A | 14 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1055-2344G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042398 | |||||||
chr9:27042533 | A | G | 2 | a0001c0001t0011g0033 a0001c0001t0011g0036 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1055-2209A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042533 | |||||||
chr9:27042863 | A | G | 2 | a0002c0002t0002g0078 a0002c0002t0002g0080 |
2 | NA18980.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1055-1879A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042863 | |||||||
chr9:27042983 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1055-1759G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042983 | |||||||
chr9:27043002 | C | A | 1 | a0001c0012t0003g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1055-1740C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043002 | |||||||
chr9:27043130 | G | A | 10 | a0001c0001t0001g0154 a0001c0001t0001g0178 a0001c0001t0001g0181 others(7): Show |
10 | HG00597.hp2 HG02129.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1055-1612G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043130 | |||||||
chr9:27043644 | A | G | 2 | a0006c0006t0001g0325 a0006c0006t0001g0326 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-1098A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043644 | |||||||
chr9:27043916 | CTTCTCT | C | 4 | a0001c0001t0018g0128 a0001c0001t0033g0105 a0007c0007t0023g0006 others(1): Show |
4 | HG02886.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-823_1055-818d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27043916 | ||||||
chr9:27043925 | T | A | 4 | a0001c0001t0018g0128 a0001c0001t0033g0105 a0007c0007t0023g0006 others(1): Show |
4 | HG02886.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-817T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043925 | |||||||
chr9:27044327 | A | G | 3 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 |
3 | HG02630.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1055-415A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044327 | |||||||
chr9:27044493 | A | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1055-249A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044493 | |||||||
chr9:27044566 | A | T | 31 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0138 others(28): Show |
31 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.1055-176A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044566 | |||||||
chr9:27044589 | G | A | 15 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0153 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1055-153G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044589 | |||||||
chr9:27044645 | T | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1055-97T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044645 | |||||||
chr9:27045079 | A | G | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1108+284A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045079 | |||||||
chr9:27045219 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1108+424G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045219 | |||||||
chr9:27045260 | C | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1108+465C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045260 | |||||||
chr9:27045330 | A | G | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1108+535A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045330 | |||||||
chr9:27045344 | T | C | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1108+549T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045344 | |||||||
chr9:27045389 | A | G | 1 | a0006c0006t0026g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1108+594A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045389 | |||||||
chr9:27045639 | T | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1108+844T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045639 | |||||||
chr9:27045745 | A | G | 15 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(12): Show |
15 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1108+950A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045745 | |||||||
chr9:27045769 | A | T | 135 | a0001c0001t0002g0185 a0001c0001t0002g0289 a0001c0001t0009g0031 others(132): Show |
135 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1108+974A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045769 | |||||||
chr9:27045872 | T | C | 1 | a0002c0002t0002g0064 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1108+1077T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045872 | |||||||
chr9:27045985 | C | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1108+1190C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045985 | |||||||
chr9:27046279 | G | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1109-995G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046279 | |||||||
chr9:27046289 | A | G | 5 | a0003c0003t0006g0113 a0003c0003t0006g0114 a0007c0007t0006g0017 others(2): Show |
5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-985A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046289 | |||||||
chr9:27046343 | G | A | 134 | a0001c0001t0002g0185 a0001c0001t0009g0031 a0001c0001t0009g0032 others(131): Show |
134 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1109-931G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046343 | |||||||
chr9:27046443 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-831A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046443 | |||||||
chr9:27046470 | C | T | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1109-804C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046470 | |||||||
chr9:27046643 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1109-631A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046643 | |||||||
chr9:27046904 | G | A | 2 | a0003c0003t0002g0043 a0003c0003t0002g0050 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1109-370G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046904 | |||||||
chr9:27046945 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1109-329C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046945 | |||||||
chr9:27047008 | G | A | 134 | a0001c0001t0002g0185 a0001c0001t0009g0031 a0001c0001t0009g0032 others(131): Show |
134 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1109-266G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047008 | |||||||
chr9:27047077 | G | C | 1 | a0001c0001t0003g0299 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1109-197G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047077 | |||||||
chr9:27047120 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1109-154C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047120 | |||||||
chr9:27047123 | G | C | 1 | a0003c0003t0002g0098 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1109-151G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047123 | |||||||
chr9:27047160 | G | A | 4 | a0002c0002t0002g0051 a0002c0002t0002g0054 a0002c0002t0002g0067 others(1): Show |
4 | HG00735.hp2 HG01099.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-114G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047160 | |||||||
chr9:27047194 | A | T | 12 | a0006c0006t0001g0324 a0006c0006t0001g0325 a0006c0006t0001g0326 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1109-80A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047194 | |||||||
chr9:27047243 | A | T | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1109-31A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047243 | |||||||
chr9:27047248 | T | C | 269 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(266): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1109-26T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047248 | |||||||
chr9:27047462 | T | C | 28 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0209 others(25): Show |
28 | HG00609.hp2 HG00741.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1206+91T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047462 | |||||||
chr9:27047633 | AATT | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+268_1206+270d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr9 | 27047633 | ||||||
chr9:27047663 | T | C | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1206+292T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047663 | |||||||
chr9:27047784 | G | A | 4 | a0004c0004t0004g0014 a0004c0004t0004g0016 a0004c0004t0004g0022 others(1): Show |
4 | NA18960.hp2 NA18973.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-364G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047784 | |||||||
chr9:27047844 | C | T | 4 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0019g0119 others(1): Show |
4 | HG01255.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-304C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047844 | |||||||
chr9:27047940 | A | C | 1 | a0002c0002t0002g0051 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1207-208A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047940 | |||||||
chr9:27048313 | A | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(7): Show |
10 | HG01192.hp1 HG01255.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333+39A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048313 | |||||||
chr9:27048324 | A | G | 5 | a0001c0001t0001g0108 a0007c0007t0008g0004 a0007c0007t0008g0005 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+50A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048324 | |||||||
chr9:27048443 | T | C | 1 | a0002c0002t0002g0081 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1333+169T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048443 | |||||||
chr9:27048533 | T | A | 135 | a0001c0001t0001g0108 a0001c0001t0002g0185 a0001c0001t0002g0289 others(132): Show |
135 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1333+259T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048533 | |||||||
chr9:27048698 | A | G | 4 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0019g0119 others(1): Show |
4 | HG01255.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+424A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048698 | |||||||
chr9:27048736 | G | C | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1333+462G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048736 | |||||||
chr9:27048755 | T | G | 1 | a0001c0001t0001g0220 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1333+481T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048755 | |||||||
chr9:27048808 | C | T | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1333+534C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048808 | |||||||
chr9:27048896 | C | A | 1 | a0001c0001t0028g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+622C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048896 | |||||||
chr9:27048917 | T | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+643T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048917 | |||||||
chr9:27048963 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1333+689C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048963 | |||||||
chr9:27049027 | G | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+753G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049027 | |||||||
chr9:27049054 | A | G | 1 | a0002c0002t0002g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1333+780A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049054 | |||||||
chr9:27049111 | G | T | 1 | a0007c0007t0019g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1333+837G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049111 | |||||||
chr9:27049137 | T | C | 14 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333+863T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049137 | |||||||
chr9:27049272 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+998G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049272 | |||||||
chr9:27049306 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1032A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049306 | |||||||
chr9:27049377 | C | A | 1 | a0004c0004t0004g0025 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1333+1103C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049377 | |||||||
chr9:27049385 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1111C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049385 | |||||||
chr9:27049658 | A | G | 88 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(85): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1333+1384A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049658 | |||||||
chr9:27049661 | T | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1387T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049661 | |||||||
chr9:27049835 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1333+1561C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049835 | |||||||
chr9:27049864 | G | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+1590G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049864 | |||||||
chr9:27049940 | A | G | 14 | a0001c0001t0002g0289 a0002c0002t0002g0048 a0002c0002t0002g0049 others(11): Show |
14 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333+1666A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049940 | |||||||
chr9:27049966 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0035g0243 |
3 | HG01099.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1333+1692A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049966 | |||||||
chr9:27049979 | A | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+1705A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049979 | |||||||
chr9:27049989 | T | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1715T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049989 | |||||||
chr9:27049990 | A | G | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1716A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049990 | |||||||
chr9:27050009 | G | C | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1333+1735G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050009 | |||||||
chr9:27050025 | G | A | 30 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0004c0004t0004g0014 others(27): Show |
30 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1333+1751G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050025 | |||||||
chr9:27050046 | C | CTTAT | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
9 | HG01069.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1333+1797_1333+180 others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27050046 | ||||||
chr9:27050118 | C | T | 1 | a0002c0002t0002g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1333+1844C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050118 | |||||||
chr9:27050161 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1333+1887G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050161 | |||||||
chr9:27050595 | C | A | 32 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0138 others(29): Show |
32 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+2321C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050595 | |||||||
chr9:27050758 | A | G | 14 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0232 others(11): Show |
14 | HG01074.hp2 HG01243.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333+2484A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050758 | |||||||
chr9:27050768 | G | T | 14 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0232 others(11): Show |
14 | HG01074.hp2 HG01243.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333+2494G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050768 | |||||||
chr9:27050781 | T | C | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1333+2507T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050781 | |||||||
chr9:27050863 | A | T | 92 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(89): Show |
92 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1333+2589A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050863 | |||||||
chr9:27050874 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1333+2600T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050874 | |||||||
chr9:27051001 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1333+2727G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051001 | |||||||
chr9:27051043 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1333+2769T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051043 | |||||||
chr9:27051070 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1333+2796G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051070 | |||||||
chr9:27051192 | A | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1333+2918A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051192 | |||||||
chr9:27051215 | G | A | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1333+2941G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051215 | |||||||
chr9:27051428 | T | TA | 4 | a0003c0003t0002g0068 a0003c0003t0002g0101 a0003c0003t0021g0100 others(1): Show |
4 | HG02300.hp1 NA18964.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+3161dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27051428 | ||||||
chr9:27051524 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 |
3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1333+3250A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051524 | |||||||
chr9:27051814 | G | A | 139 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(136): Show |
139 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.1333+3540G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051814 | |||||||
chr9:27051876 | G | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01192.hp1 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333+3602G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051876 | |||||||
chr9:27051893 | G | C | 6 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(3): Show |
6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333+3619G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051893 | |||||||
chr9:27052179 | G | A | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-3430G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052179 | |||||||
chr9:27052307 | C | G | 2 | a0001c0001t0013g0266 a0001c0001t0013g0267 |
2 | NA18959.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1334-3302C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052307 | |||||||
chr9:27052327 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1334-3282T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052327 | |||||||
chr9:27052423 | A | C | 1 | a0001c0001t0032g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1334-3186A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052423 | |||||||
chr9:27052468 | A | G | 2 | a0003c0003t0002g0111 a0003c0003t0002g0112 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1334-3141A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052468 | |||||||
chr9:27052489 | C | T | 1 | a0005c0005t0005g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1334-3120C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052489 | |||||||
chr9:27052507 | C | CA | 25 | a0001c0001t0001g0107 a0001c0001t0001g0181 a0001c0001t0001g0184 others(22): Show |
25 | HG00733.hp1 HG01361.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1334-3079dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052507 | ||||||
chr9:27052507 | CA | C | 31 | a0001c0001t0001g0158 a0001c0001t0001g0221 a0001c0001t0001g0238 others(28): Show |
31 | HG00639.hp2 HG01069.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1334-3079delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052507 | ||||||
chr9:27052508 | A | C | 6 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
6 | NA18944.hp2 NA18966.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1334-3101A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052508 | |||||||
chr9:27052605 | C | G | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-3004C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052605 | |||||||
chr9:27052856 | A | ATGT | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0036 others(1): Show |
4 | HG01884.hp1 HG02080.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1334-2730_1334-272 others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052856 | ||||||
chr9:27052856 | ATGT | A | 3 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0023g0006 |
3 | HG03041.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1334-2730_1334-272 others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052856 | ||||||
chr9:27052930 | T | C | 4 | a0001c0001t0001g0151 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | HG01074.hp1 HG01175.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-2679T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052930 | |||||||
chr9:27053024 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1334-2585C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053024 | |||||||
chr9:27053124 | A | G | 2 | a0003c0003t0002g0091 a0003c0003t0002g0093 |
2 | NA18975.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1334-2485A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053124 | |||||||
chr9:27053161 | C | CT | 24 | a0001c0001t0001g0149 a0001c0001t0001g0186 a0001c0001t0001g0192 others(21): Show |
24 | HG00609.hp2 HG00639.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1334-2422dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053161 | ||||||
chr9:27053161 | CT | C | 186 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0107 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1334-2422delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053161 | ||||||
chr9:27053161 | CTT | C | 32 | a0001c0001t0001g0116 a0001c0001t0001g0138 a0002c0002t0002g0007 others(29): Show |
32 | HG00323.hp2 HG00733.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-2423_1334-242 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053161 | ||||||
chr9:27053227 | T | TTATA | 3 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0036 |
3 | HG01884.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1334-2380_1334-237 others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053227 | ||||||
chr9:27053263 | C | T | 1 | a0003c0003t0002g0098 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1334-2346C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053263 | |||||||
chr9:27053280 | A | T | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-2329A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053280 | |||||||
chr9:27053429 | T | G | 95 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0251 others(92): Show |
95 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1334-2180T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053429 | |||||||
chr9:27053481 | G | T | 2 | a0001c0001t0018g0128 a0011c0010t0017g0115 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-2128G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053481 | |||||||
chr9:27053652 | C | G | 132 | a0001c0001t0002g0185 a0001c0001t0009g0031 a0001c0001t0009g0032 others(129): Show |
132 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1334-1957C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053652 | |||||||
chr9:27053783 | T | A | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1334-1826T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053783 | |||||||
chr9:27053824 | G | A | 1 | a0001c0001t0014g0001 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1334-1785G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053824 | |||||||
chr9:27053897 | T | C | 1 | a0005c0005t0005g0317 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1334-1712T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053897 | |||||||
chr9:27053979 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1334-1630A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053979 | |||||||
chr9:27053990 | C | T | 330 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(327): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1334-1619C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053990 | |||||||
chr9:27054116 | G | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-1493G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054116 | |||||||
chr9:27054157 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG01192.hp1 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1334-1452G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054157 | |||||||
chr9:27054299 | C | T | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1334-1310C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054299 | |||||||
chr9:27054344 | A | G | 1 | a0005c0005t0005g0317 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1334-1265A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054344 | |||||||
chr9:27054668 | G | A | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG01069.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1334-941G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054668 | |||||||
chr9:27054697 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1334-912A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054697 | |||||||
chr9:27054791 | T | G | 1 | a0001c0001t0003g0288 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1334-818T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054791 | |||||||
chr9:27054854 | T | G | 2 | a0001c0001t0002g0289 a0001c0001t0016g0293 |
2 | HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1334-755T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054854 | |||||||
chr9:27054929 | A | T | 3 | a0004c0004t0004g0014 a0004c0004t0004g0016 a0004c0004t0004g0028 |
3 | NA18960.hp2 NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1334-680A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054929 | |||||||
chr9:27054959 | T | C | 28 | a0004c0004t0004g0014 a0004c0004t0004g0015 a0004c0004t0004g0016 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1334-650T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054959 | |||||||
chr9:27055013 | G | A | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1334-596G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055013 | |||||||
chr9:27055085 | G | C | 3 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0036 |
3 | HG01884.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1334-524G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055085 | |||||||
chr9:27055218 | T | G | 1 | a0002c0002t0002g0051 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1334-391T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055218 | |||||||
chr9:27055226 | A | AAT | 7 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0036 others(4): Show |
7 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1334-373_1334-372d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27055226 | ||||||
chr9:27055267 | T | C | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-342T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055267 | |||||||
chr9:27055285 | G | A | 127 | a0001c0001t0002g0185 a0001c0001t0009g0031 a0001c0001t0009g0032 others(124): Show |
127 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.1334-324G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055285 | |||||||
chr9:27055316 | T | C | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1334-293T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055316 | |||||||
chr9:27055512 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1334-97T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055512 | |||||||
chr9:27055540 | G | A | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1334-69G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055540 | |||||||
chr9:27055549 | T | A | 1 | a0001c0001t0011g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1334-60T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055549 | |||||||
chr9:27055568 | A | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(7): Show |
10 | HG01192.hp1 HG01255.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1334-41A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055568 | |||||||
chr9:27055844 | T | C | 2 | a0001c0001t0028g0300 a0010c0013t0031g0284 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1497+72T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/19 | chr9 | 27055844 | |||||||
chr9:27056147 | G | GTTA | 5 | a0003c0003t0006g0113 a0003c0003t0006g0114 a0007c0007t0006g0017 others(2): Show |
5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-183_1498-181d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr9 | 27056147 | ||||||
chr9:27056213 | A | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1498-121A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/19 | chr9 | 27056213 | |||||||
chr9:27056523 | A | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1623+64A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056523 | |||||||
chr9:27056731 | A | G | 1 | a0001c0001t0035g0243 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1623+272A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056731 | |||||||
chr9:27056789 | T | C | 1 | a0011c0010t0017g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1623+330T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056789 | |||||||
chr9:27056858 | G | GGATA | 52 | a0001c0001t0001g0106 a0001c0001t0001g0142 a0001c0001t0001g0143 others(49): Show |
52 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.1623+444_1623+447d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | ||||||
chr9:27056858 | G | GGATAGAT others(1): Show |
9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0163 others(6): Show |
9 | HG00099.hp2 HG00738.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1623+440_1623+447d others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | ||||||
chr9:27056858 | G | GGATAGAT others(5): Show |
2 | a0001c0001t0001g0181 a0002c0002t0002g0051 |
2 | NA18944.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1623+436_1623+447d others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | ||||||
chr9:27056858 | GGATA | G | 85 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0108 others(82): Show |
85 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1623+444_1623+447d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | ||||||
chr9:27056858 | GGATAGAT others(1): Show |
G | 35 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0144 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1623+440_1623+447d others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | ||||||
chr9:27056858 | GGATAGAT others(5): Show |
G | 5 | a0001c0001t0001g0263 a0001c0001t0009g0031 a0001c0001t0009g0032 others(2): Show |
5 | HG01099.hp1 HG01496.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623+436_1623+447d others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | ||||||
chr9:27056858 | GGATAGAT others(9): Show |
G | 1 | a0005c0005t0005g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1623+432_1623+447d others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | ||||||
chr9:27056958 | A | G | 1 | a0004c0004t0004g0021 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1623+499A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056958 | |||||||
chr9:27057247 | C | A | 1 | a0012c0009t0008g0003 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1623+788C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057247 | |||||||
chr9:27057255 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1623+796T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057255 | |||||||
chr9:27057457 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1623+998T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057457 | |||||||
chr9:27057543 | A | G | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1623+1084A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057543 | |||||||
chr9:27057645 | C | G | 1 | a0002c0002t0002g0044 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1623+1186C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057645 | |||||||
chr9:27057719 | G | A | 116 | a0001c0001t0002g0185 a0002c0002t0002g0007 a0002c0002t0002g0008 others(113): Show |
116 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1623+1260G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057719 | |||||||
chr9:27057743 | A | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1623+1284A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057743 | |||||||
chr9:27057750 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1623+1291C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057750 | |||||||
chr9:27058108 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1623+1649A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058108 | |||||||
chr9:27058123 | G | C | 305 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(302): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1623+1664G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058123 | |||||||
chr9:27058203 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1623+1744C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058203 | |||||||
chr9:27058273 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1623+1814G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058273 | |||||||
chr9:27058374 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1623+1915C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058374 | |||||||
chr9:27058459 | T | C | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1623+2000T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058459 | |||||||
chr9:27058562 | G | A | 134 | a0001c0001t0002g0185 a0001c0001t0002g0289 a0001c0001t0009g0031 others(131): Show |
134 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1624-2029G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058562 | |||||||
chr9:27058580 | G | A | 1 | a0005c0005t0005g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1624-2011G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058580 | |||||||
chr9:27058603 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1624-1988G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058603 | |||||||
chr9:27058638 | T | A | 5 | a0003c0003t0006g0113 a0003c0003t0006g0114 a0007c0007t0006g0017 others(2): Show |
5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1624-1953T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058638 | |||||||
chr9:27058920 | T | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0178 a0001c0001t0001g0181 others(6): Show |
9 | HG00597.hp2 HG02129.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1624-1671T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058920 | |||||||
chr9:27058975 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1624-1616C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058975 | |||||||
chr9:27059207 | T | C | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-1384T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059207 | |||||||
chr9:27059612 | A | G | 1 | a0002c0002t0002g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1624-979A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059612 | |||||||
chr9:27059621 | CTG | C | 10 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0264 others(7): Show |
10 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1624-969_1624-968d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059621 | |||||||
chr9:27059633 | G | A | 1 | a0008c0011t0001g0236 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1624-958G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059633 | |||||||
chr9:27059801 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1624-790C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059801 | |||||||
chr9:27059945 | A | G | 2 | a0005c0005t0005g0307 a0005c0005t0005g0308 |
2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1624-646A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059945 | |||||||
chr9:27060070 | G | T | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-521G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060070 | |||||||
chr9:27060212 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1624-379T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060212 | |||||||
chr9:27060323 | T | C | 2 | a0003c0003t0006g0113 a0003c0003t0006g0114 |
2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1624-268T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060323 | |||||||
chr9:27060346 | G | A | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1624-245G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060346 | |||||||
chr9:27060436 | TTTAA | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-153_1624-150d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27060436 | ||||||
chr9:27060457 | G | A | 6 | a0001c0001t0009g0031 a0001c0001t0009g0032 a0007c0007t0008g0004 others(3): Show |
6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-134G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060457 | |||||||
chr9:27060686 | C | T | 1 | a0002c0002t0002g0102 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1684+35C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060686 | |||||||
chr9:27060701 | A | G | 2 | a0003c0003t0002g0321 a0003c0003t0002g0322 |
2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1684+50A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060701 | |||||||
chr9:27060736 | G | A | 4 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+85G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060736 | |||||||
chr9:27060737 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1684+86C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060737 | |||||||
chr9:27060814 | T | C | 1 | a0001c0001t0033g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1684+163T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060814 | |||||||
chr9:27060823 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1684+172G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060823 | |||||||
chr9:27060848 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1684+197C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060848 | |||||||
chr9:27060884 | A | C | 5 | a0001c0001t0001g0108 a0007c0007t0008g0004 a0007c0007t0008g0005 others(2): Show |
5 | HG02615.hp1 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1684+233A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060884 | |||||||
chr9:27060927 | A | C | 1 | a0001c0001t0003g0298 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1684+276A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060927 | |||||||
chr9:27060940 | C | T | 1 | a0002c0002t0002g0063 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1684+289C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060940 | |||||||
chr9:27060961 | C | CA | 54 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0162 others(51): Show |
54 | HG00621.hp2 HG00639.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.1684+340dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | ||||||
chr9:27060961 | CA | C | 98 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0107 others(95): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1684+340delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | ||||||
chr9:27060961 | CAA | C | 8 | a0001c0001t0001g0104 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG01255.hp2 HG02273.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1684+339_1684+340d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | ||||||
chr9:27060961 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0303 |
3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1684+328_1684+340d others(15): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | ||||||
chr9:27060961 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1684+326_1684+340d others(17): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | ||||||
chr9:27060961 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1684+325_1684+340d others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | ||||||
chr9:27060980 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1684+329A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060980 | |||||||
chr9:27060990 | A | G | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1684+339A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060990 | |||||||
chr9:27061144 | G | GGT | 6 | a0005c0005t0005g0307 a0005c0005t0005g0308 a0005c0005t0005g0310 others(3): Show |
6 | HG01256.hp1 HG02735.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1684+517_1684+518d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061144 | ||||||
chr9:27061144 | GGT | G | 150 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0107 others(147): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1684+517_1684+518d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061144 | ||||||
chr9:27061144 | GGTGT | G | 98 | a0001c0001t0001g0103 a0001c0001t0002g0185 a0001c0001t0009g0031 others(95): Show |
98 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1684+515_1684+518d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061144 | ||||||
chr9:27061168 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1684+517T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061168 | |||||||
chr9:27061170 | C | T | 1 | a0007c0007t0023g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1684+519C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061170 | |||||||
chr9:27061174 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1684+523C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061174 | |||||||
chr9:27061335 | A | G | 1 | a0001c0001t0018g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1684+684A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061335 | |||||||
chr9:27061342 | C | A | 2 | a0001c0001t0011g0033 a0001c0001t0011g0036 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1684+691C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061342 | |||||||
chr9:27061385 | C | T | 83 | a0001c0001t0002g0185 a0002c0002t0002g0007 a0002c0002t0002g0008 others(80): Show |
83 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1684+734C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061385 | |||||||
chr9:27061386 | G | A | 4 | a0001c0001t0010g0034 a0001c0001t0010g0035 a0001c0001t0011g0033 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1684+735G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061386 | |||||||
chr9:27061394 | A | C | 2 | a0001c0001t0009g0031 a0001c0001t0009g0032 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1684+743A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061394 | |||||||
chr9:27061562 | A | G | 1 | a0001c0001t0010g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1684+911A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061562 | |||||||
chr9:27061677 | G | GTA | 43 | a0001c0001t0001g0106 a0001c0001t0001g0133 a0001c0001t0001g0134 others(40): Show |
43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.1685-923_1685-922d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATA | 15 | a0001c0001t0001g0158 a0001c0001t0001g0162 a0001c0001t0011g0036 others(12): Show |
15 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1685-925_1685-922d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATATA | 24 | a0001c0001t0011g0033 a0003c0003t0006g0113 a0003c0003t0006g0114 others(21): Show |
24 | HG00733.hp1 HG00733.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1685-927_1685-922d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATATAT others(1): Show |
6 | a0002c0002t0002g0040 a0002c0002t0002g0045 a0002c0002t0002g0046 others(3): Show |
6 | HG00597.hp1 HG03491.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1685-929_1685-922d others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATATAT others(3): Show |
54 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0009 others(51): Show |
54 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1685-931_1685-922d others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATATAT others(5): Show |
18 | a0002c0002t0002g0047 a0002c0002t0002g0048 a0002c0002t0002g0060 others(15): Show |
18 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1685-933_1685-922d others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATATAT others(7): Show |
2 | a0002c0002t0002g0057 a0002c0002t0002g0058 |
2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1685-935_1685-922d others(16): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATATAT others(9): Show |
4 | a0001c0001t0002g0185 a0001c0001t0018g0128 a0002c0002t0002g0059 others(1): Show |
4 | HG00621.hp2 HG03540.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685-937_1685-922d others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTATATAT others(11): Show |
1 | a0002c0002t0002g0052 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1685-939_1685-922d others(20): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061677 | G | GTGTATAT others(3): Show |
1 | a0002c0002t0002g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1685-940_1685-939i others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | ||||||
chr9:27061680 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1685-938T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061680 | |||||||
chr9:27061697 | G | A | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-921G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061697 | |||||||
chr9:27061700 | C | T | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-918C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061700 | |||||||
chr9:27061707 | T | TGTAC | 4 | a0003c0003t0002g0320 a0003c0003t0002g0321 a0003c0003t0002g0322 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-911_1685-910i others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061707 | |||||||
chr9:27061742 | A | G | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1685-876A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061742 | |||||||
chr9:27061904 | G | A | 1 | a0005c0005t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1685-714G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061904 | |||||||
chr9:27062344 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG03041.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1685-274A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062344 | |||||||
chr9:27062427 | G | A | 4 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0007c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685-191G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062427 | |||||||
chr9:27062478 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-140A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062478 | |||||||
chr9:27062486 | C | T | 3 | a0007c0007t0008g0004 a0007c0007t0008g0005 a0012c0009t0008g0003 |
3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1685-132C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062486 |