Item | Value |
---|---|
geneid | 348807 |
ensemblid | ENSG00000163885.12 |
hgncid | 26842 |
symbol | CFAP100 |
name | cilia and flagella associated protein 100 |
refseq_nuc | NM_182628.3 |
refseq_prot | NP_872434.2 |
ensembl_nuc | ENST00000352312.6 |
ensembl_prot | ENSP00000344749.1 |
mane_status | MANE Select |
chr | chr3 |
start | 126394909 |
end | 126436556 |
strand | + |
ver | v1.2 |
region | chr3:126394909-126436556 |
region5000 | chr3:126389909-126441556 |
regionname0 | CFAP100_chr3_126394909_126436556 |
regionname5000 | CFAP100_chr3_126389909_126441556 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 611 | 361 | 70 | 71 | 162 | 15 | 42 | 122 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0002 | 0/0 | 611 | 18 | 1 | 0 | 16 | 0 | 1 | 13 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0003 | 0/0 | 610 | 11 | 0 | 6 | 1 | 1 | 3 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(605): Show |
chr3 | 126389909 | 126441556 |
a0004 | 0/0 | 611 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0005 | 0/0 | 611 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0006 | 0/0 | 611 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0007 | 0/0 | 611 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0008 | 0/0 | 611 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0009 | 0/0 | 611 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0010 | 0/0 | 611 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0011 | 0/0 | 611 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIL others(606): Show |
chr3 | 126389909 | 126441556 |
a0012 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0013 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0014 | 0/0 | 611 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0015 | 0/0 | 611 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
a0016 | 0/1 | 611 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | MSEIP others(606): Show |
chr3 | 126389909 | 126441556 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1833 | 250 | 39 | 51 | 127 | 10 | 22 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0002 | 0/0 | 1833 | 65 | 6 | 16 | 19 | 5 | 19 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0003 | 0/0 | 1833 | 25 | 22 | 3 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0006 | 0/0 | 1833 | 10 | 0 | 0 | 10 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0008 | 0/0 | 1833 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0013 | 0/0 | 1833 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0016 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0018 | 0/0 | 1833 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0023 | 0/0 | 1833 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0001c0025 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0002c0004 | 0/0 | 1833 | 18 | 1 | 0 | 16 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0003c0005 | 0/0 | 1830 | 11 | 0 | 6 | 1 | 1 | 3 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1825): Show |
chr3 | 126389909 | 126441556 | ||
a0004c0007 | 0/0 | 1833 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0004c0028 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0005c0009 | 0/0 | 1833 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0005c0024 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0006c0010 | 0/0 | 1833 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0007c0011 | 0/0 | 1833 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0008c0014 | 0/0 | 1833 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0009c0017 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0009c0026 | 0/0 | 1833 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0010c0012 | 0/0 | 1833 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0011c0015 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0011c0029 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0012c0020 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0013c0021 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0014c0022 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0015c0019 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 | ||
a0016c0027 | 0/1 | 1833 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | ATGTC others(1828): Show |
chr3 | 126389909 | 126441556 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2117 | 241 | 36 | 50 | 125 | 8 | 21 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0001t0002 | 0/0 | 2117 | 7 | 3 | 1 | 0 | 2 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0001t0003 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0001t0005 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0002t0001 | 0/0 | 2117 | 63 | 6 | 14 | 19 | 5 | 19 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0002t0002 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0002t0004 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0003t0001 | 0/0 | 2117 | 25 | 22 | 3 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0006t0001 | 0/0 | 2117 | 10 | 0 | 0 | 10 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0008t0001 | 0/0 | 2117 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0013t0001 | 0/0 | 2117 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0016t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0018t0001 | 0/0 | 2117 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0023t0001 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0001c0025t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0002c0004t0001 | 0/0 | 2117 | 18 | 1 | 0 | 16 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0003c0005t0001 | 0/0 | 2114 | 11 | 0 | 6 | 1 | 1 | 3 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2109): Show |
chr3 | 126389909 | 126441556 |
a0004c0007t0001 | 0/0 | 2117 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0004c0028t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0005c0009t0001 | 0/0 | 2117 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0005c0009t0002 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0005c0024t0002 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0006c0010t0001 | 0/0 | 2117 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0007c0011t0002 | 0/0 | 2117 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0008c0014t0001 | 0/0 | 2117 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0009c0017t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0009c0026t0002 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0010c0012t0001 | 0/0 | 2117 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0011c0015t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0011c0029t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0012c0020t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0013c0021t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0014c0022t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0015c0019t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
a0016c0027t0001 | 0/1 | 2117 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | AAGAG others(2112): Show |
chr3 | 126389909 | 126441556 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0013t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0016t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0018t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0023t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0025t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0002 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0028t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0024t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0006c0010t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0006c0010t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0007c0011t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0007c0011t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0007c0011t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0008c0014t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0008c0014t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0009c0017t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0009c0026t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0010c0012t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0010c0012t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0011c0015t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0011c0029t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0012c0020t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0013c0021t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0014c0022t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0015c0019t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0016c0027t0001g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00140 | hp1 | a0003 | c0005 | t0001 | g0002 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0082 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0050 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00408 | hp2 | a0008 | c0014 | t0001 | g0247 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00544 | hp1 | a0002 | c0004 | t0001 | g0218 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00639 | hp1 | a0003 | c0005 | t0001 | g0235 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00733 | hp1 | a0006 | c0010 | t0001 | g0274 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01099 | hp1 | a0003 | c0005 | t0001 | g0002 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01106 | hp1 | a0003 | c0005 | t0001 | g0170 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01109 | hp1 | a0006 | c0010 | t0001 | g0022 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01243 | hp1 | a0003 | c0005 | t0001 | g0086 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0351 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01257 | hp2 | a0003 | c0005 | t0001 | g0167 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01258 | hp2 | a0003 | c0005 | t0001 | g0002 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01358 | hp2 | a0009 | c0026 | t0002 | g0027 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01361 | hp2 | a0001 | c0002 | t0004 | g0041 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0352 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01891 | hp1 | a0010 | c0012 | t0001 | g0068 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01993 | hp1 | a0001 | c0023 | t0001 | g0179 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0364 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02055 | hp2 | a0004 | c0007 | t0001 | g0135 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02080 | hp2 | a0002 | c0004 | t0001 | g0182 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02132 | hp1 | a0002 | c0004 | t0001 | g0025 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02145 | hp2 | a0005 | c0009 | t0001 | g0148 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0227 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02280 | hp1 | a0005 | c0009 | t0002 | g0058 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02280 | hp2 | a0005 | c0009 | t0001 | g0046 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0363 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02451 | hp2 | a0011 | c0029 | t0001 | g0079 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0139 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0367 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02622 | hp1 | a0010 | c0012 | t0001 | g0043 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0255 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02698 | hp2 | a0001 | c0018 | t0001 | g0319 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02738 | hp1 | a0003 | c0005 | t0001 | g0152 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02886 | hp2 | a0007 | c0011 | t0002 | g0169 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02895 | hp1 | a0001 | c0013 | t0001 | g0018 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02895 | hp2 | a0004 | c0007 | t0001 | g0019 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0110 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02896 | hp2 | a0012 | c0020 | t0001 | g0089 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02897 | hp2 | a0001 | c0013 | t0001 | g0018 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02922 | hp2 | a0005 | c0009 | t0001 | g0267 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02965 | hp1 | a0007 | c0011 | t0002 | g0234 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02976 | hp2 | a0001 | c0025 | t0001 | g0059 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03041 | hp1 | a0013 | c0021 | t0001 | g0069 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03098 | hp1 | a0005 | c0009 | t0001 | g0206 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03139 | hp1 | a0009 | c0017 | t0001 | g0147 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03209 | hp2 | a0007 | c0011 | t0002 | g0369 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03239 | hp2 | a0003 | c0005 | t0001 | g0002 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03453 | hp2 | a0004 | c0007 | t0001 | g0144 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0138 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03579 | hp1 | a0006 | c0010 | t0001 | g0022 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0366 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03688 | hp1 | a0003 | c0005 | t0001 | g0166 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0295 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0368 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03927 | hp2 | a0002 | c0004 | t0001 | g0212 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0324 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0067 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18944 | hp2 | a0001 | c0008 | t0001 | g0097 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18945 | hp1 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18951 | hp2 | a0002 | c0004 | t0001 | g0211 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18957 | hp1 | a0002 | c0004 | t0001 | g0215 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18965 | hp1 | a0002 | c0004 | t0001 | g0357 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18967 | hp1 | a0001 | c0006 | t0001 | g0266 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18967 | hp2 | a0001 | c0016 | t0001 | g0246 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18968 | hp1 | a0003 | c0005 | t0001 | g0331 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18969 | hp2 | a0002 | c0004 | t0001 | g0281 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18974 | hp1 | a0001 | c0008 | t0001 | g0098 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18977 | hp2 | a0001 | c0006 | t0001 | g0264 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18979 | hp2 | a0001 | c0008 | t0001 | g0099 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18980 | hp2 | a0002 | c0004 | t0001 | g0185 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18981 | hp1 | a0008 | c0014 | t0001 | g0074 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18987 | hp2 | a0011 | c0015 | t0001 | g0361 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18990 | hp1 | a0002 | c0004 | t0001 | g0025 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18995 | hp2 | a0002 | c0004 | t0001 | g0217 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18999 | hp2 | a0001 | c0006 | t0001 | g0029 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19000 | hp2 | a0002 | c0004 | t0001 | g0222 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19001 | hp1 | a0002 | c0004 | t0001 | g0358 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19001 | hp2 | a0001 | c0006 | t0001 | g0265 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19002 | hp2 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19011 | hp2 | a0002 | c0004 | t0001 | g0221 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19012 | hp2 | a0001 | c0008 | t0001 | g0013 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19043 | hp1 | a0005 | c0024 | t0002 | g0199 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19058 | hp1 | a0002 | c0004 | t0001 | g0219 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0346 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19060 | hp1 | a0014 | c0022 | t0001 | g0107 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19063 | hp1 | a0001 | c0006 | t0001 | g0029 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19065 | hp2 | a0001 | c0006 | t0001 | g0263 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19066 | hp1 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19076 | hp2 | a0001 | c0008 | t0001 | g0013 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19079 | hp2 | a0002 | c0004 | t0001 | g0216 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19081 | hp1 | a0015 | c0019 | t0001 | g0174 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19091 | hp2 | a0002 | c0004 | t0001 | g0122 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ASW | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ASW | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0026 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | GIH | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0359 | SAS | GIH | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02109 | hp1 | a0004 | c0007 | t0001 | g0060 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02109 | hp2 | a0004 | c0007 | t0001 | g0019 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03471 | hp1 | a0004 | c0007 | t0001 | g0254 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18955 | hp2 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA21309 | hp1 | a0002 | c0004 | t0001 | g0149 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA21309 | hp2 | a0004 | c0028 | t0001 | g0145 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
homoSapiens | chm13v2 | a0016 | c0027 | t0001 | g0081 | REF | REF | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0102 | REF | REF | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126396014 | C | A | 1 | a0011 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.14C>A | p.Pro5Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/17 | 143/2117 | 14/1836 | 5/611 | chr3 | 126396014 | |||
chr3:126396014 | C | T | 1 | a0011 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.14C>T | p.Pro5Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/17 | 143/2117 | 14/1836 | 5/611 | chr3 | 126396014 | |||
chr3:126414156 | C | A | 1 | a0002 | 18 | HG00544.hp1 HG02080.hp2 HG02132.hp1 others(15): Show |
missense_variant | MODERATE | c.202C>A | p.Gln68Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/17 | 331/2117 | 202/1836 | 68/611 | chr3 | 126414156 | |||
chr3:126416454 | G | A | 1 | a0015 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.364G>A | p.Glu122Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/17 | 493/2117 | 364/1836 | 122/611 | chr3 | 126416454 | |||
chr3:126418717 | C | G | 1 | a0004 | 7 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
missense_variant | MODERATE | c.593C>G | p.Ala198Gly | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 722/2117 | 593/1836 | 198/611 | chr3 | 126418717 | |||
chr3:126419122 | C | T | 1 | a0009 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.697C>T | p.Arg233Trp | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/17 | 826/2117 | 697/1836 | 233/611 | chr3 | 126419122 | |||
chr3:126419123 | G | A | 1 | a0009 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.698G>A | p.Arg233Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/17 | 827/2117 | 698/1836 | 233/611 | chr3 | 126419123 | |||
chr3:126420106 | G | A | 1 | a0007 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.959G>A | p.Gly320Asp | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1088/2117 | 959/1836 | 320/611 | chr3 | 126420106 | |||
chr3:126420145 | T | C | 2 | a0010 a0013 |
3 | HG01891.hp1 HG02622.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.998T>C | p.Met333Thr | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1127/2117 | 998/1836 | 333/611 | chr3 | 126420145 | |||
chr3:126420157 | G | A | 1 | a0006 | 3 | HG00733.hp1 HG01109.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.1010G>A | p.Arg337Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1139/2117 | 1010/1836 | 337/611 | chr3 | 126420157 | |||
chr3:126420181 | C | T | 1 | a0005 | 6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
missense_variant | MODERATE | c.1034C>T | p.Pro345Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1163/2117 | 1034/1836 | 345/611 | chr3 | 126420181 | |||
chr3:126423590 | CGGA | C | 1 | a0003 | 11 | HG00140.hp1 HG00639.hp1 HG01099.hp1 others(8): Show |
conservative_inframe_deletion | MODERATE | c.1234_1236delGAG | p.Glu412del | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/17 | 1363/2117 | 1234/1836 | 412/611 | INFO_REALIGN_3_PRIME | chr3 | 126423590 | ||
chr3:126423636 | G | T | 1 | a0008 | 2 | HG00408.hp2 NA18981.hp1 |
missense_variant | MODERATE | c.1278G>T | p.Gln426His | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/17 | 1407/2117 | 1278/1836 | 426/611 | chr3 | 126423636 | |||
chr3:126433184 | G | A | 1 | a0012 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1402G>A | p.Glu468Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/17 | 1531/2117 | 1402/1836 | 468/611 | chr3 | 126433184 | |||
chr3:126434222 | G | A | 1 | a0014 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1469G>A | p.Arg490Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/17 | 1598/2117 | 1469/1836 | 490/611 | chr3 | 126434222 | |||
chr3:126436375 | G | A | 1 | a0013 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1807G>A | p.Glu603Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 17/17 | 1936/2117 | 1807/1836 | 603/611 | chr3 | 126436375 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126396015 | G | A | 2 | a0001c0006 a0001c0016 |
11 | NA18945.hp1 NA18955.hp2 NA18967.hp1 others(8): Show |
synonymous_variant | LOW | c.15G>A | p.Pro5Pro | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/17 | 144/2117 | 15/1836 | 5/611 | chr3 | 126396015 | |||
chr3:126416340 | C | A | 1 | a0009c0017 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.250C>A | p.Arg84Arg | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/17 | 379/2117 | 250/1836 | 84/611 | chr3 | 126416340 | |||
chr3:126416366 | C | A | 1 | a0001c0018 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.276C>A | p.Ser92Ser | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/17 | 405/2117 | 276/1836 | 92/611 | chr3 | 126416366 | |||
chr3:126418613 | T | C | 2 | a0001c0003 a0012c0020 |
26 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(23): Show |
splice_region_variant&synonymous_variant | LOW | c.489T>C | p.Tyr163Tyr | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 618/2117 | 489/1836 | 163/611 | chr3 | 126418613 | |||
chr3:126418715 | C | T | 8 | a0001c0002 a0001c0003 a0001c0016 others(5): Show |
104 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
synonymous_variant | LOW | c.591C>T | p.Ala197Ala | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 720/2117 | 591/1836 | 197/611 | chr3 | 126418715 | |||
chr3:126418733 | C | T | 1 | a0001c0013 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.609C>T | p.Phe203Phe | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 738/2117 | 609/1836 | 203/611 | chr3 | 126418733 | |||
chr3:126419694 | A | C | 1 | a0001c0025 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.789A>C | p.Leu263Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 9/17 | 918/2117 | 789/1836 | 263/611 | chr3 | 126419694 | |||
chr3:126423567 | G | A | 1 | a0004c0028 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1209G>A | p.Ser403Ser | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/17 | 1338/2117 | 1209/1836 | 403/611 | chr3 | 126423567 | |||
chr3:126433138 | C | T | 1 | a0001c0023 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1356C>T | p.Asp452Asp | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/17 | 1485/2117 | 1356/1836 | 452/611 | chr3 | 126433138 | |||
chr3:126434259 | C | T | 1 | a0005c0024 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1506C>T | p.Gly502Gly | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/17 | 1635/2117 | 1506/1836 | 502/611 | chr3 | 126434259 | |||
chr3:126434307 | A | G | 2 | a0001c0008 a0014c0022 |
6 | NA18944.hp2 NA18974.hp1 NA18979.hp2 others(3): Show |
synonymous_variant | LOW | c.1554A>G | p.Leu518Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/17 | 1683/2117 | 1554/1836 | 518/611 | chr3 | 126434307 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126394928 | C | G | 1 | a0001c0001t0005 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/17 | 1073 | chr3 | 126394928 | ||||||
chr3:126394958 | G | C | 1 | a0001c0001t0003 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/17 | 1043 | chr3 | 126394958 | ||||||
chr3:126394959 | A | G | 1 | a0001c0002t0004 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/17 | 1042 | chr3 | 126394959 | ||||||
chr3:126436482 | C | T | 6 | a0001c0001t0002 a0001c0002t0002 a0005c0009t0002 others(3): Show |
14 | HG01099.hp2 HG01358.hp2 HG01981.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*78C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 17/17 | 78 | chr3 | 126436482 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126395010 | C | A | 1 | a0001c0001t0001g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-60+32C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395010 | |||||||
chr3:126395039 | C | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(11): Show |
15 | HG00323.hp2 HG00733.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-60+61C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395039 | |||||||
chr3:126395039 | C | T | 1 | a0007c0011t0002g0369 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-60+61C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395039 | |||||||
chr3:126395042 | C | T | 2 | a0001c0002t0001g0367 a0001c0002t0001g0368 |
2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-60+64C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395042 | |||||||
chr3:126395099 | A | G | 1 | a0001c0002t0001g0366 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-60+121A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395099 | |||||||
chr3:126395252 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-60+274G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395252 | |||||||
chr3:126395399 | A | G | 1 | a0001c0001t0001g0365 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-60+421A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395399 | |||||||
chr3:126395613 | G | T | 6 | a0001c0001t0001g0362 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
7 | HG01361.hp2 HG01928.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-59-329G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395613 | |||||||
chr3:126395803 | T | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0056 |
3 | HG02886.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-59-139T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395803 | |||||||
chr3:126395864 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-59-78G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395864 | |||||||
chr3:126396058 | C | T | 1 | a0001c0002t0001g0039 | 2 | HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.49+9C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396058 | |||||||
chr3:126396092 | A | G | 1 | a0011c0015t0001g0361 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.49+43A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396092 | |||||||
chr3:126396099 | G | A | 2 | a0001c0001t0001g0042 a0005c0009t0002g0058 |
2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.49+50G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396099 | |||||||
chr3:126396277 | G | C | 2 | a0001c0025t0001g0059 a0004c0007t0001g0060 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.49+228G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396277 | |||||||
chr3:126396313 | G | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.49+264G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396313 | |||||||
chr3:126396511 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG01261.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.49+462G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396511 | |||||||
chr3:126396522 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.49+473C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396522 | |||||||
chr3:126396565 | C | G | 1 | a0001c0003t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+516C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396565 | |||||||
chr3:126396569 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.49+520A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396569 | |||||||
chr3:126396647 | A | C | 1 | a0001c0002t0001g0368 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.49+598A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396647 | |||||||
chr3:126396661 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.49+612G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396661 | |||||||
chr3:126396773 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.49+724G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396773 | |||||||
chr3:126396805 | C | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0232 others(2): Show |
6 | HG00738.hp2 HG01168.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+756C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396805 | |||||||
chr3:126396827 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.49+778G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396827 | |||||||
chr3:126396875 | T | A | 1 | a0007c0011t0002g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49+826T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396875 | |||||||
chr3:126396905 | A | T | 1 | a0001c0002t0001g0359 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.49+856A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396905 | |||||||
chr3:126396940 | C | T | 21 | a0001c0001t0001g0024 a0001c0001t0001g0210 a0001c0001t0001g0213 others(18): Show |
23 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.49+891C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396940 | |||||||
chr3:126397052 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.49+1003T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397052 | |||||||
chr3:126397290 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.49+1241T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397290 | |||||||
chr3:126397336 | C | T | 15 | a0001c0001t0001g0055 a0001c0001t0001g0196 a0001c0001t0001g0198 others(12): Show |
15 | HG01109.hp2 HG02572.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+1287C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397336 | |||||||
chr3:126397345 | G | A | 14 | a0001c0001t0001g0055 a0001c0001t0001g0196 a0001c0001t0001g0198 others(11): Show |
14 | HG01109.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1296G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397345 | |||||||
chr3:126397348 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.49+1299C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397348 | |||||||
chr3:126397349 | T | C | 20 | a0001c0001t0001g0044 a0001c0001t0001g0055 a0001c0001t0001g0196 others(17): Show |
20 | HG01109.hp2 HG01891.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.49+1300T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397349 | |||||||
chr3:126397567 | C | A | 25 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0056 others(22): Show |
30 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.49+1518C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397567 | |||||||
chr3:126397590 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.49+1541G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397590 | |||||||
chr3:126397744 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.49+1695G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397744 | |||||||
chr3:126397867 | C | T | 1 | a0004c0007t0001g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+1818C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397867 | |||||||
chr3:126397891 | G | A | 1 | a0001c0002t0001g0240 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.49+1842G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397891 | |||||||
chr3:126397961 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+1912G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397961 | |||||||
chr3:126398268 | G | A | 1 | a0004c0007t0001g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+2219G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398268 | |||||||
chr3:126398288 | G | A | 1 | a0004c0007t0001g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+2239G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398288 | |||||||
chr3:126398307 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+2258G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398307 | |||||||
chr3:126398312 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+2263C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398312 | |||||||
chr3:126398316 | T | C | 11 | a0001c0001t0001g0088 a0001c0001t0002g0027 a0001c0001t0002g0241 others(8): Show |
12 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+2267T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398316 | |||||||
chr3:126398429 | A | G | 313 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(310): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.49+2380A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398429 | |||||||
chr3:126398459 | C | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(5): Show |
11 | HG00741.hp2 HG02083.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+2410C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398459 | |||||||
chr3:126398593 | T | C | 2 | a0001c0003t0001g0005 a0004c0007t0001g0060 |
4 | HG01255.hp2 HG02109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+2544T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398593 | |||||||
chr3:126398697 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.49+2648C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398697 | |||||||
chr3:126398717 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.49+2668A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398717 | |||||||
chr3:126398827 | G | A | 2 | a0004c0007t0001g0135 a0004c0007t0001g0254 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+2778G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398827 | |||||||
chr3:126398879 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+2830G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398879 | |||||||
chr3:126398907 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.49+2858C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398907 | |||||||
chr3:126398923 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.49+2874A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398923 | |||||||
chr3:126399120 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+3071C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399120 | |||||||
chr3:126399160 | C | T | 5 | a0001c0001t0001g0088 a0001c0001t0001g0208 a0001c0003t0001g0087 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3111C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399160 | |||||||
chr3:126399274 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.49+3225G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399274 | |||||||
chr3:126399453 | A | G | 28 | a0001c0001t0001g0024 a0001c0001t0001g0193 a0001c0001t0001g0194 others(25): Show |
30 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.49+3404A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399453 | |||||||
chr3:126399718 | A | G | 6 | a0001c0001t0002g0027 a0001c0001t0002g0241 a0001c0001t0002g0242 others(3): Show |
6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+3669A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399718 | |||||||
chr3:126399885 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0365 |
2 | NA18971.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.49+3836G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399885 | |||||||
chr3:126399885 | G | C | 1 | a0001c0003t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+3836G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399885 | |||||||
chr3:126399946 | G | C | 11 | a0001c0001t0001g0017 a0001c0001t0001g0140 a0001c0001t0001g0141 others(8): Show |
19 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.49+3897G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399946 | |||||||
chr3:126399978 | G | A | 1 | a0004c0007t0001g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+3929G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399978 | |||||||
chr3:126400027 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49+3978C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400027 | |||||||
chr3:126400062 | C | T | 1 | a0004c0007t0001g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+4013C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400062 | |||||||
chr3:126400091 | T | C | 14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0229 others(11): Show |
15 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+4042T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400091 | |||||||
chr3:126400126 | A | G | 1 | a0001c0001t0001g0353 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.49+4077A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400126 | |||||||
chr3:126400460 | A | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0200 others(8): Show |
11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+4411A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400460 | |||||||
chr3:126400525 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.49+4476G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400525 | |||||||
chr3:126400529 | G | A | 5 | a0004c0007t0001g0019 a0004c0007t0001g0135 a0004c0007t0001g0144 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+4480G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400529 | |||||||
chr3:126400549 | T | C | 34 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0001c0001t0001g0065 others(31): Show |
42 | HG00738.hp2 HG01081.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.49+4500T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400549 | |||||||
chr3:126400549 | T | G | 6 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0006c0010t0001g0274 others(3): Show |
6 | HG00733.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+4500T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400549 | |||||||
chr3:126400568 | A | G | 2 | a0001c0002t0001g0258 a0001c0002t0001g0259 |
2 | NA18947.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.49+4519A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400568 | |||||||
chr3:126400569 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.49+4520T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400569 | |||||||
chr3:126400604 | T | C | 3 | a0001c0001t0001g0088 a0001c0003t0001g0087 a0001c0003t0001g0227 |
3 | HG01243.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.49+4555T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400604 | |||||||
chr3:126400606 | A | G | 145 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0030 others(142): Show |
161 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.49+4557A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400606 | |||||||
chr3:126400620 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.49+4571C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400620 | |||||||
chr3:126400646 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.49+4597G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400646 | |||||||
chr3:126400668 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0238 |
2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.49+4619C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400668 | |||||||
chr3:126400709 | G | A | 1 | a0003c0005t0001g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.49+4660G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400709 | |||||||
chr3:126400717 | A | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0332 others(8): Show |
15 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+4668A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400717 | |||||||
chr3:126400751 | C | CA | 17 | a0001c0001t0001g0021 a0001c0001t0001g0091 a0001c0001t0001g0168 others(14): Show |
22 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.49+4712dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126400751 | ||||||
chr3:126400788 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0065 others(7): Show |
11 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+4739C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400788 | |||||||
chr3:126400855 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49+4806C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400855 | |||||||
chr3:126400855 | C | T | 4 | a0001c0002t0001g0192 a0001c0002t0001g0352 a0001c0002t0001g0366 others(1): Show |
4 | HG01099.hp2 HG01433.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+4806C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400855 | |||||||
chr3:126400910 | A | G | 11 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0200 others(8): Show |
11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+4861A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400910 | |||||||
chr3:126400942 | C | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0083 others(13): Show |
27 | HG00323.hp1 HG00741.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+4893C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400942 | |||||||
chr3:126401005 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.49+4956C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401005 | |||||||
chr3:126401039 | A | G | 1 | a0001c0013t0001g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+4990A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401039 | |||||||
chr3:126401070 | A | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0200 others(8): Show |
11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+5021A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401070 | |||||||
chr3:126401091 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.49+5042C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401091 | |||||||
chr3:126401104 | A | C | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.49+5055A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401104 | |||||||
chr3:126401170 | G | A | 1 | a0001c0002t0001g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.49+5121G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401170 | |||||||
chr3:126401209 | G | A | 300 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(297): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.49+5160G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401209 | |||||||
chr3:126401360 | A | G | 28 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0261 others(25): Show |
35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.49+5311A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401360 | |||||||
chr3:126401394 | A | ATT | 15 | a0001c0001t0001g0037 a0001c0001t0001g0072 a0001c0001t0001g0164 others(12): Show |
16 | HG00140.hp2 HG00673.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+5348_49+5349dup others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401394 | ||||||
chr3:126401396 | TTTATATA others(8): Show |
T | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.49+5349_49+5363del others(15): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401396 | ||||||
chr3:126401397 | T | TTA | 36 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(33): Show |
37 | HG00558.hp2 HG00741.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.49+5393_49+5394dup others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTATA | 29 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(26): Show |
30 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.49+5391_49+5394dup others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTATATA | 10 | a0001c0001t0001g0015 a0001c0001t0001g0077 a0001c0001t0001g0118 others(7): Show |
11 | HG00408.hp2 HG00597.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+5389_49+5394dup others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTATATAT others(1): Show |
9 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0088 others(6): Show |
9 | HG01168.hp1 HG01261.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5387_49+5394dup others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0093 a0001c0001t0001g0323 a0001c0002t0001g0010 others(1): Show |
4 | HG02886.hp2 NA18988.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+5385_49+5394dup others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.49+5383_49+5394dup others(12): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTA | 32 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0034 others(29): Show |
34 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTATA | 25 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(22): Show |
26 | HG00544.hp2 HG00558.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTATAT others(1): Show |
13 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(10): Show |
13 | HG00408.hp1 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTATAT others(3): Show |
5 | a0001c0001t0001g0066 a0001c0001t0001g0276 a0001c0001t0001g0289 others(2): Show |
5 | HG00099.hp1 NA18963.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTATAT others(5): Show |
1 | a0001c0001t0001g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(12): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTATAT others(9): Show |
1 | a0001c0001t0001g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(16): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTATAT others(11): Show |
1 | a0002c0004t0001g0358 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(18): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | T | TTTTATAT others(19): Show |
1 | a0001c0001t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(26): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTA | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0031 others(28): Show |
32 | HG00280.hp1 HG00544.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.49+5393_49+5394del others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATA | T | 13 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0117 others(10): Show |
14 | HG01106.hp1 HG01243.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+5391_49+5394del others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATA | T | 6 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0329 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+5389_49+5394del others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(1): Show |
T | 3 | a0001c0002t0001g0084 a0004c0007t0001g0019 a0004c0028t0001g0145 |
3 | HG02895.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.49+5387_49+5394del others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(3): Show |
T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0171 a0001c0002t0001g0111 others(1): Show |
4 | HG00738.hp2 HG01175.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+5385_49+5394del others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(5): Show |
T | 10 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0196 others(7): Show |
12 | HG00323.hp2 HG01070.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+5383_49+5394del others(12): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(7): Show |
T | 4 | a0001c0001t0001g0190 a0001c0002t0001g0038 a0001c0002t0001g0359 others(1): Show |
4 | HG01099.hp2 HG02683.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+5381_49+5394del others(14): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(9): Show |
T | 10 | a0001c0001t0001g0173 a0001c0001t0001g0339 a0001c0002t0001g0038 others(7): Show |
10 | HG01433.hp1 HG02080.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+5379_49+5394del others(16): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(11): Show |
T | 39 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0159 others(36): Show |
41 | HG00735.hp1 HG01074.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.49+5377_49+5394del others(18): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(13): Show |
T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0344 a0001c0001t0001g0348 others(2): Show |
5 | HG01993.hp1 HG01993.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+5375_49+5394del others(20): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(17): Show |
T | 2 | a0001c0001t0001g0239 a0001c0002t0001g0049 |
2 | HG00597.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.49+5371_49+5394del others(24): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(19): Show |
T | 27 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0261 others(24): Show |
34 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(31): Show |
intron_variant | MODIFIER | c.49+5369_49+5394del others(26): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(21): Show |
T | 14 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0309 others(11): Show |
14 | HG00609.hp1 HG02040.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+5367_49+5394del others(28): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401397 | TTATATAT others(33): Show |
T | 2 | a0001c0001t0001g0208 a0012c0020t0001g0089 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.49+5355_49+5394del others(40): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | ||||||
chr3:126401398 | TATATATA others(22): Show |
T | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.49+5350_49+5378del others(29): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401398 | |||||||
chr3:126401399 | A | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0036 others(8): Show |
13 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+5350A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401399 | |||||||
chr3:126401401 | A | T | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0056 others(5): Show |
9 | HG00544.hp1 HG02071.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5352A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401401 | |||||||
chr3:126401403 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.49+5354A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401403 | |||||||
chr3:126401405 | A | T | 1 | a0003c0005t0001g0331 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.49+5356A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401405 | |||||||
chr3:126401407 | A | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+5358A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401407 | |||||||
chr3:126401411 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.49+5362A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401411 | |||||||
chr3:126401417 | A | T | 1 | a0003c0005t0001g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.49+5368A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401417 | |||||||
chr3:126401423 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.49+5374A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401423 | |||||||
chr3:126401427 | A | T | 12 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0309 others(9): Show |
12 | HG00609.hp1 HG02040.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+5378A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401427 | |||||||
chr3:126401429 | A | T | 13 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0275 others(10): Show |
13 | HG00609.hp1 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+5380A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401429 | |||||||
chr3:126401476 | T | C | 2 | a0004c0007t0001g0135 a0004c0007t0001g0254 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+5427T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401476 | |||||||
chr3:126401511 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49+5462A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401511 | |||||||
chr3:126401516 | C | T | 5 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0010c0012t0001g0043 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+5467C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401516 | |||||||
chr3:126401589 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49+5540A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401589 | |||||||
chr3:126401691 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0241 a0001c0001t0002g0242 others(3): Show |
6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-5481G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401691 | |||||||
chr3:126401701 | A | G | 294 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(291): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.50-5471A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401701 | |||||||
chr3:126401757 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(112): Show |
131 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.50-5415G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401757 | |||||||
chr3:126401806 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-5366G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401806 | |||||||
chr3:126401811 | T | C | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | NA18964.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.50-5361T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401811 | |||||||
chr3:126401901 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(109): Show |
127 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.50-5271C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401901 | |||||||
chr3:126401957 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.50-5215C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401957 | |||||||
chr3:126402144 | G | A | 6 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0002t0001g0084 others(3): Show |
6 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-5028G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402144 | |||||||
chr3:126402170 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.50-5002G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402170 | |||||||
chr3:126402362 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG00733.hp2 HG01071.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-4810G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402362 | |||||||
chr3:126402370 | G | A | 2 | a0001c0001t0001g0208 a0012c0020t0001g0089 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.50-4802G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402370 | |||||||
chr3:126402373 | G | A | 1 | a0001c0002t0001g0363 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.50-4799G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402373 | |||||||
chr3:126402550 | G | A | 1 | a0012c0020t0001g0089 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50-4622G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402550 | |||||||
chr3:126402694 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0241 a0001c0001t0002g0242 others(3): Show |
6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-4478G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402694 | |||||||
chr3:126402783 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.50-4389C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402783 | |||||||
chr3:126402827 | G | A | 8 | a0001c0003t0001g0001 a0001c0003t0001g0016 a0001c0003t0001g0028 others(5): Show |
15 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.50-4345G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402827 | |||||||
chr3:126402949 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG01081.hp1 HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.50-4223C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402949 | |||||||
chr3:126403080 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.50-4092G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403080 | |||||||
chr3:126403128 | T | C | 5 | a0004c0007t0001g0019 a0004c0007t0001g0135 a0004c0007t0001g0144 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-4044T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403128 | |||||||
chr3:126403150 | C | T | 1 | a0006c0010t0001g0274 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.50-4022C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403150 | |||||||
chr3:126403187 | A | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0200 others(8): Show |
11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-3985A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403187 | |||||||
chr3:126403209 | C | T | 2 | a0001c0001t0001g0208 a0012c0020t0001g0089 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.50-3963C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403209 | |||||||
chr3:126403210 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0066 |
5 | NA18998.hp2 NA19009.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-3962G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403210 | |||||||
chr3:126403267 | C | T | 1 | a0013c0021t0001g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.50-3905C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403267 | |||||||
chr3:126403268 | G | A | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0257 others(4): Show |
8 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-3904G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403268 | |||||||
chr3:126403318 | C | T | 29 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(26): Show |
31 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.50-3854C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403318 | |||||||
chr3:126403319 | G | C | 1 | a0001c0001t0002g0241 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.50-3853G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403319 | |||||||
chr3:126403383 | C | CT | 23 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0057 others(20): Show |
25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-3770dupT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | ||||||
chr3:126403383 | C | CTT | 13 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0088 others(10): Show |
17 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-3771_50-3770dup others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | ||||||
chr3:126403383 | CT | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.50-3770delT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | ||||||
chr3:126403383 | CTT | C | 10 | a0001c0001t0001g0193 a0001c0001t0001g0208 a0001c0001t0001g0278 others(7): Show |
10 | HG01981.hp1 HG02451.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-3771_50-3770del others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | ||||||
chr3:126403453 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.50-3719C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403453 | |||||||
chr3:126403470 | C | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.50-3702C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403470 | |||||||
chr3:126403646 | G | A | 1 | a0001c0001t0001g0360 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.50-3526G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403646 | |||||||
chr3:126403700 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-3472T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403700 | |||||||
chr3:126403730 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.50-3442T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403730 | |||||||
chr3:126403789 | T | C | 1 | a0001c0002t0001g0251 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50-3383T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403789 | |||||||
chr3:126403829 | C | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.50-3343C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403829 | |||||||
chr3:126403847 | A | G | 1 | a0011c0029t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.50-3325A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403847 | |||||||
chr3:126404022 | G | C | 1 | a0005c0009t0002g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-3150G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404022 | |||||||
chr3:126404041 | C | G | 1 | a0001c0003t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-3131C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404041 | |||||||
chr3:126404042 | G | A | 2 | a0001c0001t0001g0208 a0012c0020t0001g0089 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.50-3130G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404042 | |||||||
chr3:126404106 | G | T | 28 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0261 others(25): Show |
35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.50-3066G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404106 | |||||||
chr3:126404133 | C | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0241 a0001c0001t0002g0242 others(3): Show |
6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-3039C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404133 | |||||||
chr3:126404278 | G | C | 2 | a0001c0001t0001g0213 a0002c0004t0001g0212 |
2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.50-2894G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404278 | |||||||
chr3:126404389 | T | C | 1 | a0003c0005t0001g0170 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.50-2783T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404389 | |||||||
chr3:126404431 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.50-2741A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404431 | |||||||
chr3:126404654 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.50-2518C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404654 | |||||||
chr3:126404754 | A | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG00733.hp2 HG01071.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-2418A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404754 | |||||||
chr3:126404832 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(38): Show |
57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.50-2340G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404832 | |||||||
chr3:126404877 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50-2295G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404877 | |||||||
chr3:126404964 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0256 others(2): Show |
8 | HG00323.hp1 HG00741.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-2208C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404964 | |||||||
chr3:126404966 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-2206G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404966 | |||||||
chr3:126405085 | GACC | G | 28 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0261 others(25): Show |
35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.50-2079_50-2077del others(3): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126405085 | ||||||
chr3:126405122 | A | G | 54 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0159 others(51): Show |
57 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-2050A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405122 | |||||||
chr3:126405298 | C | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0276 others(3): Show |
8 | HG02071.hp2 NA18960.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-1874C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405298 | |||||||
chr3:126405419 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.50-1753T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405419 | |||||||
chr3:126405626 | G | C | 54 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0159 others(51): Show |
57 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-1546G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405626 | |||||||
chr3:126405663 | A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0021 a0001c0001t0001g0332 a0001c0001t0001g0333 others(6): Show |
13 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-1493_50-1486dup others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126405663 | ||||||
chr3:126405685 | A | G | 54 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0159 others(51): Show |
57 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-1487A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405685 | |||||||
chr3:126405811 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.50-1361A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405811 | |||||||
chr3:126405848 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.50-1324C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405848 | |||||||
chr3:126405901 | C | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0279 a0001c0001t0001g0303 others(3): Show |
7 | NA18968.hp2 NA18969.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-1271C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405901 | |||||||
chr3:126405976 | C | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.50-1196C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405976 | |||||||
chr3:126406151 | G | T | 1 | a0001c0013t0001g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.50-1021G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406151 | |||||||
chr3:126406189 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.50-983G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406189 | |||||||
chr3:126406208 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
7 | HG00597.hp1 NA18941.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-964C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406208 | |||||||
chr3:126406261 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0126 |
3 | HG00597.hp1 NA18941.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.50-911C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406261 | |||||||
chr3:126406379 | C | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0261 others(5): Show |
9 | HG01081.hp1 HG01928.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.50-793C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406379 | |||||||
chr3:126406419 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.50-753G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406419 | |||||||
chr3:126406457 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.50-715G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406457 | |||||||
chr3:126406623 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0083 others(13): Show |
27 | HG00323.hp1 HG00741.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.50-549G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406623 | |||||||
chr3:126406664 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.50-508C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406664 | |||||||
chr3:126406814 | C | G | 321 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(318): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.50-358C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406814 | |||||||
chr3:126406818 | G | A | 28 | a0001c0001t0001g0030 a0001c0001t0001g0130 a0001c0001t0001g0151 others(25): Show |
35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.50-354G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406818 | |||||||
chr3:126406872 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0257 others(4): Show |
8 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-300A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406872 | |||||||
chr3:126407023 | C | A | 3 | a0001c0001t0001g0172 a0001c0002t0001g0049 a0001c0013t0001g0018 |
4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-149C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126407023 | |||||||
chr3:126407147 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0241 a0001c0001t0002g0242 others(3): Show |
6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-25G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126407147 | |||||||
chr3:126407370 | T | C | 2 | a0001c0002t0001g0337 a0001c0002t0001g0341 |
2 | NA18992.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.130+118T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407370 | |||||||
chr3:126407383 | T | C | 1 | a0001c0002t0001g0050 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.130+131T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407383 | |||||||
chr3:126407429 | T | A | 1 | a0001c0002t0001g0367 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.130+177T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407429 | |||||||
chr3:126407572 | AT | A | 23 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(20): Show |
25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+322delT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126407572 | ||||||
chr3:126407573 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.130+321T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407573 | |||||||
chr3:126407574 | T | G | 23 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(20): Show |
25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+322T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407574 | |||||||
chr3:126407577 | G | T | 23 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(20): Show |
25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+325G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407577 | |||||||
chr3:126407578 | GC | G | 23 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(20): Show |
25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+327delC | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407578 | |||||||
chr3:126407581 | T | C | 23 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(20): Show |
25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+329T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407581 | |||||||
chr3:126407664 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.130+412A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407664 | |||||||
chr3:126407669 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+417C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407669 | |||||||
chr3:126407796 | C | T | 1 | a0001c0002t0001g0368 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.130+544C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407796 | |||||||
chr3:126407941 | T | C | 2 | a0001c0002t0001g0012 a0003c0005t0001g0170 |
3 | HG01106.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130+689T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407941 | |||||||
chr3:126408119 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.130+867G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408119 | |||||||
chr3:126408142 | G | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+890G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408142 | |||||||
chr3:126408192 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130+940C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408192 | |||||||
chr3:126408204 | C | T | 2 | a0004c0007t0001g0019 a0004c0028t0001g0145 |
3 | HG02109.hp2 HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+952C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408204 | |||||||
chr3:126408253 | G | A | 4 | a0001c0008t0001g0013 a0001c0008t0001g0097 a0001c0008t0001g0098 others(1): Show |
5 | NA18944.hp2 NA18974.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+1001G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408253 | |||||||
chr3:126408346 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.130+1094G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408346 | |||||||
chr3:126408473 | C | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0057 others(3): Show |
6 | HG00639.hp2 HG01346.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+1221C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408473 | |||||||
chr3:126408574 | T | C | 1 | a0007c0011t0002g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+1322T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408574 | |||||||
chr3:126408632 | C | T | 1 | a0001c0002t0001g0038 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.130+1380C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408632 | |||||||
chr3:126408705 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.130+1453G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408705 | |||||||
chr3:126408719 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130+1467C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408719 | |||||||
chr3:126408848 | G | A | 5 | a0004c0007t0001g0019 a0004c0007t0001g0135 a0004c0007t0001g0144 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+1596G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408848 | |||||||
chr3:126408935 | C | T | 54 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0159 others(51): Show |
57 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.130+1683C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408935 | |||||||
chr3:126409106 | C | T | 1 | a0002c0004t0001g0185 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.130+1854C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409106 | |||||||
chr3:126409169 | A | T | 2 | a0001c0001t0001g0208 a0012c0020t0001g0089 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.130+1917A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409169 | |||||||
chr3:126409214 | A | T | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130+1962A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409214 | |||||||
chr3:126409253 | C | T | 135 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(132): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.130+2001C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409253 | |||||||
chr3:126409266 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130+2014T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409266 | |||||||
chr3:126409287 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+2035T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409287 | |||||||
chr3:126409382 | T | A | 1 | a0001c0001t0002g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.130+2130T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409382 | |||||||
chr3:126409413 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130+2161G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409413 | |||||||
chr3:126409457 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.130+2205C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409457 | |||||||
chr3:126409516 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.130+2264T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409516 | |||||||
chr3:126409609 | AC | A | 3 | a0001c0001t0001g0088 a0001c0003t0001g0087 a0001c0003t0001g0227 |
3 | HG01243.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.130+2359delC | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126409609 | ||||||
chr3:126409640 | C | G | 1 | a0001c0002t0001g0038 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.130+2388C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409640 | |||||||
chr3:126409644 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.130+2392G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409644 | |||||||
chr3:126409658 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.130+2406C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409658 | |||||||
chr3:126409736 | G | A | 28 | a0001c0001t0001g0030 a0001c0001t0001g0130 a0001c0001t0001g0151 others(25): Show |
35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.130+2484G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409736 | |||||||
chr3:126409785 | T | C | 52 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0159 others(49): Show |
55 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.130+2533T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409785 | |||||||
chr3:126409864 | T | C | 2 | a0001c0001t0001g0325 a0001c0001t0001g0330 |
2 | NA18953.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.130+2612T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409864 | |||||||
chr3:126410005 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.130+2753A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410005 | |||||||
chr3:126410075 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.130+2823C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410075 | |||||||
chr3:126410106 | C | G | 9 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
10 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+2854C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410106 | |||||||
chr3:126410215 | C | T | 10 | a0001c0001t0001g0055 a0001c0001t0001g0200 a0001c0001t0001g0201 others(7): Show |
10 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+2963C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410215 | |||||||
chr3:126410230 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(97): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.130+2978C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410230 | |||||||
chr3:126410273 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.130+3021G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410273 | |||||||
chr3:126410337 | C | T | 54 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0159 others(51): Show |
57 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.130+3085C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410337 | |||||||
chr3:126410490 | C | T | 1 | a0001c0003t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+3238C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410490 | |||||||
chr3:126410560 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0332 a0001c0001t0001g0333 others(6): Show |
13 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+3308G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410560 | |||||||
chr3:126410747 | C | T | 1 | a0001c0001t0001g0023 | 2 | NA18939.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.131-3338C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410747 | |||||||
chr3:126410758 | C | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-3327C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410758 | |||||||
chr3:126410803 | C | T | 193 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(190): Show |
225 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.131-3282C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410803 | |||||||
chr3:126410809 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.131-3276T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410809 | |||||||
chr3:126411015 | G | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(12): Show |
16 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.131-3070G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411015 | |||||||
chr3:126411223 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(20): Show |
27 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.131-2862C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411223 | |||||||
chr3:126411361 | G | GT | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(136): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.131-2698dupT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411361 | G | GTT | 71 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0032 others(68): Show |
84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-2699_131-2698d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411361 | G | GTTT | 9 | a0001c0001t0001g0253 a0001c0001t0001g0328 a0001c0003t0001g0005 others(6): Show |
11 | HG01255.hp2 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-2700_131-2698d others(5): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411361 | G | GTTTT | 19 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0232 others(16): Show |
23 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-2701_131-2698d others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411361 | G | GTTTTT | 6 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02300.hp1 HG02559.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-2702_131-2698d others(7): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411361 | GT | G | 59 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0044 others(56): Show |
63 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.131-2698delT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411361 | GTT | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(22): Show |
30 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.131-2699_131-2698d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411361 | GTTTTTTT others(4): Show |
G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-2708_131-2698d others(13): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | ||||||
chr3:126411524 | T | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0257 others(4): Show |
8 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-2561T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411524 | |||||||
chr3:126411623 | C | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0057 others(2): Show |
5 | HG00639.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-2462C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411623 | |||||||
chr3:126411701 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0083 others(44): Show |
58 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.131-2384T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411701 | |||||||
chr3:126411950 | G | C | 1 | a0012c0020t0001g0089 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.131-2135G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411950 | |||||||
chr3:126411993 | T | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0075 others(20): Show |
27 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.131-2092T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411993 | |||||||
chr3:126412029 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0064 others(54): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-2056T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412029 | |||||||
chr3:126412127 | A | C | 28 | a0001c0001t0001g0045 a0001c0001t0001g0080 a0001c0001t0001g0153 others(25): Show |
28 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-1958A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412127 | |||||||
chr3:126412132 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0140 others(9): Show |
20 | HG00733.hp2 HG02451.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.131-1953C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412132 | |||||||
chr3:126412153 | T | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(30): Show |
38 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.131-1932T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412153 | |||||||
chr3:126412213 | A | G | 1 | a0009c0017t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.131-1872A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412213 | |||||||
chr3:126412244 | T | G | 2 | a0002c0004t0001g0182 a0002c0004t0001g0185 |
2 | HG02080.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.131-1841T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412244 | |||||||
chr3:126412281 | T | A | 210 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.131-1804T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412281 | |||||||
chr3:126412286 | C | T | 184 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(181): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.131-1799C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412286 | |||||||
chr3:126412299 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0002t0001g0202 |
3 | HG01109.hp2 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.131-1786G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412299 | |||||||
chr3:126412396 | C | G | 1 | a0001c0002t0001g0351 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.131-1689C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412396 | |||||||
chr3:126412487 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.131-1598T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412487 | |||||||
chr3:126412611 | C | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.131-1474C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412611 | |||||||
chr3:126412712 | T | C | 34 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0041 others(31): Show |
36 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.131-1373T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412712 | |||||||
chr3:126412844 | T | C | 35 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0041 others(32): Show |
38 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.131-1241T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412844 | |||||||
chr3:126412941 | T | A | 1 | a0001c0001t0001g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.131-1144T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412941 | |||||||
chr3:126413035 | A | G | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0204 others(2): Show |
5 | HG01109.hp2 HG02723.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-1050A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413035 | |||||||
chr3:126413053 | T | G | 16 | a0001c0003t0001g0001 a0001c0003t0001g0005 a0001c0003t0001g0016 others(13): Show |
25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.131-1032T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413053 | |||||||
chr3:126413075 | T | C | 3 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0085 |
3 | HG01346.hp2 HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.131-1010T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413075 | |||||||
chr3:126413188 | T | C | 254 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(251): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.131-897T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413188 | |||||||
chr3:126413301 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0188 others(1): Show |
4 | HG00639.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-784C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413301 | |||||||
chr3:126413339 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-746C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413339 | |||||||
chr3:126413437 | T | C | 248 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(245): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.131-648T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413437 | |||||||
chr3:126413455 | T | G | 5 | a0001c0003t0001g0005 a0001c0003t0001g0051 a0001c0003t0001g0087 others(2): Show |
7 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-630T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413455 | |||||||
chr3:126413552 | C | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0156 others(6): Show |
10 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-533C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413552 | |||||||
chr3:126413851 | C | G | 1 | a0007c0011t0002g0369 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.131-234C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413851 | |||||||
chr3:126413959 | AG | A | 153 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(150): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.131-121delG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126413959 | ||||||
chr3:126413992 | A | G | 34 | a0001c0001t0002g0054 a0001c0003t0001g0001 a0001c0003t0001g0005 others(31): Show |
44 | HG00544.hp1 HG01243.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.131-93A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413992 | |||||||
chr3:126414037 | G | A | 35 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0041 others(32): Show |
37 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.131-48G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126414037 | |||||||
chr3:126414278 | C | G | 1 | a0001c0001t0001g0348 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.225+99C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414278 | |||||||
chr3:126414396 | C | T | 151 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(148): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.225+217C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414396 | |||||||
chr3:126414559 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0088 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.225+380C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414559 | |||||||
chr3:126414560 | A | G | 23 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(20): Show |
25 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.225+381A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414560 | |||||||
chr3:126414644 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0085 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.225+465G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414644 | |||||||
chr3:126414661 | C | T | 1 | a0011c0015t0001g0361 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.225+482C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414661 | |||||||
chr3:126414770 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.225+591C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414770 | |||||||
chr3:126415020 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0001g0356 |
2 | NA19057.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.225+841C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415020 | |||||||
chr3:126415072 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.225+893C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415072 | |||||||
chr3:126415298 | C | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.226-1018C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415298 | |||||||
chr3:126415379 | C | T | 6 | a0005c0009t0001g0046 a0005c0009t0001g0148 a0005c0009t0001g0206 others(3): Show |
6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-937C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415379 | |||||||
chr3:126415413 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.226-903C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415413 | |||||||
chr3:126415434 | C | A | 33 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0020 others(30): Show |
39 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.226-882C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415434 | |||||||
chr3:126415507 | G | A | 1 | a0005c0009t0001g0206 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.226-809G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415507 | |||||||
chr3:126415593 | T | A | 34 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0041 others(31): Show |
36 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.226-723T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415593 | |||||||
chr3:126415633 | G | A | 1 | a0009c0017t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.226-683G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415633 | |||||||
chr3:126415670 | G | A | 8 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0071 others(5): Show |
10 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-646G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415670 | |||||||
chr3:126415675 | C | G | 1 | a0002c0004t0001g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.226-641C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415675 | |||||||
chr3:126415676 | G | C | 1 | a0002c0004t0001g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.226-640G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415676 | |||||||
chr3:126415782 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.226-534T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415782 | |||||||
chr3:126415783 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.226-533C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415783 | |||||||
chr3:126415793 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(242): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.226-523T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415793 | |||||||
chr3:126415862 | A | G | 8 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0071 others(5): Show |
10 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-454A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415862 | |||||||
chr3:126415927 | C | T | 31 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0020 others(28): Show |
37 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.226-389C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415927 | |||||||
chr3:126415944 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.226-372G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415944 | |||||||
chr3:126415963 | G | A | 34 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0041 others(31): Show |
36 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.226-353G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415963 | |||||||
chr3:126416032 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.226-284G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416032 | |||||||
chr3:126416101 | G | C | 1 | a0001c0001t0001g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.226-215G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416101 | |||||||
chr3:126416168 | C | T | 1 | a0009c0017t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.226-148C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416168 | |||||||
chr3:126416179 | T | C | 1 | a0001c0002t0001g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.226-137T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416179 | |||||||
chr3:126416219 | G | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0056 others(3): Show |
8 | HG02258.hp1 HG02486.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-97G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416219 | |||||||
chr3:126416227 | C | CCGCGTCC others(15): Show |
71 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0020 others(68): Show |
80 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.226-81_226-80insCG others(20): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 126416227 | ||||||
chr3:126416235 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.226-81C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416235 | |||||||
chr3:126416256 | G | A | 1 | a0003c0005t0001g0166 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.226-60G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416256 | |||||||
chr3:126416522 | G | T | 87 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0020 others(84): Show |
104 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.418+14G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416522 | |||||||
chr3:126416532 | G | C | 3 | a0007c0011t0002g0169 a0007c0011t0002g0234 a0007c0011t0002g0369 |
3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.418+24G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416532 | |||||||
chr3:126416671 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.418+163G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416671 | |||||||
chr3:126416824 | A | G | 2 | a0001c0002t0001g0049 a0001c0002t0001g0085 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.418+316A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416824 | |||||||
chr3:126416884 | GTTA | G | 17 | a0001c0003t0001g0001 a0001c0003t0001g0005 a0001c0003t0001g0016 others(14): Show |
26 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.418+379_418+381del others(3): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 126416884 | ||||||
chr3:126416889 | T | A | 1 | a0001c0013t0001g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.418+381T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416889 | |||||||
chr3:126416931 | C | T | 87 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0020 others(84): Show |
104 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.418+423C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416931 | |||||||
chr3:126416993 | C | T | 1 | a0001c0002t0001g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.418+485C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416993 | |||||||
chr3:126416994 | T | G | 1 | a0001c0002t0001g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.418+486T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416994 | |||||||
chr3:126416998 | G | A | 3 | a0007c0011t0002g0169 a0007c0011t0002g0234 a0007c0011t0002g0369 |
3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.418+490G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416998 | |||||||
chr3:126416999 | G | T | 1 | a0001c0002t0001g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.418+491G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416999 | |||||||
chr3:126417049 | C | T | 23 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(20): Show |
25 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.418+541C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417049 | |||||||
chr3:126417109 | A | G | 1 | a0002c0004t0001g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.418+601A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417109 | |||||||
chr3:126417110 | G | A | 1 | a0002c0004t0001g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.418+602G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417110 | |||||||
chr3:126417279 | C | T | 1 | a0005c0009t0002g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.418+771C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417279 | |||||||
chr3:126417291 | T | TAAGA | 88 | a0001c0001t0001g0342 a0001c0002t0001g0010 a0001c0002t0001g0012 others(85): Show |
105 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.418+785_418+788dup others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 126417291 | ||||||
chr3:126417315 | G | A | 1 | a0001c0018t0001g0319 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.418+807G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417315 | |||||||
chr3:126417329 | G | A | 35 | a0001c0001t0001g0342 a0001c0002t0001g0038 a0001c0002t0001g0040 others(32): Show |
37 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.418+821G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417329 | |||||||
chr3:126417365 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.418+857G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417365 | |||||||
chr3:126417566 | G | A | 1 | a0001c0013t0001g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.419-892G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417566 | |||||||
chr3:126417616 | G | A | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-842G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417616 | |||||||
chr3:126417633 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.419-825G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417633 | |||||||
chr3:126417636 | G | A | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(105): Show |
126 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.419-822G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417636 | |||||||
chr3:126417638 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.419-820C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417638 | |||||||
chr3:126417651 | C | G | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-807C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417651 | |||||||
chr3:126417659 | G | A | 8 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0071 others(5): Show |
10 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.419-799G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417659 | |||||||
chr3:126417693 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.419-765C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417693 | |||||||
chr3:126417729 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.419-729C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417729 | |||||||
chr3:126417730 | G | A | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-728G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417730 | |||||||
chr3:126417753 | G | C | 1 | a0001c0006t0001g0264 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.419-705G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417753 | |||||||
chr3:126417881 | C | T | 1 | a0012c0020t0001g0089 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.419-577C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417881 | |||||||
chr3:126417906 | C | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0140 others(6): Show |
10 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.419-552C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417906 | |||||||
chr3:126417927 | A | C | 89 | a0001c0001t0001g0023 a0001c0001t0001g0342 a0001c0002t0001g0010 others(86): Show |
107 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.419-531A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417927 | |||||||
chr3:126418199 | G | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(104): Show |
124 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.419-259G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418199 | |||||||
chr3:126418235 | G | C | 222 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(219): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.419-223G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418235 | |||||||
chr3:126418237 | G | A | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-221G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418237 | |||||||
chr3:126418418 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.419-40G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418418 | |||||||
chr3:126418427 | G | A | 3 | a0007c0011t0002g0169 a0007c0011t0002g0234 a0007c0011t0002g0369 |
3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.419-31G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418427 | |||||||
chr3:126418790 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0188 others(1): Show |
4 | HG00639.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+16C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418790 | |||||||
chr3:126418791 | G | A | 18 | a0001c0001t0001g0168 a0001c0003t0001g0001 a0001c0003t0001g0005 others(15): Show |
27 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.650+17G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418791 | |||||||
chr3:126418834 | C | T | 3 | a0007c0011t0002g0169 a0007c0011t0002g0234 a0007c0011t0002g0369 |
3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.650+60C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418834 | |||||||
chr3:126418936 | A | C | 1 | a0001c0001t0001g0313 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.651-140A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418936 | |||||||
chr3:126418949 | T | A | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.651-127T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418949 | |||||||
chr3:126419019 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.651-57A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126419019 | |||||||
chr3:126419198 | C | T | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.731+42C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/16 | chr3 | 126419198 | |||||||
chr3:126419472 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.732-165G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/16 | chr3 | 126419472 | |||||||
chr3:126419844 | C | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0114 a0001c0001t0001g0314 others(2): Show |
5 | HG00621.hp1 HG01993.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+26C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 9/16 | chr3 | 126419844 | |||||||
chr3:126419935 | T | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(276): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.914-45T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 9/16 | chr3 | 126419935 | |||||||
chr3:126420043 | G | A | 1 | a0001c0006t0001g0263 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.955+22G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 10/16 | chr3 | 126420043 | |||||||
chr3:126420046 | G | T | 95 | a0001c0001t0001g0153 a0001c0001t0002g0197 a0001c0002t0001g0010 others(92): Show |
112 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.955+25G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 10/16 | chr3 | 126420046 | |||||||
chr3:126420077 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.956-26G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 10/16 | chr3 | 126420077 | |||||||
chr3:126420241 | CG | C | 23 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(20): Show |
25 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1082+15delG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 126420241 | ||||||
chr3:126420243 | G | C | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1082+14G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420243 | |||||||
chr3:126420275 | G | C | 1 | a0001c0001t0001g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1082+46G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420275 | |||||||
chr3:126420461 | G | C | 2 | a0001c0013t0001g0018 a0009c0017t0001g0147 |
3 | HG02895.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1082+232G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420461 | |||||||
chr3:126420557 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1082+328T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420557 | |||||||
chr3:126420777 | G | A | 96 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0002g0197 others(93): Show |
115 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1082+548G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420777 | |||||||
chr3:126420836 | A | G | 16 | a0001c0003t0001g0001 a0001c0003t0001g0005 a0001c0003t0001g0016 others(13): Show |
25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1082+607A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420836 | |||||||
chr3:126420844 | C | CTTATTGG others(8): Show |
95 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0002g0197 others(92): Show |
114 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1082+615_1082+616i others(17): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420844 | |||||||
chr3:126420932 | G | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0236 others(2): Show |
8 | HG00280.hp2 HG00741.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082+703G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420932 | |||||||
chr3:126420998 | T | C | 14 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0039 others(11): Show |
17 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1082+769T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420998 | |||||||
chr3:126421112 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1082+883C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421112 | |||||||
chr3:126421127 | C | T | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
111 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1082+898C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421127 | |||||||
chr3:126421185 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1082+956G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421185 | |||||||
chr3:126421227 | C | G | 2 | a0001c0002t0001g0049 a0001c0002t0001g0085 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1082+998C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421227 | |||||||
chr3:126421330 | T | C | 1 | a0012c0020t0001g0089 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1082+1101T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421330 | |||||||
chr3:126421405 | C | T | 1 | a0001c0001t0001g0334 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1082+1176C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421405 | |||||||
chr3:126421489 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0304 |
4 | NA18948.hp1 NA18993.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082+1260C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421489 | |||||||
chr3:126421493 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1082+1264G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421493 | |||||||
chr3:126421583 | G | A | 1 | a0001c0003t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1082+1354G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421583 | |||||||
chr3:126421741 | G | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1082+1512G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421741 | |||||||
chr3:126421811 | C | A | 123 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0030 others(120): Show |
137 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1083-1514C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421811 | |||||||
chr3:126421864 | A | G | 2 | a0001c0002t0001g0048 a0001c0025t0001g0059 |
2 | HG01346.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1083-1461A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421864 | |||||||
chr3:126421868 | C | T | 4 | a0004c0007t0001g0019 a0004c0007t0001g0135 a0004c0007t0001g0254 others(1): Show |
5 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083-1457C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421868 | |||||||
chr3:126421921 | A | G | 7 | a0001c0001t0002g0054 a0001c0002t0001g0202 a0001c0013t0001g0018 others(4): Show |
9 | HG01109.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083-1404A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421921 | |||||||
chr3:126422036 | G | C | 1 | a0002c0004t0001g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1083-1289G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422036 | |||||||
chr3:126422038 | T | C | 2 | a0001c0002t0001g0049 a0001c0002t0001g0085 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1083-1287T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422038 | |||||||
chr3:126422141 | C | A | 1 | a0001c0013t0001g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1083-1184C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422141 | |||||||
chr3:126422313 | G | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(91): Show |
111 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1083-1012G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422313 | |||||||
chr3:126422330 | T | C | 12 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(9): Show |
12 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083-995T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422330 | |||||||
chr3:126422332 | T | A | 1 | a0009c0017t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1083-993T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422332 | |||||||
chr3:126422342 | C | T | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1083-983C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422342 | |||||||
chr3:126422365 | C | G | 1 | a0009c0017t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1083-960C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422365 | |||||||
chr3:126422366 | C | G | 1 | a0009c0017t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1083-959C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422366 | |||||||
chr3:126422437 | A | G | 1 | a0001c0013t0001g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1083-888A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422437 | |||||||
chr3:126422488 | GC | G | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(136): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083-829delC | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 126422488 | ||||||
chr3:126422490 | C | A | 1 | a0005c0024t0002g0199 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1083-835C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422490 | |||||||
chr3:126422490 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1083-835C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422490 | |||||||
chr3:126422505 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0146 |
3 | HG02135.hp1 HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1083-820C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422505 | |||||||
chr3:126422519 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1083-806G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422519 | |||||||
chr3:126422592 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0293 |
2 | HG00099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1083-733C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422592 | |||||||
chr3:126422593 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1083-732G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422593 | |||||||
chr3:126422610 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1083-715G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422610 | |||||||
chr3:126422827 | G | A | 7 | a0003c0005t0001g0002 a0003c0005t0001g0086 a0003c0005t0001g0152 others(4): Show |
10 | HG00140.hp1 HG00639.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083-498G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422827 | |||||||
chr3:126422860 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0330 |
2 | NA18953.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1083-465C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422860 | |||||||
chr3:126423014 | A | G | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(136): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083-311A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423014 | |||||||
chr3:126423018 | G | A | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1083-307G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423018 | |||||||
chr3:126423050 | C | A | 32 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(29): Show |
34 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1083-275C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423050 | |||||||
chr3:126423068 | G | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(10): Show |
15 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1083-257G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423068 | |||||||
chr3:126423202 | G | T | 1 | a0002c0004t0001g0218 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1083-123G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423202 | |||||||
chr3:126423320 | C | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0071 a0001c0002t0001g0142 others(2): Show |
6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1083-5C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423320 | |||||||
chr3:126423463 | C | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1135-30C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 12/16 | chr3 | 126423463 | |||||||
chr3:126423653 | T | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): Show |
134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1286+9T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423653 | |||||||
chr3:126423682 | G | A | 1 | a0006c0010t0001g0022 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1286+38G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423682 | |||||||
chr3:126423740 | C | T | 8 | a0001c0002t0001g0012 a0001c0002t0001g0082 a0001c0002t0001g0238 others(5): Show |
11 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1286+96C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423740 | |||||||
chr3:126423745 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1286+101G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423745 | |||||||
chr3:126423755 | C | T | 13 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(10): Show |
13 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1286+111C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423755 | |||||||
chr3:126423839 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1286+195G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423839 | |||||||
chr3:126423852 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1286+208C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423852 | |||||||
chr3:126423857 | G | A | 7 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0071 others(4): Show |
9 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286+213G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423857 | |||||||
chr3:126423974 | A | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1286+330A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423974 | |||||||
chr3:126423983 | G | A | 9 | a0001c0001t0001g0275 a0001c0001t0001g0309 a0001c0001t0001g0310 others(6): Show |
9 | HG00673.hp1 HG02040.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286+339G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423983 | |||||||
chr3:126423990 | C | A | 1 | a0001c0002t0001g0251 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1286+346C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423990 | |||||||
chr3:126423998 | A | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1286+354A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423998 | |||||||
chr3:126424012 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1286+368G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424012 | |||||||
chr3:126424028 | G | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1286+384G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424028 | |||||||
chr3:126424182 | G | A | 1 | a0001c0006t0001g0263 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1286+538G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424182 | |||||||
chr3:126424182 | G | C | 23 | a0001c0002t0001g0038 a0001c0002t0001g0092 a0001c0002t0001g0101 others(20): Show |
24 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(21): Show |
intron_variant | MODIFIER | c.1286+538G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424182 | |||||||
chr3:126424183 | G | C | 1 | a0001c0002t0001g0308 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1286+539G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424183 | |||||||
chr3:126424211 | C | T | 8 | a0001c0002t0001g0012 a0001c0002t0001g0082 a0001c0002t0001g0238 others(5): Show |
11 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1286+567C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424211 | |||||||
chr3:126424442 | A | G | 3 | a0007c0011t0002g0169 a0007c0011t0002g0234 a0007c0011t0002g0369 |
3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1286+798A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424442 | |||||||
chr3:126424454 | A | G | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+810A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424454 | |||||||
chr3:126424647 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1286+1003G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424647 | |||||||
chr3:126424765 | A | G | 2 | a0001c0001t0001g0162 a0009c0017t0001g0147 |
2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1286+1121A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424765 | |||||||
chr3:126424808 | G | C | 2 | a0001c0002t0001g0084 a0001c0013t0001g0018 |
3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1286+1164G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424808 | |||||||
chr3:126424884 | G | A | 222 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(219): Show |
259 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1286+1240G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424884 | |||||||
chr3:126424924 | A | T | 1 | a0001c0002t0001g0308 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1286+1280A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424924 | |||||||
chr3:126425171 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0304 |
4 | NA18948.hp1 NA18993.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+1527T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425171 | |||||||
chr3:126425177 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0146 |
3 | HG02135.hp1 HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1286+1533C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425177 | |||||||
chr3:126425182 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1286+1538G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425182 | |||||||
chr3:126425192 | T | C | 1 | a0001c0008t0001g0097 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1286+1548T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425192 | |||||||
chr3:126425330 | A | G | 1 | a0001c0025t0001g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1286+1686A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425330 | |||||||
chr3:126425473 | A | C | 8 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(5): Show |
8 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+1829A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425473 | |||||||
chr3:126425519 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1286+1875A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425519 | |||||||
chr3:126425549 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1286+1905G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425549 | |||||||
chr3:126425602 | C | A | 25 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(22): Show |
27 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1286+1958C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425602 | |||||||
chr3:126425641 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02083.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1286+1997C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425641 | |||||||
chr3:126425648 | T | C | 12 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0203 others(9): Show |
12 | HG01109.hp2 HG02145.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1286+2004T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425648 | |||||||
chr3:126425774 | C | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+2130C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425774 | |||||||
chr3:126425789 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG01109.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+2145C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425789 | |||||||
chr3:126425851 | A | G | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(108): Show |
127 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1286+2207A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425851 | |||||||
chr3:126425903 | C | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+2259C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425903 | |||||||
chr3:126425934 | A | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+2290A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425934 | |||||||
chr3:126425967 | A | G | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1286+2323A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425967 | |||||||
chr3:126426013 | G | T | 7 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0071 others(4): Show |
9 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286+2369G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426013 | |||||||
chr3:126426028 | T | C | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG00735.hp1 HG01074.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+2384T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426028 | |||||||
chr3:126426217 | C | A | 8 | a0001c0002t0001g0012 a0001c0002t0001g0082 a0001c0002t0001g0238 others(5): Show |
11 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1286+2573C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426217 | |||||||
chr3:126426280 | T | C | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1286+2636T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426280 | |||||||
chr3:126426454 | T | TA | 29 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0188 others(26): Show |
30 | HG00408.hp2 HG00544.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1286+2825dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126426454 | ||||||
chr3:126426454 | T | TAA | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(81): Show |
99 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1286+2824_1286+282 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126426454 | ||||||
chr3:126426454 | TA | T | 31 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0002t0001g0038 others(28): Show |
34 | HG01243.hp2 HG01255.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.1286+2825delA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126426454 | ||||||
chr3:126426477 | T | C | 16 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(13): Show |
17 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1286+2833T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426477 | |||||||
chr3:126426578 | C | T | 4 | a0004c0007t0001g0019 a0004c0007t0001g0135 a0004c0007t0001g0254 others(1): Show |
5 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+2934C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426578 | |||||||
chr3:126426682 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1286+3038G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426682 | |||||||
chr3:126426705 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1286+3061G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426705 | |||||||
chr3:126426765 | A | G | 24 | a0001c0002t0001g0038 a0001c0002t0001g0092 a0001c0002t0001g0101 others(21): Show |
25 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1286+3121A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426765 | |||||||
chr3:126426833 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1286+3189T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426833 | |||||||
chr3:126426977 | G | A | 15 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(12): Show |
16 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1286+3333G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426977 | |||||||
chr3:126427029 | T | C | 1 | a0004c0007t0001g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1286+3385T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427029 | |||||||
chr3:126427092 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1286+3448A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427092 | |||||||
chr3:126427162 | T | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0180 a0001c0001t0001g0296 others(3): Show |
6 | HG02071.hp2 NA18940.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+3518T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427162 | |||||||
chr3:126427317 | G | A | 2 | a0003c0005t0001g0086 a0003c0005t0001g0235 |
2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1286+3673G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427317 | |||||||
chr3:126427326 | T | C | 8 | a0001c0002t0001g0012 a0001c0002t0001g0082 a0001c0002t0001g0238 others(5): Show |
11 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1286+3682T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427326 | |||||||
chr3:126427472 | GGTGTCTG others(19): Show |
G | 1 | a0001c0001t0001g0065 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1286+3836_1286+386 others(30): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126427472 | ||||||
chr3:126427543 | C | T | 1 | a0001c0003t0001g0255 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+3899C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427543 | |||||||
chr3:126427776 | TTTTAA | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0203 a0001c0002t0001g0202 |
3 | HG02572.hp1 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+4136_1286+414 others(9): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126427776 | ||||||
chr3:126427935 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+4291G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427935 | |||||||
chr3:126428023 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0154 others(1): Show |
4 | HG00639.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+4379G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428023 | |||||||
chr3:126428052 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1286+4408C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428052 | |||||||
chr3:126428054 | T | C | 220 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(217): Show |
257 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1286+4410T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428054 | |||||||
chr3:126428156 | A | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+4512A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428156 | |||||||
chr3:126428364 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-4705G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428364 | |||||||
chr3:126428368 | TAAAG | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-4699_1287-469 others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126428368 | ||||||
chr3:126428661 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1287-4408T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428661 | |||||||
chr3:126428699 | A | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01109.hp2 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287-4370A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428699 | |||||||
chr3:126428744 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1287-4325C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428744 | |||||||
chr3:126428881 | T | C | 1 | a0001c0002t0001g0367 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1287-4188T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428881 | |||||||
chr3:126429065 | T | C | 220 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(217): Show |
257 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1287-4004T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429065 | |||||||
chr3:126429066 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-4003G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429066 | |||||||
chr3:126429098 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1287-3971G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429098 | |||||||
chr3:126429107 | C | CA | 23 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0096 others(20): Show |
24 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1287-3935dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CA | C | 11 | a0001c0001t0001g0057 a0001c0001t0001g0118 a0001c0001t0001g0126 others(8): Show |
11 | HG00639.hp1 HG01891.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287-3935delA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CAA | C | 33 | a0001c0001t0001g0055 a0001c0001t0001g0205 a0001c0001t0001g0229 others(30): Show |
42 | HG00544.hp1 HG01891.hp1 HG02080.hp2 others(39): Show |
intron_variant | MODIFIER | c.1287-3936_1287-393 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CAAA | C | 59 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0032 others(56): Show |
68 | HG00280.hp1 HG01070.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.1287-3937_1287-393 others(7): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CAAAA | C | 16 | a0001c0001t0001g0031 a0001c0001t0001g0273 a0001c0002t0001g0039 others(13): Show |
18 | HG00408.hp2 HG01256.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.1287-3938_1287-393 others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CAAAAA | C | 15 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(12): Show |
16 | HG00733.hp1 HG01109.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.1287-3939_1287-393 others(9): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0314 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1287-3944_1287-393 others(14): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1287-3945_1287-393 others(15): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429107 | CAAAAAAA others(9): Show |
C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-3950_1287-393 others(20): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | ||||||
chr3:126429129 | A | G | 1 | a0001c0001t0001g0350 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1287-3940A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429129 | |||||||
chr3:126429162 | G | C | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-3907G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429162 | |||||||
chr3:126429223 | T | C | 2 | a0001c0001t0001g0162 a0009c0017t0001g0147 |
2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-3846T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429223 | |||||||
chr3:126429253 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-3816T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429253 | |||||||
chr3:126429455 | T | C | 2 | a0001c0001t0001g0162 a0009c0017t0001g0147 |
2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-3614T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429455 | |||||||
chr3:126429622 | G | GT | 282 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1287-3436dupT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429622 | ||||||
chr3:126429622 | G | GTT | 26 | a0001c0001t0001g0091 a0001c0001t0001g0304 a0001c0001t0001g0350 others(23): Show |
27 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1287-3437_1287-343 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429622 | ||||||
chr3:126429765 | T | TTATACTT others(3): Show |
1 | a0001c0001t0001g0365 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1287-3300_1287-329 others(14): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429765 | ||||||
chr3:126429785 | G | A | 2 | a0001c0001t0001g0183 a0015c0019t0001g0174 |
2 | NA19011.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1287-3284G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429785 | |||||||
chr3:126429811 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1287-3258T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429811 | |||||||
chr3:126429909 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-3160T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429909 | |||||||
chr3:126429942 | C | A | 16 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(13): Show |
17 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1287-3127C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429942 | |||||||
chr3:126430009 | T | C | 1 | a0002c0004t0001g0221 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1287-3060T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430009 | |||||||
chr3:126430031 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-3038C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430031 | |||||||
chr3:126430043 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1287-3026G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430043 | |||||||
chr3:126430050 | T | A | 3 | a0001c0002t0001g0012 a0001c0002t0001g0082 a0001c0002t0001g0238 |
4 | HG00280.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287-3019T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430050 | |||||||
chr3:126430079 | C | A | 1 | a0001c0001t0001g0353 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1287-2990C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430079 | |||||||
chr3:126430157 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-2912G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430157 | |||||||
chr3:126430232 | T | TTAAG | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-2835_1287-283 others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126430232 | ||||||
chr3:126430450 | A | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-2619A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430450 | |||||||
chr3:126430763 | T | TG | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(104): Show |
123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1287-2303dupG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126430763 | ||||||
chr3:126430767 | T | G | 9 | a0001c0001t0001g0362 a0001c0002t0001g0049 a0001c0002t0001g0085 others(6): Show |
11 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287-2302T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430767 | |||||||
chr3:126430862 | T | C | 49 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(46): Show |
52 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.1287-2207T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430862 | |||||||
chr3:126430912 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1287-2157A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430912 | |||||||
chr3:126430963 | A | C | 8 | a0001c0002t0001g0012 a0001c0002t0001g0082 a0001c0002t0001g0238 others(5): Show |
11 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287-2106A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430963 | |||||||
chr3:126430964 | T | C | 9 | a0001c0001t0001g0080 a0001c0001t0001g0180 a0001c0001t0001g0296 others(6): Show |
9 | HG02040.hp1 HG02071.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-2105T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430964 | |||||||
chr3:126431011 | C | T | 1 | a0001c0003t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1287-2058C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431011 | |||||||
chr3:126431101 | G | C | 2 | a0001c0001t0001g0162 a0009c0017t0001g0147 |
2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-1968G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431101 | |||||||
chr3:126431105 | C | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(87): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1287-1964C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431105 | |||||||
chr3:126431385 | C | A | 1 | a0001c0002t0001g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1287-1684C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431385 | |||||||
chr3:126431419 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1287-1650C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431419 | |||||||
chr3:126431498 | A | G | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-1571A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431498 | |||||||
chr3:126431529 | C | T | 7 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0071 others(4): Show |
9 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287-1540C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431529 | |||||||
chr3:126431683 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG01192.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1287-1386G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431683 | |||||||
chr3:126431687 | A | C | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-1382A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431687 | |||||||
chr3:126431740 | T | TTC | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-1328_1287-132 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126431740 | ||||||
chr3:126431794 | C | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1287-1275C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431794 | |||||||
chr3:126431886 | ACT | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01169.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1287-1180_1287-117 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126431886 | ||||||
chr3:126432007 | G | A | 17 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(14): Show |
18 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1287-1062G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432007 | |||||||
chr3:126432052 | A | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-1017A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432052 | |||||||
chr3:126432077 | G | A | 1 | a0001c0001t0005g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1287-992G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432077 | |||||||
chr3:126432077 | G | C | 2 | a0001c0002t0001g0049 a0001c0002t0001g0085 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1287-992G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432077 | |||||||
chr3:126432085 | C | T | 2 | a0001c0002t0001g0084 a0001c0013t0001g0018 |
3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1287-984C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432085 | |||||||
chr3:126432136 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-933G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432136 | |||||||
chr3:126432187 | G | A | 24 | a0001c0002t0001g0038 a0001c0002t0001g0092 a0001c0002t0001g0101 others(21): Show |
25 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1287-882G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432187 | |||||||
chr3:126432232 | T | C | 17 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(14): Show |
18 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1287-837T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432232 | |||||||
chr3:126432266 | G | A | 2 | a0001c0001t0001g0162 a0009c0017t0001g0147 |
2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-803G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432266 | |||||||
chr3:126432282 | C | CA | 90 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(87): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1287-765dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | ||||||
chr3:126432282 | C | CAA | 14 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0143 others(11): Show |
15 | HG00735.hp1 HG01258.hp1 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.1287-766_1287-765d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | ||||||
chr3:126432282 | CA | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(129): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1287-765delA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | ||||||
chr3:126432282 | CAA | C | 9 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0335 others(6): Show |
11 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-766_1287-765d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | ||||||
chr3:126432348 | T | C | 16 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(13): Show |
17 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1287-721T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432348 | |||||||
chr3:126432429 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-640G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432429 | |||||||
chr3:126432518 | G | T | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-551G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432518 | |||||||
chr3:126432536 | ATGC | A | 25 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(22): Show |
27 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1287-529_1287-527d others(5): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432536 | ||||||
chr3:126432630 | T | TCAGGGTA others(1): Show |
49 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(46): Show |
52 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.1287-438_1287-431d others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432630 | ||||||
chr3:126432632 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1287-437A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432632 | |||||||
chr3:126432693 | A | G | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-376A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432693 | |||||||
chr3:126432788 | CTT | C | 5 | a0001c0003t0001g0005 a0001c0003t0001g0051 a0001c0003t0001g0087 others(2): Show |
7 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-280_1287-279d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432788 | |||||||
chr3:126432837 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(88): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1287-232C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432837 | |||||||
chr3:126432954 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-115T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432954 | |||||||
chr3:126433051 | G | A | 10 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(7): Show |
10 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1287-18G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126433051 | |||||||
chr3:126433281 | G | A | 30 | a0001c0001t0002g0054 a0001c0003t0001g0001 a0001c0003t0001g0016 others(27): Show |
38 | HG00544.hp1 HG01891.hp1 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.1422+77G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433281 | |||||||
chr3:126433308 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1422+104C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433308 | |||||||
chr3:126433487 | G | T | 6 | a0001c0001t0001g0293 a0001c0001t0001g0318 a0001c0003t0001g0005 others(3): Show |
8 | HG00099.hp1 HG00140.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1422+283G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433487 | |||||||
chr3:126433499 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1422+295C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433499 | |||||||
chr3:126433541 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1422+337G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433541 | |||||||
chr3:126433623 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1422+419G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433623 | |||||||
chr3:126433631 | C | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1422+427C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433631 | |||||||
chr3:126433674 | C | T | 17 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0241 others(14): Show |
18 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1422+470C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433674 | |||||||
chr3:126433675 | AG | A | 3 | a0007c0011t0002g0169 a0007c0011t0002g0234 a0007c0011t0002g0369 |
3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1422+473delG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 126433675 | ||||||
chr3:126433688 | A | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02083.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1422+484A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433688 | |||||||
chr3:126433764 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1423-412C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433764 | |||||||
chr3:126433821 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1423-355C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433821 | |||||||
chr3:126433925 | C | T | 5 | a0004c0007t0001g0019 a0004c0007t0001g0135 a0004c0007t0001g0144 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1423-251C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433925 | |||||||
chr3:126433986 | G | A | 1 | a0009c0017t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1423-190G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433986 | |||||||
chr3:126434001 | C | T | 2 | a0001c0001t0001g0162 a0009c0017t0001g0147 |
2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1423-175C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126434001 | |||||||
chr3:126434137 | C | T | 24 | a0001c0002t0001g0038 a0001c0002t0001g0092 a0001c0002t0001g0101 others(21): Show |
25 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1423-39C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126434137 | |||||||
chr3:126434174 | A | C | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1423-2A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126434174 | |||||||
chr3:126434416 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(8): Show |
13 | HG01070.hp2 HG01071.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1628+35C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434416 | |||||||
chr3:126434467 | C | T | 29 | a0001c0001t0002g0054 a0001c0003t0001g0001 a0001c0003t0001g0016 others(26): Show |
37 | HG00544.hp1 HG01891.hp1 HG02080.hp2 others(34): Show |
intron_variant | MODIFIER | c.1628+86C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434467 | |||||||
chr3:126434518 | T | C | 132 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(129): Show |
153 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1628+137T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434518 | |||||||
chr3:126434600 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1628+219G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434600 | |||||||
chr3:126434734 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0157 others(9): Show |
15 | HG00408.hp2 HG01256.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1628+353C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434734 | |||||||
chr3:126434774 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1628+393G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434774 | |||||||
chr3:126434795 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1628+414G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434795 | |||||||
chr3:126434858 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1628+477G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434858 | |||||||
chr3:126434921 | G | T | 1 | a0011c0029t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1628+540G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434921 | |||||||
chr3:126434949 | C | G | 39 | a0001c0001t0002g0054 a0001c0002t0001g0049 a0001c0002t0001g0082 others(36): Show |
49 | HG00280.hp1 HG00544.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.1628+568C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434949 | |||||||
chr3:126434949 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1628+568C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434949 | |||||||
chr3:126435004 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0085 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1629-555G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435004 | |||||||
chr3:126435034 | C | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0071 a0001c0002t0001g0142 others(2): Show |
6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1629-525C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435034 | |||||||
chr3:126435079 | A | G | 7 | a0001c0001t0002g0027 a0001c0001t0002g0241 a0001c0001t0002g0242 others(4): Show |
7 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1629-480A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435079 | |||||||
chr3:126435101 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1629-458C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435101 | |||||||
chr3:126435151 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1629-408G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435151 | |||||||
chr3:126435313 | A | G | 6 | a0001c0001t0001g0198 a0001c0001t0001g0203 a0001c0003t0001g0028 others(3): Show |
8 | HG02145.hp2 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629-246A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435313 | |||||||
chr3:126435358 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1629-201C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435358 | |||||||
chr3:126435391 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0304 a0001c0001t0001g0336 others(2): Show |
7 | HG00423.hp2 NA18948.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1629-168G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435391 | |||||||
chr3:126435475 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1629-84C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435475 | |||||||
chr3:126435476 | G | A | 25 | a0001c0001t0001g0024 a0001c0001t0001g0220 a0001c0002t0001g0038 others(22): Show |
27 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(24): Show |
intron_variant | MODIFIER | c.1629-83G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435476 | |||||||
chr3:126435488 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1629-71G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435488 | |||||||
chr3:126435538 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1629-21A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435538 | |||||||
chr3:126435554 | C | A | 23 | a0001c0002t0001g0038 a0001c0002t0001g0101 a0001c0002t0001g0104 others(20): Show |
24 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1629-5C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435554 | |||||||
chr3:126435698 | G | C | 1 | a0001c0001t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1722+46G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126435698 | |||||||
chr3:126435791 | G | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(95): Show |
120 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1722+139G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126435791 | |||||||
chr3:126435979 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1723-312C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126435979 | |||||||
chr3:126436015 | C | A | 2 | a0002c0004t0001g0149 a0006c0010t0001g0022 |
3 | HG01109.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1723-276C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126436015 | |||||||
chr3:126436162 | C | G | 6 | a0002c0004t0001g0149 a0004c0007t0001g0019 a0004c0007t0001g0135 others(3): Show |
8 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1723-129C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126436162 | |||||||
chr3:126436173 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0056 others(11): Show |
16 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1723-118G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126436173 |