Item | Value |
---|---|
geneid | 57501 |
ensemblid | ENSG00000114656.13 |
hgncid | 29231 |
symbol | CFAP92 |
name | cilia and flagella associated protein 92 (putative) |
refseq_nuc | NM_001394090.1 |
refseq_prot | NP_001381019.1 |
ensembl_nuc | ENST00000645291.3 |
ensembl_prot | ENSP00000496592.2 |
mane_status | MANE Select |
chr | chr3 |
start | 128909873 |
end | 128994076 |
strand | - |
ver | v1.2 |
region | chr3:128909873-128994076 |
region5000 | chr3:128904873-128999076 |
regionname0 | CFAP92_chr3_128909873_128994076 |
regionname5000 | CFAP92_chr3_128904873_128999076 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1104 | 296 | 64 | 68 | 118 | 15 | 30 | 87 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0002 | 0/0 | 1104 | 23 | 9 | 0 | 7 | 0 | 7 | 5 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0003 | 0/0 | 1104 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0004 | 0/0 | 1103 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1098): Show |
chr3 | 128904873 | 128999076 |
a0005 | 0/0 | 1104 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0006 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0007 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0008 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0009 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0010 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0011 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0012 | 0/0 | 505 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(500): Show |
chr3 | 128904873 | 128999076 |
a0013 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0014 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0015 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0016 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
a0017 | 0/1 | 1104 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | MSLHA others(1099): Show |
chr3 | 128904873 | 128999076 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3312 | 285 | 55 | 67 | 117 | 15 | 30 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0001c0003 | 0/0 | 3312 | 9 | 8 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0001c0014 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0001c0016 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0002c0002 | 0/0 | 3312 | 23 | 9 | 0 | 7 | 0 | 7 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0003c0004 | 0/0 | 3312 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0004c0006 | 0/0 | 3309 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3304): Show |
chr3 | 128904873 | 128999076 | ||
a0004c0021 | 0/0 | 3309 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3304): Show |
chr3 | 128904873 | 128999076 | ||
a0005c0005 | 0/0 | 3312 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0006c0017 | 0/0 | 3312 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0007c0012 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0008c0020 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0009c0013 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0010c0008 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0011c0009 | 0/0 | 3312 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0012c0018 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(2402): Show |
chr3 | 128904873 | 128999076 | ||
a0013c0010 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0014c0019 | 0/0 | 3312 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0015c0015 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0016c0007 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 | ||
a0017c0011 | 0/1 | 3312 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | ATGTC others(3307): Show |
chr3 | 128904873 | 128999076 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3870 | 268 | 47 | 61 | 116 | 14 | 29 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0001t0003 | 0/0 | 3870 | 7 | 6 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0001t0004 | 0/0 | 3867 | 5 | 0 | 4 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3862): Show |
chr3 | 128904873 | 128999076 |
a0001c0001t0005 | 0/0 | 3870 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0001t0006 | 0/0 | 3870 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0001t0007 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0001t0008 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0003t0001 | 0/0 | 3870 | 9 | 8 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0014t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0001c0016t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0002c0002t0002 | 0/0 | 3870 | 23 | 9 | 0 | 7 | 0 | 7 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0003c0004t0002 | 0/0 | 3870 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0004c0006t0001 | 0/0 | 3867 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3862): Show |
chr3 | 128904873 | 128999076 |
a0004c0021t0001 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3862): Show |
chr3 | 128904873 | 128999076 |
a0005c0005t0001 | 0/0 | 3870 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0006c0017t0001 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0007c0012t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0008c0020t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0009c0013t0002 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0010c0008t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0011c0009t0001 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0012c0018t0001 | 0/0 | 2965 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(2960): Show |
chr3 | 128904873 | 128999076 |
a0013c0010t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0014c0019t0001 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0015c0015t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0016c0007t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
a0017c0011t0001 | 0/1 | 3870 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | AGTCT others(3865): Show |
chr3 | 128904873 | 128999076 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0001t0008g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0014t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0001c0016t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0003c0004t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0003c0004t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0003c0004t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0003c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0003c0004t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0003c0004t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0004c0006t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0004c0006t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0004c0021t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0005c0005t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0005c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0006c0017t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0007c0012t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0008c0020t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0009c0013t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0010c0008t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0011c0009t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0012c0018t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0013c0010t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0014c0019t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0015c0015t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0016c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
a0017c0011t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00323 | hp1 | a0006 | c0017 | t0001 | g0176 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0211 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00642 | hp1 | a0004 | c0006 | t0001 | g0329 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0273 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00673 | hp2 | a0001 | c0014 | t0001 | g0065 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0093 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01109 | hp2 | a0005 | c0005 | t0001 | g0014 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0274 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0209 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01891 | hp1 | a0004 | c0021 | t0001 | g0328 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0321 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0301 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02135 | hp1 | a0007 | c0012 | t0001 | g0054 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02145 | hp2 | a0008 | c0020 | t0001 | g0110 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02258 | hp1 | a0003 | c0004 | t0002 | g0182 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0323 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0333 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02451 | hp1 | a0001 | c0016 | t0001 | g0198 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0316 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02572 | hp2 | a0009 | c0013 | t0002 | g0143 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0206 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02622 | hp2 | a0003 | c0004 | t0002 | g0185 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0315 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02698 | hp2 | a0001 | c0001 | t0008 | g0334 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02717 | hp2 | a0010 | c0008 | t0001 | g0048 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0213 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0318 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02965 | hp2 | a0004 | c0006 | t0001 | g0330 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02970 | hp1 | a0003 | c0004 | t0002 | g0180 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0320 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0208 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0317 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03225 | hp2 | a0005 | c0005 | t0001 | g0015 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03239 | hp1 | a0011 | c0009 | t0001 | g0049 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03239 | hp2 | a0012 | c0018 | t0001 | g0296 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0298 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03516 | hp1 | a0003 | c0004 | t0002 | g0183 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0212 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0312 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0326 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0311 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04184 | hp1 | a0014 | c0019 | t0001 | g0019 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0313 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0314 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18906 | hp2 | a0003 | c0004 | t0002 | g0184 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18973 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18984 | hp1 | a0015 | c0015 | t0001 | g0270 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19007 | hp2 | a0016 | c0007 | t0001 | g0047 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | LWK | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0324 | AFR | LWK | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20129 | hp1 | a0003 | c0004 | t0002 | g0181 | AFR | ASW | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0297 | AFR | ASW | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0281 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03471 | hp1 | a0013 | c0010 | t0001 | g0205 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0319 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
homoSapiens | chm13v2 | a0017 | c0011 | t0001 | g0187 | REF | REF | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0079 | REF | REF | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:128915125 | C | T | 1 | a0015 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.3274G>A | p.Val1092Ile | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/16 | 3403/3870 | 3274/3315 | 1092/1104 | chr3 | 128915125 | |||
chr3:128915468 | TTTC | T | 1 | a0004 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
disruptive_inframe_deletion | MODERATE | c.3009_3011delGAA | p.Lys1004del | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 14/16 | 3140/3870 | 3009/3315 | 1003/1104 | chr3 | 128915468 | |||
chr3:128916219 | G | A | 1 | a0006 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.2804C>T | p.Ala935Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2933/3870 | 2804/3315 | 935/1104 | chr3 | 128916219 | |||
chr3:128932735 | T | G | 3 | a0002 a0003 a0009 |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
missense_variant | MODERATE | c.2716A>C | p.Met906Leu | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2845/3870 | 2716/3315 | 906/1104 | chr3 | 128932735 | |||
chr3:128932737 | A | T | 1 | a0005 | 2 | HG01109.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.2714T>A | p.Leu905His | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2843/3870 | 2714/3315 | 905/1104 | chr3 | 128932737 | |||
chr3:128932953 | G | A | 1 | a0002 | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
missense_variant | MODERATE | c.2498C>T | p.Thr833Met | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2627/3870 | 2498/3315 | 833/1104 | chr3 | 128932953 | |||
chr3:128932957 | C | T | 1 | a0007 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.2494G>A | p.Val832Met | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2623/3870 | 2494/3315 | 832/1104 | chr3 | 128932957 | |||
chr3:128944223 | GCACCTGG others(2064): Show |
G | 1 | a0012 | 1 | HG03239.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1354-319_2258+847d others(2): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | chr3 | 128944223 | |||||||
chr3:128945073 | G | C | 1 | a0001 | 1 | HG01243.hp2 | missense_variant&splice_region_variant | MODERATE | c.2256C>G | p.Ser752Arg | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2385/3870 | 2256/3315 | 752/1104 | chr3 | 128945073 | |||
chr3:128945326 | T | G | 1 | a0001 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.2003A>C | p.Lys668Thr | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2132/3870 | 2003/3315 | 668/1104 | chr3 | 128945326 | |||
chr3:128945612 | G | A | 1 | a0001 | 2 | HG00423.hp2 HG02132.hp2 |
missense_variant | MODERATE | c.1717C>T | p.Leu573Phe | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1846/3870 | 1717/3315 | 573/1104 | chr3 | 128945612 | |||
chr3:128945782 | C | T | 1 | a0003 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1547G>A | p.Arg516His | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1676/3870 | 1547/3315 | 516/1104 | chr3 | 128945782 | |||
chr3:128945821 | T | C | 1 | a0002 | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
missense_variant | MODERATE | c.1508A>G | p.Glu503Gly | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1637/3870 | 1508/3315 | 503/1104 | chr3 | 128945821 | |||
chr3:128965578 | G | A | 1 | a0014 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1286C>T | p.Pro429Leu | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/16 | 1415/3870 | 1286/3315 | 429/1104 | chr3 | 128965578 | |||
chr3:128975786 | C | G | 1 | a0013 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1014G>C | p.Arg338Ser | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/16 | 1143/3870 | 1014/3315 | 338/1104 | chr3 | 128975786 | |||
chr3:128975880 | G | C | 1 | a0003 | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
missense_variant | MODERATE | c.920C>G | p.Thr307Ser | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/16 | 1049/3870 | 920/3315 | 307/1104 | chr3 | 128975880 | |||
chr3:128976994 | T | C | 1 | a0008 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.881A>G | p.Asp294Gly | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/16 | 1010/3870 | 881/3315 | 294/1104 | chr3 | 128976994 | |||
chr3:128993082 | A | G | 1 | a0011 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.223T>C | p.Cys75Arg | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 352/3870 | 223/3315 | 75/1104 | chr3 | 128993082 | |||
chr3:128993103 | C | T | 1 | a0010 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.202G>A | p.Asp68Asn | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 331/3870 | 202/3315 | 68/1104 | chr3 | 128993103 | |||
chr3:128993142 | T | C | 1 | a0004 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.163A>G | p.Ile55Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 292/3870 | 163/3315 | 55/1104 | chr3 | 128993142 | |||
chr3:128993185 | C | G | 1 | a0016 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.120G>C | p.Lys40Asn | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 249/3870 | 120/3315 | 40/1104 | chr3 | 128993185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:128915120 | T | G | 1 | a0001c0016 | 1 | HG02451.hp1 | splice_region_variant&synonymous_variant | LOW | c.3279A>C | p.Thr1093Thr | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/16 | 3408/3870 | 3279/3315 | 1093/1104 | chr3 | 128915120 | |||
chr3:128916212 | C | T | 1 | a0001c0014 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.2811G>A | p.Val937Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2940/3870 | 2811/3315 | 937/1104 | chr3 | 128916212 | |||
chr3:128916227 | C | T | 1 | a0004c0021 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.2796G>A | p.Lys932Lys | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2925/3870 | 2796/3315 | 932/1104 | chr3 | 128916227 | |||
chr3:128916230 | C | T | 1 | a0013c0010 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2793G>A | p.Pro931Pro | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2922/3870 | 2793/3315 | 931/1104 | chr3 | 128916230 | |||
chr3:128932736 | A | C | 3 | a0002c0002 a0003c0004 a0009c0013 |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
synonymous_variant | LOW | c.2715T>G | p.Leu905Leu | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2844/3870 | 2715/3315 | 905/1104 | chr3 | 128932736 | |||
chr3:128935160 | G | A | 1 | a0003c0004 | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
synonymous_variant | LOW | c.2418C>T | p.Asp806Asp | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/16 | 2547/3870 | 2418/3315 | 806/1104 | chr3 | 128935160 | |||
chr3:128945112 | G | A | 6 | a0001c0001 a0001c0003 a0004c0006 others(3): Show |
41 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(38): Show |
synonymous_variant | LOW | c.2217C>T | p.Ala739Ala | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2346/3870 | 2217/3315 | 739/1104 | chr3 | 128945112 | |||
chr3:128945148 | G | A | 4 | a0001c0001 a0006c0017 a0010c0008 others(1): Show |
49 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
synonymous_variant | LOW | c.2181C>T | p.Asp727Asp | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2310/3870 | 2181/3315 | 727/1104 | chr3 | 128945148 | |||
chr3:128945625 | G | A | 1 | a0001c0003 | 2 | HG02896.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.1704C>T | p.Val568Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1833/3870 | 1704/3315 | 568/1104 | chr3 | 128945625 | |||
chr3:128945676 | G | A | 1 | a0006c0017 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1653C>T | p.Asn551Asn | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1782/3870 | 1653/3315 | 551/1104 | chr3 | 128945676 | |||
chr3:128945706 | G | T | 4 | a0001c0001 a0006c0017 a0010c0008 others(1): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
synonymous_variant | LOW | c.1623C>A | p.Ala541Ala | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1752/3870 | 1623/3315 | 541/1104 | chr3 | 128945706 | |||
chr3:128945811 | G | T | 3 | a0001c0001 a0001c0003 a0005c0005 |
35 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(32): Show |
synonymous_variant | LOW | c.1518C>A | p.Pro506Pro | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1647/3870 | 1518/3315 | 506/1104 | chr3 | 128945811 | |||
chr3:128988764 | T | C | 1 | a0001c0003 | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
synonymous_variant | LOW | c.417A>G | p.Pro139Pro | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/16 | 546/3870 | 417/3315 | 139/1104 | chr3 | 128988764 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:128909880 | A | G | 1 | a0001c0001t0006 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*419T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 419 | chr3 | 128909880 | ||||||
chr3:128909966 | A | G | 3 | a0002c0002t0002 a0003c0004t0002 a0009c0013t0002 |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*333T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 333 | chr3 | 128909966 | ||||||
chr3:128910132 | C | A | 1 | a0001c0001t0007 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 167 | chr3 | 128910132 | ||||||
chr3:128910140 | C | T | 1 | a0001c0001t0005 | 2 | HG02280.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*159G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 159 | chr3 | 128910140 | ||||||
chr3:128910196 | CCTG | C | 1 | a0001c0001t0004 | 5 | HG00642.hp2 HG00733.hp2 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*102delCAG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 100 | chr3 | 128910196 | ||||||
chr3:128910273 | G | A | 1 | a0001c0001t0003 | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*26C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 26 | chr3 | 128910273 | ||||||
chr3:128910294 | G | C | 3 | a0002c0002t0002 a0003c0004t0002 a0009c0013t0002 |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 5 | chr3 | 128910294 | ||||||
chr3:128993991 | T | C | 1 | a0001c0001t0008 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/16 | 687 | chr3 | 128993991 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:128910434 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0295 |
3 | HG01081.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3281-101G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910434 | |||||||
chr3:128910489 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3281-156C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910489 | |||||||
chr3:128910575 | G | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3281-242C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910575 | |||||||
chr3:128910662 | C | CTGAT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(113): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.3281-333_3281-330d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910662 | |||||||
chr3:128910891 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.3281-558A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910891 | |||||||
chr3:128910918 | C | A | 1 | a0002c0002t0002g0326 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3281-585G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910918 | |||||||
chr3:128910939 | C | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3281-606G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910939 | |||||||
chr3:128911050 | T | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3281-717A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911050 | |||||||
chr3:128911118 | G | A | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3281-785C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911118 | |||||||
chr3:128911202 | G | A | 6 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0100 others(3): Show |
6 | HG00609.hp2 NA18965.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-869C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911202 | |||||||
chr3:128911206 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3281-873C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911206 | |||||||
chr3:128911214 | G | A | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.3281-881C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911214 | |||||||
chr3:128911217 | C | T | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-884G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911217 | |||||||
chr3:128911275 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3281-942G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911275 | |||||||
chr3:128911278 | C | G | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3281-945G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911278 | |||||||
chr3:128911342 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3281-1009C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911342 | |||||||
chr3:128911458 | T | C | 4 | a0002c0002t0002g0317 a0002c0002t0002g0318 a0002c0002t0002g0319 others(1): Show |
4 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1125A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911458 | |||||||
chr3:128911654 | C | G | 4 | a0001c0001t0001g0218 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1321G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911654 | |||||||
chr3:128911667 | CCT | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3281-1336_3281-133 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911667 | |||||||
chr3:128911736 | C | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3281-1403G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911736 | |||||||
chr3:128911736 | C | G | 7 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(4): Show |
7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3281-1403G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911736 | |||||||
chr3:128911792 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.3281-1459A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911792 | |||||||
chr3:128911966 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3281-1633G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911966 | |||||||
chr3:128911983 | G | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0331 |
2 | HG01261.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3281-1650C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911983 | |||||||
chr3:128912119 | T | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3281-1786A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912119 | |||||||
chr3:128912251 | C | A | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3281-1918G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912251 | |||||||
chr3:128912303 | G | C | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3281-1970C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912303 | |||||||
chr3:128912334 | C | T | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-2001G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912334 | |||||||
chr3:128912344 | C | T | 1 | a0001c0001t0004g0280 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3281-2011G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912344 | |||||||
chr3:128912448 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0086 |
2 | NA18999.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3281-2115G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912448 | |||||||
chr3:128912467 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3281-2134A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912467 | |||||||
chr3:128912598 | G | A | 1 | a0002c0002t0002g0302 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3281-2265C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912598 | |||||||
chr3:128912633 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0043 |
2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3281-2300G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912633 | |||||||
chr3:128912638 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3281-2305C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912638 | |||||||
chr3:128912675 | C | T | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-2342G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912675 | |||||||
chr3:128912829 | GGA | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+2288_3280+228 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912829 | |||||||
chr3:128912938 | T | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3280+2181A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912938 | |||||||
chr3:128913209 | C | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(23): Show |
27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3280+1910G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913209 | |||||||
chr3:128913210 | C | T | 1 | a0002c0002t0002g0302 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3280+1909G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913210 | |||||||
chr3:128913309 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3280+1810G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913309 | |||||||
chr3:128913477 | T | TTACACCA others(10): Show |
46 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(43): Show |
49 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.3280+1625_3280+164 others(21): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913477 | |||||||
chr3:128913561 | T | C | 1 | a0002c0002t0002g0326 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3280+1558A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913561 | |||||||
chr3:128913596 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3280+1523C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913596 | |||||||
chr3:128913611 | A | G | 33 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0037 others(30): Show |
34 | HG01167.hp1 HG01175.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.3280+1508T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913611 | |||||||
chr3:128913879 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0038 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3280+1240G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913879 | |||||||
chr3:128913926 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3280+1193C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913926 | |||||||
chr3:128913964 | C | T | 1 | a0004c0006t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3280+1155G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913964 | |||||||
chr3:128914027 | T | C | 4 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+1092A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914027 | |||||||
chr3:128914112 | C | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(24): Show |
28 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3280+1007G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914112 | |||||||
chr3:128914231 | A | G | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3280+888T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914231 | |||||||
chr3:128914296 | A | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG00423.hp2 HG00558.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.3280+823T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914296 | |||||||
chr3:128914537 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3280+582A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914537 | |||||||
chr3:128914627 | CAG | C | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0294 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3280+490_3280+491d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914627 | |||||||
chr3:128914664 | C | T | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3280+455G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914664 | |||||||
chr3:128914919 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3280+200C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914919 | |||||||
chr3:128914965 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
197 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.3280+154A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914965 | |||||||
chr3:128915319 | T | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3123+38A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 14/15 | chr3 | 128915319 | |||||||
chr3:128915730 | T | C | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2917-167A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915730 | |||||||
chr3:128915743 | G | A | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2917-180C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915743 | |||||||
chr3:128915804 | G | A | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2917-241C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915804 | |||||||
chr3:128915830 | A | G | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2917-267T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915830 | |||||||
chr3:128915930 | G | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2916+177C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915930 | |||||||
chr3:128916083 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0044 others(62): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.2916+24G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128916083 | |||||||
chr3:128916095 | T | C | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2916+12A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128916095 | |||||||
chr3:128916337 | G | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2752-66C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916337 | |||||||
chr3:128916555 | A | C | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2752-284T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916555 | |||||||
chr3:128916616 | CA | C | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-346delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916616 | |||||||
chr3:128916618 | A | G | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-347T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916618 | |||||||
chr3:128916619 | C | G | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-348G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916619 | |||||||
chr3:128916720 | G | A | 4 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0294 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-449C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916720 | |||||||
chr3:128916895 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2752-624C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916895 | |||||||
chr3:128917105 | A | G | 2 | a0004c0006t0001g0329 a0004c0021t0001g0328 |
2 | HG00642.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2752-834T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917105 | |||||||
chr3:128917156 | G | T | 1 | a0001c0001t0001g0114 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2752-885C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917156 | |||||||
chr3:128917262 | G | A | 6 | a0001c0001t0001g0082 a0001c0001t0001g0222 a0001c0001t0001g0225 others(3): Show |
6 | HG02040.hp2 HG02293.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.2752-991C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917262 | |||||||
chr3:128917444 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-1173C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917444 | |||||||
chr3:128917757 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2752-1486C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917757 | |||||||
chr3:128917791 | C | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2752-1520G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917791 | |||||||
chr3:128917872 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.2752-1601T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917872 | |||||||
chr3:128917934 | GAC | G | 7 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(4): Show |
7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2752-1665_2752-166 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917934 | |||||||
chr3:128918118 | A | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(110): Show |
115 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2752-1847T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918118 | |||||||
chr3:128918182 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
164 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.2752-1911A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918182 | |||||||
chr3:128918212 | G | A | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2752-1941C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918212 | |||||||
chr3:128918262 | A | T | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2752-1991T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918262 | |||||||
chr3:128918467 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2752-2196G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918467 | |||||||
chr3:128918489 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2752-2218T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918489 | |||||||
chr3:128918564 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2752-2293G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918564 | |||||||
chr3:128918793 | T | C | 2 | a0001c0001t0001g0164 a0016c0007t0001g0047 |
2 | NA19007.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2752-2522A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918793 | |||||||
chr3:128918851 | C | T | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2752-2580G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918851 | |||||||
chr3:128918940 | A | AT | 14 | a0001c0001t0001g0031 a0001c0001t0001g0068 a0001c0001t0001g0070 others(11): Show |
14 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.2752-2670dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | |||||||
chr3:128918940 | AT | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(106): Show |
111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.2752-2670delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | |||||||
chr3:128918940 | ATT | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0219 a0001c0001t0001g0252 others(8): Show |
11 | HG00642.hp1 HG01071.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2752-2671_2752-267 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | |||||||
chr3:128918940 | ATTT | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(31): Show |
35 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2752-2672_2752-267 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | |||||||
chr3:128918940 | ATTTTTTT | A | 21 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(18): Show |
22 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.2752-2676_2752-267 others(11): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | |||||||
chr3:128918972 | A | C | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2752-2701T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918972 | |||||||
chr3:128918972 | A | T | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2752-2701T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918972 | |||||||
chr3:128919009 | G | A | 8 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(5): Show |
8 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2752-2738C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919009 | |||||||
chr3:128919040 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2752-2769G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919040 | |||||||
chr3:128919221 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2752-2950C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919221 | |||||||
chr3:128919224 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2752-2953C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919224 | |||||||
chr3:128919247 | A | AT | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-2977dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919247 | |||||||
chr3:128919748 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2752-3477G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919748 | |||||||
chr3:128919783 | A | G | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-3512T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919783 | |||||||
chr3:128919926 | C | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
12 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2752-3655G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919926 | |||||||
chr3:128919958 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2752-3687G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919958 | |||||||
chr3:128919987 | C | G | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-3716G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919987 | |||||||
chr3:128920116 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2752-3845T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920116 | |||||||
chr3:128920229 | C | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-3958G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920229 | |||||||
chr3:128920262 | G | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2752-3991C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920262 | |||||||
chr3:128920488 | A | G | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-4217T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920488 | |||||||
chr3:128920768 | C | T | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-4497G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920768 | |||||||
chr3:128920901 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2752-4630G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920901 | |||||||
chr3:128920984 | T | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-4713A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920984 | |||||||
chr3:128921005 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2752-4734T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921005 | |||||||
chr3:128921068 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-4797C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921068 | |||||||
chr3:128921209 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2752-4938T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921209 | |||||||
chr3:128921264 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2752-4993G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921264 | |||||||
chr3:128921287 | C | T | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2752-5016G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921287 | |||||||
chr3:128921331 | C | A | 1 | a0004c0006t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2752-5060G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921331 | |||||||
chr3:128921396 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
161 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2752-5125G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921396 | |||||||
chr3:128921402 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0216 a0001c0001t0001g0252 |
3 | HG01496.hp2 HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.2752-5131T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921402 | |||||||
chr3:128921434 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(114): Show |
119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2752-5163T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921434 | |||||||
chr3:128921541 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2752-5270T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921541 | |||||||
chr3:128921751 | C | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2752-5480G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921751 | |||||||
chr3:128921770 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2752-5499G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921770 | |||||||
chr3:128922065 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2752-5794G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922065 | |||||||
chr3:128922136 | G | C | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2752-5865C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922136 | |||||||
chr3:128922144 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2752-5873A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922144 | |||||||
chr3:128922166 | C | T | 3 | a0002c0002t0002g0300 a0002c0002t0002g0301 a0002c0002t0002g0303 |
3 | HG02056.hp2 NA18985.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2752-5895G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922166 | |||||||
chr3:128922183 | C | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-5912G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922183 | |||||||
chr3:128922183 | CA | C | 31 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0002c0002t0002g0008 others(28): Show |
32 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.2752-5913delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922183 | |||||||
chr3:128922212 | G | A | 1 | a0015c0015t0001g0270 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2752-5941C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922212 | |||||||
chr3:128922342 | C | CA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0186 a0001c0001t0001g0331 others(3): Show |
6 | HG01069.hp1 HG01261.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2752-6072dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922342 | |||||||
chr3:128922342 | CA | C | 33 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
34 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(31): Show |
intron_variant | MODIFIER | c.2752-6072delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922342 | |||||||
chr3:128922357 | T | C | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-6086A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922357 | |||||||
chr3:128922437 | A | G | 17 | a0001c0001t0001g0130 a0001c0001t0001g0154 a0001c0001t0001g0158 others(14): Show |
17 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.2752-6166T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922437 | |||||||
chr3:128922499 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
12 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2752-6228C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922499 | |||||||
chr3:128922511 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-6240C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922511 | |||||||
chr3:128922621 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-6350T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922621 | |||||||
chr3:128922666 | C | T | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-6395G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922666 | |||||||
chr3:128923076 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2752-6805C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923076 | |||||||
chr3:128923108 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-6837C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923108 | |||||||
chr3:128923135 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2752-6864C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923135 | |||||||
chr3:128923152 | CAGG | C | 41 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(38): Show |
42 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.2752-6884_2752-688 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923152 | |||||||
chr3:128923205 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
203 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.2752-6934T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923205 | |||||||
chr3:128923233 | G | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-6962C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923233 | |||||||
chr3:128923303 | T | C | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2752-7032A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923303 | |||||||
chr3:128923619 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2752-7348G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923619 | |||||||
chr3:128923868 | T | C | 1 | a0001c0003t0001g0211 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2752-7597A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923868 | |||||||
chr3:128924038 | G | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-7767C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924038 | |||||||
chr3:128924093 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0076 others(19): Show |
24 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2752-7822G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924093 | |||||||
chr3:128924207 | G | C | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-7936C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924207 | |||||||
chr3:128924263 | G | C | 1 | a0001c0001t0007g0080 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2752-7992C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924263 | |||||||
chr3:128924301 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(114): Show |
119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2752-8030C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924301 | |||||||
chr3:128924312 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2752-8041G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924312 | |||||||
chr3:128924432 | C | CT | 22 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0074 others(19): Show |
22 | HG00280.hp2 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2752-8162dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924432 | C | CTT | 37 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
40 | HG00323.hp1 HG00423.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2752-8163_2752-816 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924432 | C | CTTT | 9 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 others(6): Show |
9 | HG00642.hp1 HG00735.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2752-8164_2752-816 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924432 | CT | C | 16 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(13): Show |
16 | HG00280.hp1 HG01169.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.2752-8162delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924432 | CTTTT | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0109 a0001c0001t0001g0125 others(3): Show |
6 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2752-8165_2752-816 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924432 | CTTTTT | C | 24 | a0001c0001t0001g0237 a0001c0001t0001g0251 a0001c0001t0001g0254 others(21): Show |
25 | HG01928.hp1 HG01981.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.2752-8166_2752-816 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924432 | CTTTTTT | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0021 others(62): Show |
66 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2752-8167_2752-816 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924432 | CTTTTTTT | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
49 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.2752-8168_2752-816 others(11): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | |||||||
chr3:128924466 | CAG | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-8197_2752-819 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924466 | |||||||
chr3:128924474 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(119): Show |
124 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.2752-8203G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924474 | |||||||
chr3:128924505 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+8195G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924505 | |||||||
chr3:128924531 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+8169T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924531 | |||||||
chr3:128924532 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+8168A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924532 | |||||||
chr3:128924618 | A | ATTT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
158 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.2751+8079_2751+808 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924618 | |||||||
chr3:128924710 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2751+7990C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924710 | |||||||
chr3:128924727 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2751+7973C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924727 | |||||||
chr3:128924893 | C | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(107): Show |
112 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2751+7807G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924893 | |||||||
chr3:128924900 | C | G | 1 | a0001c0001t0001g0219 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2751+7800G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924900 | |||||||
chr3:128924923 | G | GT | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+7776dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924923 | |||||||
chr3:128924969 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+7731G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924969 | |||||||
chr3:128924974 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0216 |
2 | HG01496.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2751+7726G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924974 | |||||||
chr3:128925064 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2751+7636A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925064 | |||||||
chr3:128925172 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+7528A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925172 | |||||||
chr3:128925204 | T | C | 1 | a0001c0001t0005g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2751+7496A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925204 | |||||||
chr3:128925524 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0038 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2751+7176G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925524 | |||||||
chr3:128925615 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
121 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.2751+7085T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925615 | |||||||
chr3:128925752 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(114): Show |
119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2751+6948T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925752 | |||||||
chr3:128925769 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+6931C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925769 | |||||||
chr3:128925973 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+6727G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925973 | |||||||
chr3:128925997 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+6703A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925997 | |||||||
chr3:128926077 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+6623C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926077 | |||||||
chr3:128926113 | G | A | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2751+6587C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926113 | |||||||
chr3:128926180 | G | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA19076.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2751+6520C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926180 | |||||||
chr3:128926196 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+6504C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926196 | |||||||
chr3:128926206 | C | G | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2751+6494G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926206 | |||||||
chr3:128926246 | CGCCTGTA | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+6447_2751+645 others(11): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926246 | |||||||
chr3:128926369 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2751+6331G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926369 | |||||||
chr3:128926478 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2751+6222C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926478 | |||||||
chr3:128926586 | G | C | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2751+6114C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926586 | |||||||
chr3:128926756 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+5944G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926756 | |||||||
chr3:128926867 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2751+5833C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926867 | |||||||
chr3:128926891 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+5809A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926891 | |||||||
chr3:128926944 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2751+5756T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926944 | |||||||
chr3:128926990 | A | G | 1 | a0002c0002t0002g0008 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2751+5710T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926990 | |||||||
chr3:128927066 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2751+5634G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927066 | |||||||
chr3:128927104 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+5596T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927104 | |||||||
chr3:128927125 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+5575G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927125 | |||||||
chr3:128927201 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2751+5499C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927201 | |||||||
chr3:128927282 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2751+5418A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927282 | |||||||
chr3:128927321 | A | AAAGG | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2751+5375_2751+537 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927321 | |||||||
chr3:128927446 | C | T | 1 | a0002c0002t0002g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2751+5254G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927446 | |||||||
chr3:128927449 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+5251C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927449 | |||||||
chr3:128927515 | A | G | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+5185T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927515 | |||||||
chr3:128927640 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+5060G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927640 | |||||||
chr3:128927723 | C | CA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
91 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2751+4976dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927723 | |||||||
chr3:128927723 | C | CAA | 17 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0005g0332 others(14): Show |
17 | HG00639.hp2 HG01257.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2751+4975_2751+497 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927723 | |||||||
chr3:128927723 | CA | C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0130 a0001c0001t0001g0154 others(6): Show |
9 | HG01167.hp2 HG01346.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2751+4976delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927723 | |||||||
chr3:128927748 | T | C | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+4952A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927748 | |||||||
chr3:128927904 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2751+4796A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927904 | |||||||
chr3:128928109 | C | T | 1 | a0001c0003t0001g0208 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2751+4591G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928109 | |||||||
chr3:128928122 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+4578C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928122 | |||||||
chr3:128928170 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0201 |
2 | HG00438.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2751+4530C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928170 | |||||||
chr3:128928208 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2751+4492C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928208 | |||||||
chr3:128928247 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+4453G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928247 | |||||||
chr3:128928270 | A | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2751+4430T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928270 | |||||||
chr3:128928298 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+4402A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928298 | |||||||
chr3:128928518 | G | C | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2751+4182C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928518 | |||||||
chr3:128928636 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2751+4064G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928636 | |||||||
chr3:128928779 | CAT | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(23): Show |
27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2751+3919_2751+392 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928779 | |||||||
chr3:128928979 | C | T | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2751+3721G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928979 | |||||||
chr3:128928980 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+3720T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928980 | |||||||
chr3:128929274 | T | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.2751+3426A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929274 | |||||||
chr3:128929349 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+3351C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929349 | |||||||
chr3:128929474 | A | G | 10 | a0001c0001t0001g0128 a0001c0001t0001g0277 a0001c0001t0001g0278 others(7): Show |
10 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.2751+3226T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929474 | |||||||
chr3:128929477 | G | A | 1 | a0002c0002t0002g0008 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2751+3223C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929477 | |||||||
chr3:128929581 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2751+3119A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929581 | |||||||
chr3:128929592 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2751+3108T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929592 | |||||||
chr3:128929603 | C | T | 32 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(29): Show |
33 | HG01255.hp2 HG02040.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.2751+3097G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929603 | |||||||
chr3:128929604 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2751+3096C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929604 | |||||||
chr3:128929759 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+2941C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929759 | |||||||
chr3:128929984 | T | C | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+2716A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929984 | |||||||
chr3:128930182 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+2518C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930182 | |||||||
chr3:128930238 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+2462G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930238 | |||||||
chr3:128930307 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2751+2393G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930307 | |||||||
chr3:128930486 | C | T | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+2214G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930486 | |||||||
chr3:128930522 | A | AGGTG | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+2174_2751+217 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930522 | |||||||
chr3:128930676 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2751+2024C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930676 | |||||||
chr3:128930696 | A | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0044 others(66): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.2751+2004T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930696 | |||||||
chr3:128930719 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+1981G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930719 | |||||||
chr3:128930743 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01167.hp1 HG01175.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2751+1957A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930743 | |||||||
chr3:128930803 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2751+1897A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930803 | |||||||
chr3:128930910 | G | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+1790C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930910 | |||||||
chr3:128931036 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2751+1664C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931036 | |||||||
chr3:128931059 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2751+1641G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931059 | |||||||
chr3:128931107 | G | C | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+1593C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931107 | |||||||
chr3:128931125 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+1575C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931125 | |||||||
chr3:128931200 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0251 a0001c0001t0001g0255 others(1): Show |
4 | HG01255.hp1 HG01433.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+1500C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931200 | |||||||
chr3:128931336 | C | T | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+1364G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931336 | |||||||
chr3:128931356 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2751+1344G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931356 | |||||||
chr3:128931412 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+1288G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931412 | |||||||
chr3:128931417 | C | T | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2751+1283G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931417 | |||||||
chr3:128931432 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+1268C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931432 | |||||||
chr3:128931441 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2751+1225_2751+125 others(38): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931441 | |||||||
chr3:128931453 | G | GTA | 40 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+1245_2751+124 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931453 | |||||||
chr3:128931455 | A | G | 23 | a0001c0016t0001g0198 a0002c0002t0002g0008 a0002c0002t0002g0099 others(20): Show |
24 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.2751+1245T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931455 | |||||||
chr3:128931472 | C | CATATATA others(3): Show |
157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.2751+1227_2751+122 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931472 | |||||||
chr3:128931472 | C | CATATATA others(13): Show |
29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+1227_2751+122 others(24): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931472 | |||||||
chr3:128931479 | A | G | 2 | a0001c0001t0004g0273 a0001c0001t0004g0274 |
2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2751+1221T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931479 | |||||||
chr3:128931509 | A | G | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+1191T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931509 | |||||||
chr3:128931513 | ATATG | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0152 a0001c0001t0001g0155 others(3): Show |
7 | HG00423.hp1 HG01081.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+1183_2751+118 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931513 | |||||||
chr3:128931519 | ATGTATG | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0076 others(34): Show |
39 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2751+1175_2751+118 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931519 | |||||||
chr3:128931523 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2751+1177T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931523 | |||||||
chr3:128931523 | ATG | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(23): Show |
27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2751+1175_2751+117 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931523 | |||||||
chr3:128931525 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2751+1175C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931525 | |||||||
chr3:128931527 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+1173C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931527 | |||||||
chr3:128931527 | G | GTA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0046 others(77): Show |
82 | HG00423.hp2 HG00558.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.2751+1171_2751+117 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931527 | |||||||
chr3:128931527 | GTA | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0137 a0001c0001t0001g0283 others(5): Show |
8 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2751+1171_2751+117 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931527 | |||||||
chr3:128931529 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0076 others(36): Show |
41 | HG00323.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+1171T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931529 | |||||||
chr3:128931531 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2751+1169T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931531 | |||||||
chr3:128931590 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2751+1110A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931590 | |||||||
chr3:128931857 | T | TA | 23 | a0001c0001t0001g0193 a0002c0002t0002g0008 a0002c0002t0002g0099 others(20): Show |
24 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.2751+842dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931857 | |||||||
chr3:128931868 | T | TA | 6 | a0001c0001t0001g0035 a0001c0001t0001g0106 a0001c0001t0001g0131 others(3): Show |
6 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2751+831dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931868 | |||||||
chr3:128932097 | T | C | 30 | a0001c0001t0003g0147 a0002c0002t0002g0008 a0002c0002t0002g0099 others(27): Show |
31 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.2751+603A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932097 | |||||||
chr3:128932156 | A | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+544T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932156 | |||||||
chr3:128932332 | T | C | 4 | a0002c0002t0002g0317 a0002c0002t0002g0318 a0002c0002t0002g0319 others(1): Show |
4 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2751+368A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932332 | |||||||
chr3:128932342 | A | T | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2751+358T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932342 | |||||||
chr3:128932352 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2751+348A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932352 | |||||||
chr3:128932352 | T | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.2751+348A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932352 | |||||||
chr3:128932378 | T | TAC | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
148 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.2751+320_2751+321d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACAC | 12 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(9): Show |
12 | HG00639.hp1 HG01069.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.2751+318_2751+321d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACACACA others(3): Show |
6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2751+312_2751+321d others(12): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACACACA others(13): Show |
2 | a0002c0002t0002g0099 a0002c0002t0002g0312 |
2 | HG02040.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2751+321_2751+322i others(22): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACACACA others(17): Show |
9 | a0002c0002t0002g0008 a0002c0002t0002g0298 a0002c0002t0002g0300 others(6): Show |
10 | HG02056.hp2 HG03491.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.2751+321_2751+322i others(26): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACACACA others(19): Show |
2 | a0002c0002t0002g0313 a0002c0002t0002g0314 |
2 | HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2751+321_2751+322i others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACACACA others(21): Show |
4 | a0002c0002t0002g0297 a0002c0002t0002g0315 a0002c0002t0002g0317 others(1): Show |
4 | HG02683.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2751+321_2751+322i others(30): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACACACA others(23): Show |
3 | a0002c0002t0002g0321 a0002c0002t0002g0323 a0002c0002t0002g0324 |
3 | HG02055.hp2 HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2751+321_2751+322i others(32): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932378 | T | TACACACA others(27): Show |
1 | a0002c0002t0002g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2751+321_2751+322i others(36): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | |||||||
chr3:128932396 | CAT | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+302_2751+303d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932396 | |||||||
chr3:128932397 | A | ACACACAC others(19): Show |
1 | a0002c0002t0002g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2751+302_2751+303i others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932397 | |||||||
chr3:128932398 | T | C | 20 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(17): Show |
21 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.2751+302A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932398 | |||||||
chr3:128932681 | G | C | 7 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(4): Show |
7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2751+19C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932681 | |||||||
chr3:128932693 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(106): Show |
111 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(108): Show |
splice_region_variant&intron_variant | LOW | c.2751+7C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932693 | |||||||
chr3:128933038 | T | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0186 a0001c0001t0001g0331 others(2): Show |
5 | HG01069.hp1 HG01109.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2454-41A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933038 | |||||||
chr3:128933071 | G | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2454-74C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933071 | |||||||
chr3:128933398 | A | G | 8 | a0001c0001t0001g0171 a0003c0004t0002g0180 a0003c0004t0002g0181 others(5): Show |
8 | HG01346.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2454-401T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933398 | |||||||
chr3:128933441 | C | T | 13 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(10): Show |
13 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.2454-444G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933441 | |||||||
chr3:128933562 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2454-565C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933562 | |||||||
chr3:128933579 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2454-582T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933579 | |||||||
chr3:128933710 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(34): Show |
38 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.2454-713G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933710 | |||||||
chr3:128933793 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2454-796G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933793 | |||||||
chr3:128933933 | C | CTAG | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2454-939_2454-937d others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933933 | |||||||
chr3:128933951 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0295 |
3 | HG01081.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2454-954C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933951 | |||||||
chr3:128934134 | GTTCT | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
161 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2453+987_2453+990d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934134 | |||||||
chr3:128934142 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
161 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2453+983A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934142 | |||||||
chr3:128934296 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2453+829A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934296 | |||||||
chr3:128934466 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2453+659C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934466 | |||||||
chr3:128934481 | A | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2453+644T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934481 | |||||||
chr3:128934786 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2453+339G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934786 | |||||||
chr3:128934961 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0193 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2453+164C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934961 | |||||||
chr3:128935011 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2453+114C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935011 | |||||||
chr3:128935072 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2453+53C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935072 | |||||||
chr3:128935107 | C | G | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2453+18G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935107 | |||||||
chr3:128935109 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2453+16T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935109 | |||||||
chr3:128935335 | G | A | 1 | a0015c0015t0001g0270 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2259-16C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935335 | |||||||
chr3:128935471 | G | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-152C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935471 | |||||||
chr3:128935572 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2259-253G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935572 | |||||||
chr3:128935684 | C | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-365G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935684 | |||||||
chr3:128935793 | C | T | 33 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
34 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(31): Show |
intron_variant | MODIFIER | c.2259-474G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935793 | |||||||
chr3:128936304 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-985C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936304 | |||||||
chr3:128936464 | T | C | 31 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0002c0002t0002g0008 others(28): Show |
32 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.2259-1145A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936464 | |||||||
chr3:128936498 | CAG | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-1181_2259-118 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936498 | |||||||
chr3:128936511 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-1192G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936511 | |||||||
chr3:128936513 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(23): Show |
27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2259-1194C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936513 | |||||||
chr3:128936657 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-1338G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936657 | |||||||
chr3:128936704 | A | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2259-1385T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936704 | |||||||
chr3:128936800 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2259-1481A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936800 | |||||||
chr3:128936922 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2259-1603G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936922 | |||||||
chr3:128936927 | C | A | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259-1608G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936927 | |||||||
chr3:128937053 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2259-1734G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937053 | |||||||
chr3:128937250 | CT | C | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-1932delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937250 | |||||||
chr3:128937258 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259-1939C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937258 | |||||||
chr3:128937303 | A | G | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2259-1984T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937303 | |||||||
chr3:128937312 | C | CA | 29 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0075 others(26): Show |
30 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.2259-1994dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937312 | |||||||
chr3:128937312 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2259-1994delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937312 | |||||||
chr3:128937332 | A | AAC | 9 | a0002c0002t0002g0303 a0002c0002t0002g0316 a0002c0002t0002g0317 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2259-2014_2259-201 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937332 | |||||||
chr3:128937332 | A | AC | 18 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(15): Show |
19 | HG02040.hp1 HG02056.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.2259-2014dupG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937332 | |||||||
chr3:128937332 | A | C | 1 | a0003c0004t0002g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2259-2013T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937332 | |||||||
chr3:128937341 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2259-2022T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937341 | |||||||
chr3:128937379 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
157 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.2259-2060C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937379 | |||||||
chr3:128937383 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
152 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.2259-2064A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937383 | |||||||
chr3:128937461 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2259-2142C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937461 | |||||||
chr3:128937513 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2259-2194A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937513 | |||||||
chr3:128937542 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2259-2223C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937542 | |||||||
chr3:128937604 | CA | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
191 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.2259-2286delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937604 | |||||||
chr3:128937838 | G | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-2519C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937838 | |||||||
chr3:128937861 | G | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-2542C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937861 | |||||||
chr3:128937938 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2259-2619G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937938 | |||||||
chr3:128938072 | G | GA | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2259-2754dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938072 | |||||||
chr3:128938160 | G | A | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2259-2841C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938160 | |||||||
chr3:128938161 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2259-2842C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938161 | |||||||
chr3:128938179 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0271 |
2 | HG02293.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2259-2860A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938179 | |||||||
chr3:128938186 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2259-2867G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938186 | |||||||
chr3:128938236 | AAAAG | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-2921_2259-291 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938236 | |||||||
chr3:128938263 | C | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0076 others(19): Show |
24 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2259-2944G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938263 | |||||||
chr3:128938269 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2259-2950T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938269 | |||||||
chr3:128938463 | C | T | 7 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(4): Show |
7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2259-3144G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938463 | |||||||
chr3:128938491 | CT | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.2259-3173delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938491 | |||||||
chr3:128938516 | T | C | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2259-3197A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938516 | |||||||
chr3:128938533 | T | G | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3214A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938533 | |||||||
chr3:128938629 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2259-3310C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938629 | |||||||
chr3:128938650 | C | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-3331G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938650 | |||||||
chr3:128938651 | G | A | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2259-3332C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938651 | |||||||
chr3:128938652 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-3333G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938652 | |||||||
chr3:128938709 | G | T | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3390C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938709 | |||||||
chr3:128938734 | C | T | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-3415G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938734 | |||||||
chr3:128939046 | T | C | 1 | a0002c0002t0002g0315 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2259-3727A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939046 | |||||||
chr3:128939134 | T | C | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3815A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939134 | |||||||
chr3:128939208 | G | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-3889C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939208 | |||||||
chr3:128939264 | G | A | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3945C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939264 | |||||||
chr3:128939287 | C | T | 24 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0002c0002t0002g0008 others(21): Show |
25 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.2259-3968G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939287 | |||||||
chr3:128939295 | C | T | 1 | a0001c0001t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2259-3976G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939295 | |||||||
chr3:128939354 | G | T | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-4035C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939354 | |||||||
chr3:128939363 | T | G | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259-4044A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939363 | |||||||
chr3:128939418 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-4099C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939418 | |||||||
chr3:128939420 | G | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-4101C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939420 | |||||||
chr3:128939541 | CCAT | C | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2259-4225_2259-422 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939541 | |||||||
chr3:128939543 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2259-4224T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939543 | |||||||
chr3:128939649 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(113): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2259-4330C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939649 | |||||||
chr3:128939789 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2259-4470C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939789 | |||||||
chr3:128939839 | A | G | 7 | a0002c0002t0002g0297 a0002c0002t0002g0316 a0002c0002t0002g0317 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259-4520T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939839 | |||||||
chr3:128939849 | C | T | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-4530G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939849 | |||||||
chr3:128939872 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(143): Show |
149 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2259-4553T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939872 | |||||||
chr3:128939892 | C | T | 1 | a0006c0017t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2259-4573G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939892 | |||||||
chr3:128940119 | A | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
244 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.2259-4800T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940119 | |||||||
chr3:128940217 | G | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2258+4854C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940217 | |||||||
chr3:128940401 | T | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(43): Show |
47 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2258+4670A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940401 | |||||||
chr3:128940737 | A | G | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2258+4334T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940737 | |||||||
chr3:128940905 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258+4166T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940905 | |||||||
chr3:128940911 | C | T | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+4160G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940911 | |||||||
chr3:128941068 | A | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2258+4003T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941068 | |||||||
chr3:128941209 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2258+3862C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941209 | |||||||
chr3:128941209 | G | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2258+3862C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941209 | |||||||
chr3:128941376 | TTA | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2258+3693_2258+369 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941376 | |||||||
chr3:128941550 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0086 |
2 | NA18999.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2258+3521G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941550 | |||||||
chr3:128941633 | C | T | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258+3438G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941633 | |||||||
chr3:128941714 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(114): Show |
119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2258+3357G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941714 | |||||||
chr3:128941719 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(114): Show |
119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2258+3352G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941719 | |||||||
chr3:128941939 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2258+3132A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941939 | |||||||
chr3:128942009 | A | G | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2258+3062T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942009 | |||||||
chr3:128942076 | G | A | 7 | a0002c0002t0002g0297 a0002c0002t0002g0316 a0002c0002t0002g0317 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+2995C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942076 | |||||||
chr3:128942094 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
177 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.2258+2977T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942094 | |||||||
chr3:128942139 | A | G | 29 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(26): Show |
30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2258+2932T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942139 | |||||||
chr3:128942143 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2258+2928T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942143 | |||||||
chr3:128942165 | A | G | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258+2906T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942165 | |||||||
chr3:128942176 | G | A | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2258+2895C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942176 | |||||||
chr3:128942256 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2258+2815C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942256 | |||||||
chr3:128942298 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2258+2773G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942298 | |||||||
chr3:128942356 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2258+2715C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942356 | |||||||
chr3:128942417 | G | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(39): Show |
43 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2258+2654C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942417 | |||||||
chr3:128942442 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258+2629G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942442 | |||||||
chr3:128942677 | A | G | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258+2394T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942677 | |||||||
chr3:128942679 | C | CT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(111): Show |
116 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2258+2391dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942679 | |||||||
chr3:128942838 | C | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2258+2233G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942838 | |||||||
chr3:128942916 | C | CT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(105): Show |
110 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2258+2154dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | |||||||
chr3:128942916 | C | CTT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0231 a0001c0001t0001g0233 others(8): Show |
11 | HG00140.hp1 HG01243.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2258+2153_2258+215 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | |||||||
chr3:128942916 | CT | C | 50 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0064 others(47): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.2258+2154delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | |||||||
chr3:128942916 | CTTT | C | 21 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(18): Show |
22 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.2258+2152_2258+215 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | |||||||
chr3:128943078 | GC | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0186 others(23): Show |
27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2258+1992delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943078 | |||||||
chr3:128943373 | C | CCT | 64 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(61): Show |
66 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.2258+1697_2258+169 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943373 | |||||||
chr3:128943537 | C | CT | 25 | a0001c0001t0001g0092 a0001c0001t0001g0171 a0001c0001t0001g0234 others(22): Show |
26 | HG01346.hp2 HG02040.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2258+1533dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943537 | |||||||
chr3:128943557 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2258+1514G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943557 | |||||||
chr3:128943598 | C | T | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2258+1473G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943598 | |||||||
chr3:128943699 | G | C | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2258+1372C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943699 | |||||||
chr3:128943748 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
189 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.2258+1323T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943748 | |||||||
chr3:128943914 | T | TC | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0076 others(35): Show |
40 | HG00423.hp1 HG00735.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.2258+1156dupG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943914 | |||||||
chr3:128943914 | T | TCC | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.2258+1155_2258+115 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943914 | |||||||
chr3:128943919 | C | CCCCG | 22 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0189 others(19): Show |
22 | HG00642.hp2 HG00733.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.2258+1151_2258+115 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943919 | |||||||
chr3:128943919 | C | CCCCGT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0191 others(10): Show |
14 | HG00639.hp1 HG00639.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258+1151_2258+115 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943919 | |||||||
chr3:128943920 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2258+1151C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943920 | |||||||
chr3:128943920 | G | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0035 others(46): Show |
50 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.2258+1151C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943920 | |||||||
chr3:128943921 | T | C | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0076 others(43): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2258+1150A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943921 | |||||||
chr3:128943921 | T | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(128): Show |
135 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2258+1150A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943921 | |||||||
chr3:128943922 | T | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG00323.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+1149A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943922 | |||||||
chr3:128943922 | T | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0076 others(36): Show |
41 | HG00423.hp1 HG00735.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.2258+1149A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943922 | |||||||
chr3:128943923 | T | G | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG00323.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+1148A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943923 | |||||||
chr3:128943931 | T | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
117 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2258+1140A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943931 | |||||||
chr3:128943932 | T | G | 1 | a0001c0001t0001g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2258+1139A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943932 | |||||||
chr3:128944097 | T | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0076 others(39): Show |
44 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.2258+974A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944097 | |||||||
chr3:128944180 | AC | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2258+890delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944180 | |||||||
chr3:128944316 | T | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2258+755A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944316 | |||||||
chr3:128944721 | A | G | 7 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(4): Show |
7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258+350T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944721 | |||||||
chr3:128944758 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2258+313C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944758 | |||||||
chr3:128944875 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2258+196C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944875 | |||||||
chr3:128945018 | C | A | 1 | a0006c0017t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2258+53G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128945018 | |||||||
chr3:128945979 | C | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.1354-4G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128945979 | |||||||
chr3:128946042 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-67C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946042 | |||||||
chr3:128946064 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1354-89G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946064 | |||||||
chr3:128946170 | G | A | 4 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 others(1): Show |
4 | HG00642.hp1 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-195C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946170 | |||||||
chr3:128946176 | G | A | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-201C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946176 | |||||||
chr3:128946177 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1354-202C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946177 | |||||||
chr3:128946237 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-262T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946237 | |||||||
chr3:128946261 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1354-286T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946261 | |||||||
chr3:128946326 | AG | A | 10 | a0001c0001t0001g0035 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG00639.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1354-352delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946326 | |||||||
chr3:128946446 | C | A | 4 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 others(1): Show |
4 | HG00642.hp1 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-471G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946446 | |||||||
chr3:128946642 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1354-667C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946642 | |||||||
chr3:128946665 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1354-690G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946665 | |||||||
chr3:128946838 | C | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG00423.hp1 NA18960.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354-863G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946838 | |||||||
chr3:128946841 | G | C | 22 | a0002c0002t0002g0008 a0002c0002t0002g0099 a0002c0002t0002g0297 others(19): Show |
23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-866C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946841 | |||||||
chr3:128946947 | T | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0128 others(76): Show |
81 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1354-972A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946947 | |||||||
chr3:128947077 | A | T | 4 | a0001c0001t0001g0299 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-1102T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947077 | |||||||
chr3:128947186 | T | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
253 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1354-1211A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947186 | |||||||
chr3:128947230 | G | GA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0141 others(3): Show |
6 | HG00673.hp1 HG01243.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1354-1256dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947230 | |||||||
chr3:128947230 | G | GAA | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1257_1354-125 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947230 | |||||||
chr3:128947286 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1354-1311C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947286 | |||||||
chr3:128947340 | A | G | 1 | a0004c0006t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1354-1365T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947340 | |||||||
chr3:128947342 | A | T | 1 | a0004c0006t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1354-1367T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947342 | |||||||
chr3:128947350 | C | T | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1354-1375G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947350 | |||||||
chr3:128947588 | C | T | 1 | a0001c0014t0001g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1354-1613G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947588 | |||||||
chr3:128947643 | C | T | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-1668G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947643 | |||||||
chr3:128947678 | A | C | 3 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0013c0010t0001g0205 |
3 | HG02280.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1354-1703T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947678 | |||||||
chr3:128947693 | G | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(11): Show |
14 | HG00642.hp1 HG01255.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1354-1718C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947693 | |||||||
chr3:128947842 | GA | G | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1868delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947842 | |||||||
chr3:128948037 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-2062G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948037 | |||||||
chr3:128948298 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1354-2323C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948298 | |||||||
chr3:128948377 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1354-2403dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | |||||||
chr3:128948377 | C | CTT | 17 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0046 others(14): Show |
17 | HG00423.hp2 HG00438.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1354-2404_1354-240 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | |||||||
chr3:128948377 | CT | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0050 others(94): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1354-2403delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | |||||||
chr3:128948377 | CTTTTTTT others(4): Show |
C | 8 | a0001c0001t0001g0199 a0001c0001t0001g0230 a0001c0001t0001g0231 others(5): Show |
8 | HG02056.hp2 HG02976.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1354-2413_1354-240 others(15): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | |||||||
chr3:128948377 | CTTTTTTT others(5): Show |
C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(58): Show |
64 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.1354-2414_1354-240 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | |||||||
chr3:128948377 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-2421_1354-240 others(23): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | |||||||
chr3:128948406 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1354-2431A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948406 | |||||||
chr3:128948411 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-2436T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948411 | |||||||
chr3:128948513 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1354-2538G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948513 | |||||||
chr3:128948528 | A | AT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0152 others(9): Show |
13 | HG00423.hp1 HG01081.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-2554dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948528 | |||||||
chr3:128948528 | AT | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0188 others(26): Show |
30 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-2554delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948528 | |||||||
chr3:128948711 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0129 |
2 | NA18970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1354-2736C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948711 | |||||||
chr3:128948759 | A | G | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-2784T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948759 | |||||||
chr3:128948769 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1354-2794T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948769 | |||||||
chr3:128948820 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1354-2845C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948820 | |||||||
chr3:128948875 | G | A | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-2900C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948875 | |||||||
chr3:128948904 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1354-2929T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948904 | |||||||
chr3:128948926 | A | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG01175.hp2 HG01256.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1354-2951T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948926 | |||||||
chr3:128948934 | G | A | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-2959C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948934 | |||||||
chr3:128948981 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1354-3006C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948981 | |||||||
chr3:128949010 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-3035T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949010 | |||||||
chr3:128949133 | C | T | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1354-3158G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949133 | |||||||
chr3:128949164 | G | C | 23 | a0001c0001t0001g0053 a0001c0001t0001g0061 a0001c0001t0001g0091 others(20): Show |
23 | HG00323.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-3189C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949164 | |||||||
chr3:128949348 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1354-3373G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949348 | |||||||
chr3:128949375 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(12): Show |
16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1354-3400A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949375 | |||||||
chr3:128949403 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG00639.hp1 HG01516.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1354-3428C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949403 | |||||||
chr3:128949747 | C | T | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-3772G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949747 | |||||||
chr3:128949833 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-3858G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949833 | |||||||
chr3:128949836 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-3861C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949836 | |||||||
chr3:128949936 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(12): Show |
16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1354-3961G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949936 | |||||||
chr3:128950021 | T | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-4046A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950021 | |||||||
chr3:128950068 | T | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-4093A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950068 | |||||||
chr3:128950068 | T | TA | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-4094dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950068 | |||||||
chr3:128950344 | C | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-4369G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950344 | |||||||
chr3:128950421 | C | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-4446G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950421 | |||||||
chr3:128950464 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1354-4489T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950464 | |||||||
chr3:128950640 | G | C | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-4665C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950640 | |||||||
chr3:128950691 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
83 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1354-4716A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950691 | |||||||
chr3:128950809 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0125 others(26): Show |
30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-4834G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950809 | |||||||
chr3:128950911 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1354-4936C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950911 | |||||||
chr3:128951007 | C | A | 1 | a0014c0019t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1354-5032G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951007 | |||||||
chr3:128951020 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-5045G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951020 | |||||||
chr3:128951125 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
83 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1354-5150A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951125 | |||||||
chr3:128951236 | GA | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0299 others(42): Show |
47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1354-5262delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951236 | |||||||
chr3:128951324 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-5349C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951324 | |||||||
chr3:128951466 | G | A | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(9): Show |
12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-5491C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951466 | |||||||
chr3:128951603 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-5628T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951603 | |||||||
chr3:128951662 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-5687T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951662 | |||||||
chr3:128951734 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0103 |
2 | NA19002.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1354-5759T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951734 | |||||||
chr3:128951747 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1354-5772G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951747 | |||||||
chr3:128951766 | A | G | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(9): Show |
12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-5791T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951766 | |||||||
chr3:128951878 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1354-5903C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951878 | |||||||
chr3:128952121 | TTTC | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-6149_1354-614 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952121 | |||||||
chr3:128952136 | C | CT | 38 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0109 others(35): Show |
39 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1354-6162dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952136 | |||||||
chr3:128952136 | C | CTT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-6163_1354-616 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952136 | |||||||
chr3:128952136 | CT | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0083 a0001c0001t0001g0129 others(6): Show |
9 | HG01070.hp1 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1354-6162delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952136 | |||||||
chr3:128952168 | T | A | 1 | a0001c0001t0007g0080 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1354-6193A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952168 | |||||||
chr3:128952175 | G | A | 2 | a0001c0001t0003g0214 a0013c0010t0001g0205 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1354-6200C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952175 | |||||||
chr3:128952180 | G | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0125 others(26): Show |
30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-6205C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952180 | |||||||
chr3:128952298 | T | TA | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-6324dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952298 | |||||||
chr3:128952303 | T | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-6328A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952303 | |||||||
chr3:128952527 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1354-6552A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952527 | |||||||
chr3:128952572 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1354-6597T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952572 | |||||||
chr3:128952674 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1354-6699C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952674 | |||||||
chr3:128952738 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-6763C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952738 | |||||||
chr3:128952747 | C | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-6772G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952747 | |||||||
chr3:128952808 | G | A | 1 | a0011c0009t0001g0049 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1354-6833C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952808 | |||||||
chr3:128952814 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-6839C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952814 | |||||||
chr3:128952815 | G | A | 1 | a0002c0002t0002g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1354-6840C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952815 | |||||||
chr3:128953079 | A | C | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1354-7104T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953079 | |||||||
chr3:128953082 | A | C | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-7107T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953082 | |||||||
chr3:128953184 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1354-7209C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953184 | |||||||
chr3:128953303 | CAGG | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-7331_1354-732 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953303 | |||||||
chr3:128953331 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-7356G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953331 | |||||||
chr3:128953332 | G | A | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(9): Show |
12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-7357C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953332 | |||||||
chr3:128953387 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1354-7412G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953387 | |||||||
chr3:128953420 | G | C | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-7445C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953420 | |||||||
chr3:128953470 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(227): Show |
237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1354-7495T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953470 | |||||||
chr3:128953496 | C | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-7521G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953496 | |||||||
chr3:128953524 | AAAAG | A | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7553_1354-755 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953524 | |||||||
chr3:128953526 | AAGAAAGA others(2701): Show |
A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+9277_1354-755 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953526 | |||||||
chr3:128953567 | G | GTCTCCC | 15 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(12): Show |
15 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1354-7598_1354-759 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953567 | |||||||
chr3:128953567 | G | GTCTCCCT others(5): Show |
1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-7604_1354-759 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953567 | |||||||
chr3:128953576 | TCCCTCTC others(17): Show |
T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-7625_1354-760 others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953576 | |||||||
chr3:128953594 | T | C | 17 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(14): Show |
17 | HG00639.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1354-7619A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953594 | |||||||
chr3:128953594 | T | TCCCTCTC others(5): Show |
1 | a0001c0001t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-7620_1354-761 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953594 | |||||||
chr3:128953600 | C | T | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(7): Show |
10 | HG01255.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1354-7625G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953600 | |||||||
chr3:128953600 | CCCCTCTC others(5): Show |
C | 1 | a0001c0001t0001g0096 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1354-7637_1354-762 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953600 | |||||||
chr3:128953600 | CCCCTCTC others(11): Show |
C | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-7643_1354-762 others(22): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953600 | |||||||
chr3:128953604 | TCTCCCTC others(9): Show |
T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1354-7645_1354-763 others(20): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953604 | |||||||
chr3:128953606 | T | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(20): Show |
23 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-7631A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953606 | |||||||
chr3:128953609 | C | G | 2 | a0001c0003t0001g0210 a0001c0003t0001g0213 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1354-7634G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953609 | |||||||
chr3:128953609 | CTCTCCCT others(15): Show |
C | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1354-7656_1354-763 others(26): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953609 | |||||||
chr3:128953610 | TCTCCCTC others(3): Show |
T | 2 | a0001c0003t0001g0210 a0001c0003t0001g0213 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1354-7645_1354-763 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953610 | |||||||
chr3:128953612 | T | C | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-7637A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953612 | |||||||
chr3:128953615 | C | CTCCCTCT others(3): Show |
6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7641_1354-764 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953615 | |||||||
chr3:128953615 | C | G | 1 | a0005c0005t0001g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1354-7640G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953615 | |||||||
chr3:128953615 | CTCTCCCT others(9): Show |
C | 1 | a0001c0001t0001g0295 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1354-7656_1354-764 others(20): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953615 | |||||||
chr3:128953618 | T | C | 4 | a0001c0001t0003g0214 a0004c0006t0001g0329 a0004c0006t0001g0330 others(1): Show |
4 | HG00642.hp1 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354-7643A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953618 | |||||||
chr3:128953620 | C | CGT | 13 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(10): Show |
13 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-7646_1354-764 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953620 | |||||||
chr3:128953620 | C | T | 6 | a0001c0001t0003g0214 a0001c0001t0005g0332 a0001c0001t0005g0333 others(3): Show |
6 | HG00642.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7645G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953620 | |||||||
chr3:128953624 | CCTCTCCG others(9): Show |
C | 1 | a0001c0001t0001g0244 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1354-7665_1354-765 others(20): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953624 | |||||||
chr3:128953625 | C | CCCTCTCC others(17): Show |
6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7651_1354-765 others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953625 | |||||||
chr3:128953625 | C | CTCTCCG | 6 | a0001c0001t0001g0125 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7656_1354-765 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953625 | |||||||
chr3:128953625 | C | G | 24 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(21): Show |
24 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1354-7650G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953625 | |||||||
chr3:128953631 | G | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1354-7656C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953631 | |||||||
chr3:128953740 | C | A | 18 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(15): Show |
18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1354-7765G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953740 | |||||||
chr3:128953743 | GTGCCTGC others(4): Show |
G | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7779_1354-776 others(15): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953743 | |||||||
chr3:128953768 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1354-7793T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953768 | |||||||
chr3:128953790 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1354-7815C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953790 | |||||||
chr3:128953798 | G | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354-7823C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953798 | |||||||
chr3:128953816 | G | A | 6 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | HG00639.hp1 HG01516.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1354-7841C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953816 | |||||||
chr3:128953818 | GC | G | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7844delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953818 | |||||||
chr3:128953840 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1354-7865G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953840 | |||||||
chr3:128953854 | C | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0141 others(44): Show |
48 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1354-7879G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953854 | |||||||
chr3:128953920 | A | G | 2 | a0001c0001t0001g0130 a0009c0013t0002g0143 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1354-7945T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953920 | |||||||
chr3:128953974 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1354-7999C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953974 | |||||||
chr3:128954025 | A | AC | 10 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0075 others(7): Show |
10 | HG01123.hp1 HG01496.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1354-8051dupG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954025 | |||||||
chr3:128954061 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(12): Show |
16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1354-8086G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954061 | |||||||
chr3:128954097 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1354-8122C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954097 | |||||||
chr3:128954123 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1354-8148G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954123 | |||||||
chr3:128954137 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-8162G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954137 | |||||||
chr3:128954164 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-8189C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954164 | |||||||
chr3:128954178 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-8203C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954178 | |||||||
chr3:128954242 | C | T | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-8267G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954242 | |||||||
chr3:128954289 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-8314G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954289 | |||||||
chr3:128954319 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1354-8344G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954319 | |||||||
chr3:128954486 | C | G | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-8511G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954486 | |||||||
chr3:128954486 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-8511G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954486 | |||||||
chr3:128954498 | T | A | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-8523A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954498 | |||||||
chr3:128954498 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1354-8523A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954498 | |||||||
chr3:128954502 | C | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1354-8527G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954502 | |||||||
chr3:128954527 | C | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-8552G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954527 | |||||||
chr3:128954527 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-8552G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954527 | |||||||
chr3:128954537 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0125 others(26): Show |
30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-8562C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954537 | |||||||
chr3:128954544 | C | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-8569G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954544 | |||||||
chr3:128954565 | G | C | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(9): Show |
12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-8590C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954565 | |||||||
chr3:128954592 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0188 others(32): Show |
36 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1354-8617G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954592 | |||||||
chr3:128954602 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-8627C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954602 | |||||||
chr3:128954630 | G | A | 26 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0063 others(23): Show |
26 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1354-8655C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954630 | |||||||
chr3:128954635 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1354-8660C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954635 | |||||||
chr3:128954668 | T | C | 18 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(15): Show |
18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1354-8693A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954668 | |||||||
chr3:128954720 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1354-8745C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954720 | |||||||
chr3:128954739 | T | TGGGGGTG others(43): Show |
12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8765_1354-876 others(54): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954739 | |||||||
chr3:128954744 | G | C | 2 | a0001c0001t0001g0202 a0008c0020t0001g0110 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-8769C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954744 | |||||||
chr3:128954745 | G | A | 2 | a0001c0001t0001g0202 a0008c0020t0001g0110 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-8770C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954745 | |||||||
chr3:128954749 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8774T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954749 | |||||||
chr3:128954751 | CCCTCCGC others(168): Show |
C | 1 | a0001c0001t0001g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1354-8951_1354-877 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954751 | |||||||
chr3:128954754 | T | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0188 others(24): Show |
29 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1354-8779A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954754 | |||||||
chr3:128954756 | C | CT | 12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8782_1354-878 others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954756 | |||||||
chr3:128954770 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1354-8795G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954770 | |||||||
chr3:128954777 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0188 others(22): Show |
27 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1354-8802A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954777 | |||||||
chr3:128954779 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-8804C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954779 | |||||||
chr3:128954783 | GT | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8809delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954783 | |||||||
chr3:128954788 | G | GTGGGGGT others(54): Show |
1 | a0001c0001t0001g0194 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1354-8814_1354-881 others(65): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954788 | |||||||
chr3:128954788 | G | GTGGGGGT others(53): Show |
12 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1354-8814_1354-881 others(64): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954788 | |||||||
chr3:128954789 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8814C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954789 | |||||||
chr3:128954792 | G | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8817C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954792 | |||||||
chr3:128954795 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8820A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954795 | |||||||
chr3:128954802 | G | GGCCA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8828_1354-882 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954802 | |||||||
chr3:128954806 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8831C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954806 | |||||||
chr3:128954811 | T | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8836A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954811 | |||||||
chr3:128954812 | A | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8837T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954812 | |||||||
chr3:128954814 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8839A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954814 | |||||||
chr3:128954819 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8844T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954819 | |||||||
chr3:128954821 | A | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8846T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954821 | |||||||
chr3:128954826 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8851T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954826 | |||||||
chr3:128954829 | C | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8854G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954829 | |||||||
chr3:128954834 | TGCCCGGC others(42): Show |
T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0217 a0001c0001t0001g0227 others(9): Show |
13 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1354-8908_1354-886 others(53): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954834 | |||||||
chr3:128954838 | C | A | 1 | a0001c0003t0001g0208 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1354-8863G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954838 | |||||||
chr3:128954839 | G | A | 57 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0046 others(54): Show |
57 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1354-8864C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954839 | |||||||
chr3:128954840 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(17): Show |
20 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1354-8865C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954840 | |||||||
chr3:128954844 | G | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8869C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954844 | |||||||
chr3:128954846 | C | T | 2 | a0001c0001t0001g0202 a0008c0020t0001g0110 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-8871G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954846 | |||||||
chr3:128954848 | CCCCGTCC others(41): Show |
C | 1 | a0001c0001t0001g0234 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1354-8921_1354-887 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954848 | |||||||
chr3:128954851 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(40): Show |
44 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1354-8876G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954851 | |||||||
chr3:128954852 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1354-8877C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954852 | |||||||
chr3:128954857 | G | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8882C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954857 | |||||||
chr3:128954872 | G | T | 63 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0046 others(60): Show |
63 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8897C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954872 | |||||||
chr3:128954876 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8901C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954876 | |||||||
chr3:128954878 | CCCCCCGC others(41): Show |
C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0223 a0001c0001t0001g0231 others(1): Show |
4 | HG01496.hp2 HG02074.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-8951_1354-890 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954878 | |||||||
chr3:128954888 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0217 a0001c0001t0001g0227 others(8): Show |
12 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-8913C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954888 | |||||||
chr3:128954904 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
5 | HG02080.hp1 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1354-8929G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954904 | |||||||
chr3:128954915 | T | TG | 11 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0277 others(8): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-8941dupC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954915 | |||||||
chr3:128954915 | TGGGGGTG others(450): Show |
T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(30): Show |
34 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1354-9397_1354-894 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954915 | |||||||
chr3:128954916 | GGGGGTGT others(41): Show |
G | 64 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0130 others(61): Show |
64 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1354-8989_1354-894 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954916 | |||||||
chr3:128954916 | GGGGGTGT others(269): Show |
G | 2 | a0001c0001t0001g0202 a0008c0020t0001g0110 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-9217_1354-894 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954916 | |||||||
chr3:128954917 | GGGGTGTC others(40): Show |
G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0286 |
2 | HG02895.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1354-8989_1354-894 others(51): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954917 | |||||||
chr3:128954921 | T | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0188 others(22): Show |
27 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1354-8946A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954921 | |||||||
chr3:128954923 | T | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8948A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954923 | |||||||
chr3:128954924 | C | CCA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8950_1354-894 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954924 | |||||||
chr3:128954925 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8950C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954925 | |||||||
chr3:128954926 | G | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8951C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954926 | |||||||
chr3:128954932 | C | CT | 12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8958_1354-895 others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954932 | |||||||
chr3:128954932 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0108 a0001c0001t0001g0188 others(11): Show |
15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1354-8957G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954932 | |||||||
chr3:128954935 | C | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8960G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954935 | |||||||
chr3:128954964 | T | TG | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
84 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1354-8990dupC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954964 | |||||||
chr3:128954969 | C | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
170 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1354-8994G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954969 | |||||||
chr3:128954970 | G | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0055 others(65): Show |
69 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1354-8995C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954970 | |||||||
chr3:128954995 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1354-9020C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954995 | |||||||
chr3:128955032 | A | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0108 others(24): Show |
29 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1354-9057T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955032 | |||||||
chr3:128955033 | CCCCTACT others(30): Show |
C | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9095_1354-905 others(41): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955033 | |||||||
chr3:128955072 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0108 others(30): Show |
35 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-9097G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955072 | |||||||
chr3:128955077 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1354-9102G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955077 | |||||||
chr3:128955083 | C | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-9108G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955083 | |||||||
chr3:128955106 | C | T | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(9): Show |
12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9131G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955106 | |||||||
chr3:128955109 | C | T | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(9): Show |
12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9134G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955109 | |||||||
chr3:128955109 | CGCCCGGC others(44): Show |
C | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-9185_1354-913 others(55): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955109 | |||||||
chr3:128955114 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-9139C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955114 | |||||||
chr3:128955126 | CG | C | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-9152delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955126 | |||||||
chr3:128955142 | GGGGGGGG others(43): Show |
G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0108 a0001c0001t0001g0188 others(21): Show |
25 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1354-9217_1354-916 others(54): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955142 | |||||||
chr3:128955143 | GGGGGGGT others(42): Show |
G | 7 | a0001c0001t0001g0004 a0001c0001t0003g0144 a0001c0001t0003g0145 others(4): Show |
8 | HG00642.hp2 HG01123.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1354-9217_1354-916 others(53): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955143 | |||||||
chr3:128955144 | GGGGGGTC others(41): Show |
G | 1 | a0001c0001t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1354-9217_1354-917 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955144 | |||||||
chr3:128955150 | T | C | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9175A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955150 | |||||||
chr3:128955160 | T | TGCCCGGC others(120): Show |
12 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0003t0001g0150 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-9186_1354-918 others(131): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955160 | |||||||
chr3:128955163 | C | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9188G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955163 | |||||||
chr3:128955165 | G | A | 3 | a0001c0001t0001g0294 a0001c0001t0005g0332 a0001c0001t0005g0333 |
3 | HG02280.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9190C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955165 | |||||||
chr3:128955165 | G | GGCCAGCC others(120): Show |
2 | a0001c0001t0001g0038 a0015c0015t0001g0270 |
2 | HG02717.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1354-9191_1354-919 others(131): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955165 | |||||||
chr3:128955178 | G | GTCCGGGA others(120): Show |
1 | a0001c0003t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1354-9204_1354-920 others(131): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955178 | |||||||
chr3:128955192 | T | TG | 19 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0066 others(16): Show |
19 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1354-9218dupC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955192 | |||||||
chr3:128955192 | T | TGGGGGGG others(173): Show |
1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1354-9218_1354-921 others(184): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955192 | |||||||
chr3:128955194 | G | C | 1 | a0001c0001t0004g0281 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1354-9219C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955194 | |||||||
chr3:128955229 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1354-9254C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955229 | |||||||
chr3:128955246 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9271G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955246 | |||||||
chr3:128955275 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1354-9300C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955275 | |||||||
chr3:128955301 | T | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(54): Show |
59 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1354-9326A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955301 | |||||||
chr3:128955301 | T | TGCCCCAT others(173): Show |
1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1354-9327_1354-932 others(184): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955301 | |||||||
chr3:128955301 | T | TGCCCCGT others(172): Show |
6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-9327_1354-932 others(183): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955301 | |||||||
chr3:128955306 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0277 others(13): Show |
17 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1354-9331G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955306 | |||||||
chr3:128955311 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(2): Show |
5 | HG00642.hp1 HG01255.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-9336C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955311 | |||||||
chr3:128955312 | CGAGGGAG others(222): Show |
C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0125 others(25): Show |
29 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1354-9566_1354-933 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955312 | |||||||
chr3:128955322 | GGGGGGGT others(221): Show |
G | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1354-9575_1354-934 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955322 | |||||||
chr3:128955332 | GC | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
134 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1354-9358delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955332 | |||||||
chr3:128955333 | C | CCCCCCAC others(171): Show |
1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955333 | C | CCCCCCGC others(171): Show |
7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0283 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955333 | C | CCCCCCGC others(171): Show |
1 | a0001c0001t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955333 | C | CCCCCCGC others(173): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0186 |
2 | HG01175.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(184): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955333 | C | CCCCCCGC others(172): Show |
12 | a0001c0001t0001g0050 a0001c0001t0001g0059 a0001c0001t0001g0067 others(9): Show |
12 | HG01255.hp2 HG01934.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(183): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955333 | C | CCCCCCGC others(171): Show |
1 | a0001c0001t0001g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955333 | C | CCCCCCGC others(172): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0124 |
2 | HG01934.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(183): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955333 | C | CCCCCCGC others(171): Show |
79 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(76): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | |||||||
chr3:128955339 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01255.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-9364G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955339 | |||||||
chr3:128955340 | G | A | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-9365C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955340 | |||||||
chr3:128955344 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0046 others(63): Show |
67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9369C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955344 | |||||||
chr3:128955346 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-9371G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955346 | |||||||
chr3:128955371 | TG | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1354-9397delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955371 | |||||||
chr3:128955372 | G | GGGGGGGG others(171): Show |
1 | a0001c0001t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1354-9398_1354-939 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955372 | |||||||
chr3:128955409 | G | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA19076.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1354-9434C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955409 | |||||||
chr3:128955427 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-9452C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955427 | |||||||
chr3:128955473 | T | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0046 others(64): Show |
68 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1354-9498A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955473 | |||||||
chr3:128955482 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1354-9507C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955482 | |||||||
chr3:128955486 | C | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0046 others(63): Show |
67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9511G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955486 | |||||||
chr3:128955487 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0003g0214 a0001c0003t0001g0150 others(10): Show |
13 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-9512C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955487 | |||||||
chr3:128955492 | G | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0046 others(62): Show |
66 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1354-9517C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955492 | |||||||
chr3:128955492 | G | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0290 |
2 | HG02074.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1354-9517C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955492 | |||||||
chr3:128955501 | TG | T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(164): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1354-9527delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955501 | |||||||
chr3:128955501 | TGGGGGGG others(43): Show |
T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
36 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1354-9576_1354-952 others(54): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955501 | |||||||
chr3:128955502 | G | GGGGGGGT others(170): Show |
1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-9528_1354-952 others(181): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955502 | |||||||
chr3:128955519 | G | A | 1 | a0004c0006t0001g0329 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1354-9544C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955519 | |||||||
chr3:128955520 | A | C | 66 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0046 others(63): Show |
67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9545T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955520 | |||||||
chr3:128955530 | C | T | 2 | a0004c0006t0001g0329 a0004c0021t0001g0328 |
2 | HG00642.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1354-9555G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955530 | |||||||
chr3:128955531 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1354-9556C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955531 | |||||||
chr3:128955536 | A | G | 66 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0046 others(63): Show |
67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9561T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955536 | |||||||
chr3:128955539 | C | T | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(9): Show |
12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9564G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955539 | |||||||
chr3:128955540 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1354-9565C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955540 | |||||||
chr3:128955550 | TG | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0217 a0001c0001t0001g0237 others(7): Show |
11 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1354-9576delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955550 | |||||||
chr3:128955551 | G | GGGGGGGG others(121): Show |
1 | a0001c0001t0001g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1354-9577_1354-957 others(132): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | |||||||
chr3:128955551 | G | GGGGGGGG others(121): Show |
53 | a0001c0001t0001g0046 a0001c0001t0001g0216 a0001c0001t0001g0218 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1354-9577_1354-957 others(132): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | |||||||
chr3:128955551 | G | GGGGGGGT others(171): Show |
1 | a0001c0001t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1354-9577_1354-957 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | |||||||
chr3:128955551 | G | T | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-9576C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | |||||||
chr3:128955572 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-9597C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955572 | |||||||
chr3:128955580 | G | A | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1354-9605C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955580 | |||||||
chr3:128955586 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1354-9611G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955586 | |||||||
chr3:128955589 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1354-9614T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955589 | |||||||
chr3:128955612 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1354-9637G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955612 | |||||||
chr3:128955650 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1354-9675T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955650 | |||||||
chr3:128955673 | G | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-9698C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955673 | |||||||
chr3:128955696 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1354-9721C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955696 | |||||||
chr3:128955727 | T | C | 1 | a0001c0001t0006g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1354-9752A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955727 | |||||||
chr3:128955735 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1354-9760G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955735 | |||||||
chr3:128955913 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0175 |
3 | HG02109.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1353+9598G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955913 | |||||||
chr3:128955979 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1353+9532A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955979 | |||||||
chr3:128955990 | A | C | 1 | a0001c0001t0006g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1353+9521T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955990 | |||||||
chr3:128956080 | T | C | 9 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(6): Show |
9 | HG01255.hp1 HG01433.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1353+9431A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956080 | |||||||
chr3:128956184 | T | A | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1353+9327A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956184 | |||||||
chr3:128956184 | TA | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0070 others(12): Show |
16 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9326delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956184 | |||||||
chr3:128956192 | A | T | 16 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(13): Show |
16 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9319T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956192 | |||||||
chr3:128956193 | A | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+9318T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956193 | |||||||
chr3:128956194 | AAT | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0188 others(25): Show |
29 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1353+9315_1353+931 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956194 | |||||||
chr3:128956196 | T | A | 2 | a0001c0001t0003g0214 a0013c0010t0001g0205 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1353+9315A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956196 | |||||||
chr3:128956196 | TA | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0125 others(26): Show |
30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1353+9314delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956196 | |||||||
chr3:128956198 | A | T | 2 | a0001c0001t0003g0214 a0013c0010t0001g0205 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1353+9313T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956198 | |||||||
chr3:128956199 | A | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1353+9312T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956199 | |||||||
chr3:128956200 | A | T | 3 | a0001c0001t0001g0196 a0001c0001t0005g0332 a0001c0001t0005g0333 |
3 | HG02280.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1353+9311T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956200 | |||||||
chr3:128956202 | A | T | 16 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(13): Show |
16 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9309T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956202 | |||||||
chr3:128956203 | A | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1353+9308T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956203 | |||||||
chr3:128956204 | A | T | 4 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0005c0005t0001g0014 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353+9307T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956204 | |||||||
chr3:128956207 | T | A | 25 | a0001c0001t0001g0013 a0001c0001t0001g0190 a0001c0001t0001g0193 others(22): Show |
25 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1353+9304A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956207 | |||||||
chr3:128956211 | A | T | 16 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(13): Show |
16 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9300T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956211 | |||||||
chr3:128956213 | A | T | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9298T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956213 | |||||||
chr3:128956215 | T | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0188 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9296A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956215 | |||||||
chr3:128956215 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+9296A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956215 | |||||||
chr3:128956215 | TA | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0155 others(3): Show |
7 | HG01081.hp2 HG01192.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353+9295delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956215 | |||||||
chr3:128956217 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18965.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1353+9294T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956217 | |||||||
chr3:128956220 | A | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+9291T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956220 | |||||||
chr3:128956223 | A | T | 11 | a0001c0001t0001g0045 a0001c0001t0001g0154 a0001c0001t0001g0158 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1353+9288T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956223 | |||||||
chr3:128956224 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0188 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9287T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956224 | |||||||
chr3:128956224 | AAAAAGAA others(3): Show |
A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+9277_1353+928 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956224 | |||||||
chr3:128956225 | A | G | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9286T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956225 | |||||||
chr3:128956229 | G | A | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9282C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956229 | |||||||
chr3:128956229 | G | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0188 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9282C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956229 | |||||||
chr3:128956230 | A | T | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9281T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956230 | |||||||
chr3:128956233 | AT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0188 others(30): Show |
34 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9277delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956233 | |||||||
chr3:128956234 | T | A | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9277A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956234 | |||||||
chr3:128956234 | T | TAAAA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(155): Show |
162 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1353+9276_1353+927 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956234 | |||||||
chr3:128956598 | G | GA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0248 a0001c0001t0001g0299 others(31): Show |
36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+8912dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956598 | |||||||
chr3:128956746 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1353+8765C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956746 | |||||||
chr3:128956837 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+8674T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956837 | |||||||
chr3:128956929 | A | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
83 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1353+8582T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956929 | |||||||
chr3:128956977 | C | CAAAA | 15 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(12): Show |
15 | HG00639.hp2 HG01167.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1353+8530_1353+853 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956977 | |||||||
chr3:128956977 | C | CAAAAA | 40 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0304 others(37): Show |
42 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1353+8529_1353+853 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956977 | |||||||
chr3:128956977 | C | CAAAAAA | 19 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(16): Show |
20 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1353+8528_1353+853 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956977 | |||||||
chr3:128956994 | A | AAAAAG | 6 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0128 others(3): Show |
6 | HG01175.hp1 HG02056.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+8516_1353+851 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | |||||||
chr3:128956994 | A | AAAAG | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1353+8513_1353+851 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | |||||||
chr3:128956994 | A | AAAG | 22 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0073 others(19): Show |
23 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1353+8516_1353+851 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | |||||||
chr3:128956994 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1353+8517T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | |||||||
chr3:128957037 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1353+8474C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957037 | |||||||
chr3:128957075 | T | G | 1 | a0001c0001t0001g0251 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1353+8436A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957075 | |||||||
chr3:128957258 | T | C | 20 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(17): Show |
20 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1353+8253A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957258 | |||||||
chr3:128957352 | AC | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(12): Show |
16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+8158delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957352 | |||||||
chr3:128957355 | A | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(12): Show |
16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+8156T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957355 | |||||||
chr3:128957423 | T | C | 2 | a0001c0001t0004g0273 a0001c0001t0004g0274 |
2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1353+8088A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957423 | |||||||
chr3:128957489 | A | T | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+8022T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957489 | |||||||
chr3:128957797 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1353+7714T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957797 | |||||||
chr3:128957832 | TG | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1353+7678delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957832 | |||||||
chr3:128957839 | G | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0109 others(32): Show |
37 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.1353+7672C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957839 | |||||||
chr3:128957915 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1353+7596G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957915 | |||||||
chr3:128958064 | T | C | 5 | a0001c0001t0001g0217 a0001c0001t0001g0258 a0001c0001t0001g0259 others(2): Show |
5 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+7447A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958064 | |||||||
chr3:128958255 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1353+7256T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958255 | |||||||
chr3:128958345 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1353+7166A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958345 | |||||||
chr3:128958669 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+6842C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958669 | |||||||
chr3:128958699 | A | G | 1 | a0012c0018t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1353+6812T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958699 | |||||||
chr3:128958748 | A | G | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+6763T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958748 | |||||||
chr3:128958770 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+6741C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958770 | |||||||
chr3:128958893 | CCT | C | 34 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(31): Show |
36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+6616_1353+661 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958893 | |||||||
chr3:128958998 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+6513C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958998 | |||||||
chr3:128959124 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1353+6387G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959124 | |||||||
chr3:128959128 | T | G | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+6383A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959128 | |||||||
chr3:128959456 | A | G | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+6055T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959456 | |||||||
chr3:128959495 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0113 |
3 | HG02735.hp1 HG04204.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1353+6016T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959495 | |||||||
chr3:128959614 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353+5897C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959614 | |||||||
chr3:128959628 | G | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
63 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1353+5883C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959628 | |||||||
chr3:128959753 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.1353+5758G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959753 | |||||||
chr3:128959834 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1353+5677G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959834 | |||||||
chr3:128959902 | T | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(17): Show |
21 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1353+5609A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959902 | |||||||
chr3:128960144 | C | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0299 others(31): Show |
36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+5367G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960144 | |||||||
chr3:128960160 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(15): Show |
18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353+5351C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960160 | |||||||
chr3:128960193 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1353+5318G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960193 | |||||||
chr3:128960406 | G | C | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+5105C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960406 | |||||||
chr3:128960439 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1353+5072T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960439 | |||||||
chr3:128960763 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(15): Show |
18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353+4748C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960763 | |||||||
chr3:128960772 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0003g0144 a0001c0001t0003g0145 others(15): Show |
18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353+4739G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960772 | |||||||
chr3:128960851 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0260 |
2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1353+4660C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960851 | |||||||
chr3:128960876 | T | C | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1353+4635A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960876 | |||||||
chr3:128960890 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1353+4621G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960890 | |||||||
chr3:128961036 | CAAG | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+4472_1353+447 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961036 | |||||||
chr3:128961284 | A | C | 8 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353+4227T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961284 | |||||||
chr3:128961312 | TC | T | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+4198delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961312 | |||||||
chr3:128961410 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1353+4101C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961410 | |||||||
chr3:128961415 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+4096T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961415 | |||||||
chr3:128961478 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1353+4033A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961478 | |||||||
chr3:128961499 | GT | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1353+4011delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961499 | |||||||
chr3:128961789 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+3722G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961789 | |||||||
chr3:128961793 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+3718G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961793 | |||||||
chr3:128961807 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1353+3704T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961807 | |||||||
chr3:128961924 | G | A | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+3587C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961924 | |||||||
chr3:128961928 | G | A | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+3583C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961928 | |||||||
chr3:128961932 | C | A | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+3579G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961932 | |||||||
chr3:128961959 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1353+3552G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961959 | |||||||
chr3:128961962 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1353+3549G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961962 | |||||||
chr3:128961986 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1353+3525C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961986 | |||||||
chr3:128962002 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1353+3509G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962002 | |||||||
chr3:128962019 | C | T | 2 | a0002c0002t0002g0298 a0002c0002t0002g0311 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1353+3492G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962019 | |||||||
chr3:128962039 | A | G | 1 | a0003c0004t0002g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1353+3472T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962039 | |||||||
chr3:128962058 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1353+3453G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962058 | |||||||
chr3:128962068 | C | G | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+3443G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962068 | |||||||
chr3:128962147 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1353+3364A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962147 | |||||||
chr3:128962259 | C | T | 30 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(27): Show |
30 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1353+3252G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962259 | |||||||
chr3:128962437 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1353+3074G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962437 | |||||||
chr3:128962442 | C | A | 52 | a0001c0001t0001g0007 a0001c0001t0001g0154 a0001c0001t0001g0158 others(49): Show |
54 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1353+3069G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962442 | |||||||
chr3:128962500 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02165.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1353+3011T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962500 | |||||||
chr3:128962561 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+2950C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962561 | |||||||
chr3:128962599 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1353+2912A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962599 | |||||||
chr3:128962837 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1353+2674T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962837 | |||||||
chr3:128962842 | C | T | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+2669G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962842 | |||||||
chr3:128962879 | T | C | 13 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(10): Show |
13 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.1353+2632A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962879 | |||||||
chr3:128962925 | T | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+2586A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962925 | |||||||
chr3:128962979 | C | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+2532G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962979 | |||||||
chr3:128962982 | G | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+2529C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962982 | |||||||
chr3:128962991 | G | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+2520C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962991 | |||||||
chr3:128963031 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1353+2480A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963031 | |||||||
chr3:128963096 | T | G | 6 | a0001c0001t0001g0253 a0001c0001t0003g0214 a0002c0002t0002g0298 others(3): Show |
6 | HG02129.hp1 HG02280.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+2415A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963096 | |||||||
chr3:128963214 | G | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0101 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1353+2297C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963214 | |||||||
chr3:128963241 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1353+2270G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963241 | |||||||
chr3:128963263 | A | C | 24 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0044 others(21): Show |
24 | HG00558.hp1 HG02071.hp1 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.1353+2248T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963263 | |||||||
chr3:128963274 | G | A | 14 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(11): Show |
14 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353+2237C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963274 | |||||||
chr3:128963278 | C | T | 15 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(12): Show |
15 | HG00558.hp1 HG02135.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1353+2233G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963278 | |||||||
chr3:128963279 | A | G | 15 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(12): Show |
15 | HG00558.hp1 HG02135.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1353+2232T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963279 | |||||||
chr3:128963284 | G | C | 24 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(21): Show |
24 | HG00558.hp1 HG01123.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1353+2227C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963284 | |||||||
chr3:128963326 | C | G | 1 | a0001c0001t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+2185G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963326 | |||||||
chr3:128963329 | A | G | 1 | a0001c0001t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+2182T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963329 | |||||||
chr3:128963333 | C | A | 1 | a0001c0001t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+2178G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963333 | |||||||
chr3:128963347 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1353+2164G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963347 | |||||||
chr3:128963355 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG01515.hp1 HG02300.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1353+2156C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963355 | |||||||
chr3:128963358 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+2153C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963358 | |||||||
chr3:128963374 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(11): Show |
15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1353+2137A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963374 | |||||||
chr3:128963382 | C | G | 7 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+2129G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963382 | |||||||
chr3:128963452 | C | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
60 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1353+2059G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963452 | |||||||
chr3:128963528 | C | T | 1 | a0001c0001t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+1983G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963528 | |||||||
chr3:128963533 | T | C | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+1978A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963533 | |||||||
chr3:128963539 | C | A | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | NA18946.hp2 NA18965.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1353+1972G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963539 | |||||||
chr3:128963540 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1353+1971A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963540 | |||||||
chr3:128963658 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG00558.hp1 HG02523.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1353+1853G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963658 | |||||||
chr3:128963673 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1353+1838G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963673 | |||||||
chr3:128963731 | C | G | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+1780G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963731 | |||||||
chr3:128963751 | C | T | 5 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(2): Show |
5 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+1760G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963751 | |||||||
chr3:128963776 | C | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1353+1735G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963776 | |||||||
chr3:128963860 | C | T | 7 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0136 others(4): Show |
7 | NA18747.hp2 NA18941.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+1651G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963860 | |||||||
chr3:128963998 | T | C | 1 | a0002c0002t0002g0008 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1353+1513A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963998 | |||||||
chr3:128964072 | C | T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353+1439G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964072 | |||||||
chr3:128964158 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0044 |
2 | NA19010.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1353+1353G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964158 | |||||||
chr3:128964239 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1353+1272T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964239 | |||||||
chr3:128964327 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+1184G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964327 | |||||||
chr3:128964450 | C | T | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+1061G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964450 | |||||||
chr3:128964631 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1353+880G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964631 | |||||||
chr3:128964641 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1353+870T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964641 | |||||||
chr3:128964642 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+869G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964642 | |||||||
chr3:128964793 | C | G | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+718G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964793 | |||||||
chr3:128964820 | C | T | 1 | a0016c0007t0001g0047 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1353+691G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964820 | |||||||
chr3:128964823 | T | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01255.hp2 HG01346.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+688A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964823 | |||||||
chr3:128964824 | G | A | 1 | a0015c0015t0001g0270 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1353+687C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964824 | |||||||
chr3:128964837 | C | T | 1 | a0001c0001t0008g0334 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1353+674G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964837 | |||||||
chr3:128964865 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1353+646C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964865 | |||||||
chr3:128965010 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+501G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965010 | |||||||
chr3:128965087 | C | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+424G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965087 | |||||||
chr3:128965392 | C | A | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+119G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965392 | |||||||
chr3:128965423 | G | T | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+88C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965423 | |||||||
chr3:128965475 | G | A | 2 | a0002c0002t0002g0323 a0002c0002t0002g0324 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1353+36C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965475 | |||||||
chr3:128965748 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0299 others(42): Show |
47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1169-53G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128965748 | |||||||
chr3:128965830 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1169-135T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128965830 | |||||||
chr3:128966099 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1169-404T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966099 | |||||||
chr3:128966214 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1169-519C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966214 | |||||||
chr3:128966221 | A | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA19076.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1169-526T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966221 | |||||||
chr3:128966568 | C | CT | 7 | a0001c0001t0001g0083 a0001c0001t0001g0137 a0002c0002t0002g0315 others(4): Show |
7 | HG02258.hp1 HG02683.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1169-874dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966568 | |||||||
chr3:128966568 | CT | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0135 a0001c0003t0001g0150 others(11): Show |
14 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1169-874delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966568 | |||||||
chr3:128966571 | T | TC | 11 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1169-877_1169-876i others(3): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966571 | |||||||
chr3:128966572 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0005g0332 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169-877A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966572 | |||||||
chr3:128966573 | T | TC | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(35): Show |
40 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1169-879_1169-878i others(3): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966573 | |||||||
chr3:128966574 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1169-879A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966574 | |||||||
chr3:128966575 | T | C | 1 | a0012c0018t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1169-880A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966575 | |||||||
chr3:128966633 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1169-938G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966633 | |||||||
chr3:128966738 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1169-1043A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966738 | |||||||
chr3:128966835 | G | A | 4 | a0001c0003t0001g0210 a0001c0003t0001g0211 a0001c0003t0001g0212 others(1): Show |
4 | HG00639.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169-1140C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966835 | |||||||
chr3:128966918 | A | C | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1169-1223T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966918 | |||||||
chr3:128967062 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1169-1367T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967062 | |||||||
chr3:128967093 | T | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1169-1398A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967093 | |||||||
chr3:128967156 | C | CA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1169-1462dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967156 | |||||||
chr3:128967238 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1169-1543G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967238 | |||||||
chr3:128967657 | G | A | 1 | a0001c0001t0007g0080 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1169-1962C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967657 | |||||||
chr3:128967677 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1169-1982C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967677 | |||||||
chr3:128967702 | C | CA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
71 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1169-2008dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967702 | |||||||
chr3:128967702 | C | CAA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(31): Show |
36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1169-2009_1169-200 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967702 | |||||||
chr3:128967703 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1169-2008T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967703 | |||||||
chr3:128967741 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1169-2046G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967741 | |||||||
chr3:128967861 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1169-2166T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967861 | |||||||
chr3:128967978 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1169-2283T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967978 | |||||||
chr3:128968069 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1169-2374T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968069 | |||||||
chr3:128968078 | CA | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1169-2384delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968078 | |||||||
chr3:128968156 | A | G | 1 | a0001c0001t0004g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1169-2461T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968156 | |||||||
chr3:128968193 | T | C | 1 | a0012c0018t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1169-2498A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968193 | |||||||
chr3:128968354 | A | C | 2 | a0002c0002t0002g0323 a0002c0002t0002g0324 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1169-2659T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968354 | |||||||
chr3:128968597 | T | TA | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1168+2689dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968597 | |||||||
chr3:128968612 | G | A | 2 | a0002c0002t0002g0316 a0002c0002t0002g0321 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1168+2675C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968612 | |||||||
chr3:128968736 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1168+2551T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968736 | |||||||
chr3:128968765 | G | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0299 others(42): Show |
47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1168+2522C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968765 | |||||||
chr3:128968785 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1168+2502C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968785 | |||||||
chr3:128968810 | T | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0299 others(42): Show |
47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1168+2477A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968810 | |||||||
chr3:128968845 | C | T | 3 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 |
3 | HG02055.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168+2442G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968845 | |||||||
chr3:128968846 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1168+2441C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968846 | |||||||
chr3:128968901 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG01167.hp1 HG01175.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168+2386A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968901 | |||||||
chr3:128968937 | G | A | 1 | a0002c0002t0002g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1168+2350C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968937 | |||||||
chr3:128969073 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1168+2214T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969073 | |||||||
chr3:128969218 | A | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1168+2069T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969218 | |||||||
chr3:128969227 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+2060A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969227 | |||||||
chr3:128969238 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0127 |
2 | NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1168+2049G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969238 | |||||||
chr3:128969247 | GCTGA | G | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+2036_1168+203 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969247 | |||||||
chr3:128969370 | A | G | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1168+1917T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969370 | |||||||
chr3:128969475 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1168+1812T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969475 | |||||||
chr3:128969522 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+1765C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969522 | |||||||
chr3:128969572 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1168+1715G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969572 | |||||||
chr3:128969573 | G | A | 1 | a0003c0004t0002g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1168+1714C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969573 | |||||||
chr3:128969573 | GA | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+1713delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969573 | |||||||
chr3:128969656 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+1631G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969656 | |||||||
chr3:128969697 | C | T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
8 | HG02602.hp2 NA18747.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168+1590G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969697 | |||||||
chr3:128969700 | A | G | 1 | a0001c0001t0007g0080 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1168+1587T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969700 | |||||||
chr3:128969719 | G | A | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1168+1568C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969719 | |||||||
chr3:128969745 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+1542A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969745 | |||||||
chr3:128969791 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+1496A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969791 | |||||||
chr3:128969805 | G | A | 9 | a0001c0003t0001g0150 a0001c0003t0001g0206 a0001c0003t0001g0207 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168+1482C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969805 | |||||||
chr3:128970086 | C | T | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+1201G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970086 | |||||||
chr3:128970241 | C | CA | 19 | a0001c0001t0001g0013 a0001c0001t0001g0257 a0001c0001t0003g0144 others(16): Show |
19 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1168+1045dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970241 | |||||||
chr3:128970474 | C | CA | 5 | a0001c0001t0001g0157 a0001c0001t0001g0257 a0001c0001t0003g0144 others(2): Show |
5 | HG01433.hp2 HG01978.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168+812dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970474 | |||||||
chr3:128970504 | T | TA | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1168+782dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970504 | |||||||
chr3:128970541 | T | C | 1 | a0001c0001t0005g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1168+746A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970541 | |||||||
chr3:128970648 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1168+639T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970648 | |||||||
chr3:128970811 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | NA18946.hp2 NA18965.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1168+476G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970811 | |||||||
chr3:128970870 | G | A | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+417C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970870 | |||||||
chr3:128971076 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1168+211G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128971076 | |||||||
chr3:128971584 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0125 |
2 | HG02148.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1022-151T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971584 | |||||||
chr3:128971618 | C | T | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-185G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971618 | |||||||
chr3:128971870 | C | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-437G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971870 | |||||||
chr3:128971907 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1022-474G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971907 | |||||||
chr3:128971982 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0111 |
2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1022-549C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971982 | |||||||
chr3:128972105 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.1022-672G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972105 | |||||||
chr3:128972247 | C | CTT | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-816_1022-815d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972247 | |||||||
chr3:128972309 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1022-876C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972309 | |||||||
chr3:128972414 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-981C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972414 | |||||||
chr3:128972418 | T | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1022-985A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972418 | |||||||
chr3:128972467 | C | G | 7 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG00423.hp2 HG00558.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-1034G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972467 | |||||||
chr3:128972521 | T | C | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1022-1088A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972521 | |||||||
chr3:128972564 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
244 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1022-1131C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972564 | |||||||
chr3:128972574 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-1141C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972574 | |||||||
chr3:128972636 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
116 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.1022-1203C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972636 | |||||||
chr3:128972749 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-1316C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972749 | |||||||
chr3:128972812 | G | A | 1 | a0002c0002t0002g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1022-1379C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972812 | |||||||
chr3:128972936 | C | T | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1022-1503G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972936 | |||||||
chr3:128972973 | G | A | 1 | a0004c0006t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1022-1540C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972973 | |||||||
chr3:128973098 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1022-1665A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973098 | |||||||
chr3:128973518 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-2085A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973518 | |||||||
chr3:128973546 | C | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1022-2113G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973546 | |||||||
chr3:128973610 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1021+2169G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973610 | |||||||
chr3:128973659 | G | GA | 17 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0125 others(14): Show |
17 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1021+2119dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973659 | |||||||
chr3:128973659 | GA | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1021+2119delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973659 | |||||||
chr3:128973912 | T | C | 4 | a0001c0001t0001g0218 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1867A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973912 | |||||||
chr3:128973921 | T | C | 1 | a0002c0002t0002g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1021+1858A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973921 | |||||||
chr3:128974039 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1021+1740C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974039 | |||||||
chr3:128974069 | A | C | 1 | a0001c0014t0001g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1021+1710T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974069 | |||||||
chr3:128974350 | C | T | 1 | a0004c0006t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021+1429G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974350 | |||||||
chr3:128974611 | AG | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1021+1167delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974611 | |||||||
chr3:128974764 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1021+1015A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974764 | |||||||
chr3:128974778 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1021+1001C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974778 | |||||||
chr3:128974877 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
36 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1021+902A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974877 | |||||||
chr3:128974962 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0299 others(42): Show |
47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1021+817G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974962 | |||||||
chr3:128974976 | C | G | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0294 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1021+803G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974976 | |||||||
chr3:128974989 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1021+790C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974989 | |||||||
chr3:128975064 | G | C | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+715C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975064 | |||||||
chr3:128975123 | AAAAAT | A | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021+651_1021+655d others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975123 | |||||||
chr3:128975128 | T | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0122 |
2 | HG03688.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1021+651A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975128 | |||||||
chr3:128975231 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1021+548T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975231 | |||||||
chr3:128975426 | G | GGGAT | 4 | a0001c0001t0001g0059 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG01943.hp2 HG02602.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021+349_1021+352d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | |||||||
chr3:128975426 | GGGAT | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(118): Show |
123 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1021+349_1021+352d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | |||||||
chr3:128975426 | GGGATGGA others(1): Show |
G | 51 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0038 others(48): Show |
53 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.1021+345_1021+352d others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | |||||||
chr3:128975426 | GGGATGGA others(9): Show |
G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
60 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1021+337_1021+352d others(18): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | |||||||
chr3:128975426 | GGGATGGA others(17): Show |
G | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+329_1021+352d others(26): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | |||||||
chr3:128975457 | A | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021+322T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975457 | |||||||
chr3:128975577 | T | C | 1 | a0002c0002t0002g0315 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1021+202A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975577 | |||||||
chr3:128976190 | A | C | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.897-287T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976190 | |||||||
chr3:128976205 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.897-302A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976205 | |||||||
chr3:128976253 | T | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG01069.hp1 HG01109.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.897-350A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976253 | |||||||
chr3:128976788 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0116 others(18): Show |
21 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.896+191A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976788 | |||||||
chr3:128976869 | G | A | 2 | a0001c0001t0001g0130 a0009c0013t0002g0143 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.896+110C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976869 | |||||||
chr3:128976966 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
20 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.896+13C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976966 | |||||||
chr3:128977184 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.809-118T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977184 | |||||||
chr3:128977355 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.809-289T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977355 | |||||||
chr3:128977511 | C | T | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.809-445G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977511 | |||||||
chr3:128977675 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.808+370T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977675 | |||||||
chr3:128977689 | T | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0116 others(12): Show |
15 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.808+356A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977689 | |||||||
chr3:128977723 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
63 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.808+322C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977723 | |||||||
chr3:128977732 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.808+313C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977732 | |||||||
chr3:128977751 | C | T | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.808+294G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977751 | |||||||
chr3:128977816 | G | A | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.808+229C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977816 | |||||||
chr3:128977838 | G | A | 2 | a0002c0002t0002g0316 a0002c0002t0002g0321 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.808+207C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977838 | |||||||
chr3:128978242 | AT | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0299 others(42): Show |
47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.668-58delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978242 | |||||||
chr3:128978361 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-176A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978361 | |||||||
chr3:128978470 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.668-285C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978470 | |||||||
chr3:128978565 | C | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-380G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978565 | |||||||
chr3:128978661 | A | T | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-476T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978661 | |||||||
chr3:128978832 | C | G | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-647G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978832 | |||||||
chr3:128978971 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.668-786T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978971 | |||||||
chr3:128979408 | A | T | 1 | a0002c0002t0002g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.668-1223T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979408 | |||||||
chr3:128979484 | G | A | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-1299C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979484 | |||||||
chr3:128979546 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0111 |
2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.668-1361G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979546 | |||||||
chr3:128979718 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.668-1533C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979718 | |||||||
chr3:128979776 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.668-1591T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979776 | |||||||
chr3:128979812 | G | A | 1 | a0004c0006t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.668-1627C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979812 | |||||||
chr3:128979836 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.668-1651A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979836 | |||||||
chr3:128979852 | C | T | 1 | a0002c0002t0002g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.668-1667G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979852 | |||||||
chr3:128979866 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.668-1681A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979866 | |||||||
chr3:128979923 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.668-1738C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979923 | |||||||
chr3:128979944 | AATAATAT | A | 4 | a0002c0002t0002g0317 a0002c0002t0002g0318 a0002c0002t0002g0319 others(1): Show |
4 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-1766_668-1760d others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979944 | |||||||
chr3:128979946 | TA | T | 27 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(24): Show |
29 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.668-1762delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979946 | |||||||
chr3:128979947 | A | AAT | 13 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0001t0001g0115 others(10): Show |
13 | HG00642.hp2 HG01069.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.668-1764_668-1763d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979947 | A | AATAATAT others(4): Show |
1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-1763_668-1762i others(13): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979947 | A | AATAT | 63 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0056 others(60): Show |
64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.668-1766_668-1763d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979947 | A | AATATAT | 18 | a0001c0001t0001g0089 a0001c0001t0001g0109 a0001c0001t0001g0125 others(15): Show |
18 | HG00609.hp2 HG00639.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.668-1768_668-1763d others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979947 | A | AATATATA others(1): Show |
4 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0001g0081 others(1): Show |
4 | HG01943.hp1 HG02165.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-1770_668-1763d others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979947 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0059 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.668-1772_668-1763d others(12): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979947 | AATAT | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
37 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.668-1766_668-1763d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979947 | AATATAT | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
60 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.668-1768_668-1763d others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | |||||||
chr3:128979973 | A | T | 1 | a0007c0012t0001g0054 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.668-1788T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979973 | |||||||
chr3:128980366 | C | CA | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0113 others(5): Show |
8 | HG01175.hp1 HG01928.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.668-2182dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | |||||||
chr3:128980366 | CA | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.668-2182delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | |||||||
chr3:128980366 | CAA | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0020 others(47): Show |
52 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.668-2183_668-2182d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | |||||||
chr3:128980366 | CAAA | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0115 others(41): Show |
46 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.668-2184_668-2182d others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | |||||||
chr3:128980524 | T | A | 1 | a0001c0001t0001g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.668-2339A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980524 | |||||||
chr3:128980563 | G | A | 2 | a0002c0002t0002g0323 a0002c0002t0002g0324 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.668-2378C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980563 | |||||||
chr3:128980916 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.668-2731A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980916 | |||||||
chr3:128981038 | C | CT | 9 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0115 others(6): Show |
9 | HG01934.hp2 HG02074.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.668-2854dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981038 | |||||||
chr3:128981090 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.668-2905C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981090 | |||||||
chr3:128981181 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0152 others(30): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-2996G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981181 | |||||||
chr3:128981197 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.668-3012G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981197 | |||||||
chr3:128981252 | C | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0197 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.668-3067G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981252 | |||||||
chr3:128981274 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.668-3089C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981274 | |||||||
chr3:128981683 | C | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.668-3498G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981683 | |||||||
chr3:128981890 | C | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
63 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.668-3705G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981890 | |||||||
chr3:128982023 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.668-3838T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982023 | |||||||
chr3:128982084 | G | C | 1 | a0001c0001t0001g0005 | 2 | NA18943.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.668-3899C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982084 | |||||||
chr3:128982127 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-3942G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982127 | |||||||
chr3:128982222 | C | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00558.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.668-4037G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982222 | |||||||
chr3:128982248 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.668-4063G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982248 | |||||||
chr3:128982287 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.668-4102A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982287 | |||||||
chr3:128982487 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-4302C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982487 | |||||||
chr3:128982531 | G | A | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-4346C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982531 | |||||||
chr3:128982611 | A | G | 1 | a0014c0019t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.668-4426T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982611 | |||||||
chr3:128982624 | G | A | 1 | a0013c0010t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-4439C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982624 | |||||||
chr3:128982645 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.668-4460A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982645 | |||||||
chr3:128982662 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.668-4477A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982662 | |||||||
chr3:128982797 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0008g0334 |
2 | HG01175.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.668-4612C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982797 | |||||||
chr3:128983030 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.667+4586C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983030 | |||||||
chr3:128983038 | T | C | 4 | a0001c0001t0001g0053 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG00323.hp2 HG01943.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+4578A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983038 | |||||||
chr3:128983406 | C | G | 1 | a0001c0001t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.667+4210G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983406 | |||||||
chr3:128983661 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667+3955A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983661 | |||||||
chr3:128983904 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.667+3712G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983904 | |||||||
chr3:128983954 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.667+3662C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983954 | |||||||
chr3:128984024 | G | T | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+3592C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984024 | |||||||
chr3:128984050 | CGGGGGAC others(18): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.667+3541_667+3565d others(27): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984050 | |||||||
chr3:128984173 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.667+3443G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984173 | |||||||
chr3:128984425 | C | T | 1 | a0012c0018t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.667+3191G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984425 | |||||||
chr3:128984524 | C | T | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+3092G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984524 | |||||||
chr3:128984566 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0043 |
2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.667+3050G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984566 | |||||||
chr3:128984633 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.667+2983C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984633 | |||||||
chr3:128984748 | A | G | 2 | a0001c0001t0004g0273 a0001c0001t0004g0274 |
2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.667+2868T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984748 | |||||||
chr3:128984825 | T | A | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.667+2791A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984825 | |||||||
chr3:128984859 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
110 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.667+2757C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984859 | |||||||
chr3:128984909 | A | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.667+2707T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984909 | |||||||
chr3:128985447 | A | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.667+2169T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128985447 | |||||||
chr3:128985757 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0156 |
4 | HG01081.hp2 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1859G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128985757 | |||||||
chr3:128986037 | C | A | 1 | a0009c0013t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.667+1579G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986037 | |||||||
chr3:128986048 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.667+1568T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986048 | |||||||
chr3:128986168 | T | C | 6 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | HG00639.hp1 HG01516.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.667+1448A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986168 | |||||||
chr3:128986192 | C | T | 5 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(2): Show |
5 | HG03471.hp1 NA18747.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+1424G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986192 | |||||||
chr3:128986193 | G | A | 1 | a0006c0017t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.667+1423C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986193 | |||||||
chr3:128986240 | CT | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
63 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.667+1375delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986240 | |||||||
chr3:128986396 | T | C | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.667+1220A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986396 | |||||||
chr3:128986471 | TC | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.667+1144delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986471 | |||||||
chr3:128986724 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
244 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.667+892C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986724 | |||||||
chr3:128986737 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0005g0332 a0001c0001t0005g0333 |
3 | HG02280.hp2 HG02293.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.667+879C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986737 | |||||||
chr3:128986741 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.667+875C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986741 | |||||||
chr3:128987030 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.667+586C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987030 | |||||||
chr3:128987161 | G | A | 6 | a0003c0004t0002g0180 a0003c0004t0002g0181 a0003c0004t0002g0182 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+455C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987161 | |||||||
chr3:128987240 | A | G | 1 | a0001c0001t0005g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.667+376T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987240 | |||||||
chr3:128987311 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.667+305A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987311 | |||||||
chr3:128987861 | G | A | 1 | a0001c0001t0001g0005 | 2 | NA18943.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.454-32C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987861 | |||||||
chr3:128987873 | G | A | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.454-44C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987873 | |||||||
chr3:128987882 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.454-53C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987882 | |||||||
chr3:128987930 | G | A | 2 | a0005c0005t0001g0014 a0005c0005t0001g0015 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.454-101C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987930 | |||||||
chr3:128988139 | ACACACAT others(15): Show |
A | 1 | a0001c0016t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.454-332_454-311del others(22): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988139 | |||||||
chr3:128988157 | G | A | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.454-328C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988157 | |||||||
chr3:128988269 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.454-440C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988269 | |||||||
chr3:128988279 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.453+449C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988279 | |||||||
chr3:128988517 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(17): Show |
21 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.453+211C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988517 | |||||||
chr3:128988545 | A | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+183T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988545 | |||||||
chr3:128988631 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.453+97C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988631 | |||||||
chr3:128989289 | T | TA | 7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG01175.hp1 HG01928.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-372dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | |||||||
chr3:128989289 | TA | T | 23 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(20): Show |
23 | HG01928.hp1 HG01943.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.263-372delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | |||||||
chr3:128989289 | TAA | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.263-373_263-372del others(2): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | |||||||
chr3:128989289 | TAAA | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0151 others(19): Show |
23 | HG01070.hp1 HG01884.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.263-374_263-372del others(3): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | |||||||
chr3:128989289 | TAAAA | T | 7 | a0001c0001t0001g0141 a0001c0001t0003g0144 a0001c0001t0003g0145 others(4): Show |
7 | HG01123.hp2 HG01255.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-375_263-372del others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | |||||||
chr3:128989571 | C | T | 1 | a0001c0001t0004g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.263-653G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989571 | |||||||
chr3:128989602 | C | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.263-684G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989602 | |||||||
chr3:128989711 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
244 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.263-793C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989711 | |||||||
chr3:128989844 | AGCAT | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0186 |
3 | HG01261.hp1 HG01433.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.263-930_263-927del others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989844 | |||||||
chr3:128990280 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.263-1362A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990280 | |||||||
chr3:128990465 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.263-1547G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990465 | |||||||
chr3:128990483 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.263-1565T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990483 | |||||||
chr3:128990634 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02602.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.263-1716C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990634 | |||||||
chr3:128990714 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.263-1796C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990714 | |||||||
chr3:128990838 | A | C | 1 | a0001c0003t0001g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.263-1920T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990838 | |||||||
chr3:128990923 | T | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(13): Show |
17 | HG00642.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.263-2005A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990923 | |||||||
chr3:128990963 | T | C | 1 | a0002c0002t0002g0326 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.263-2045A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990963 | |||||||
chr3:128990979 | T | A | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-2061A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990979 | |||||||
chr3:128991120 | C | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.262+1923G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991120 | |||||||
chr3:128991137 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.262+1906A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991137 | |||||||
chr3:128991176 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
63 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.262+1867C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991176 | |||||||
chr3:128991187 | A | C | 3 | a0004c0006t0001g0329 a0004c0006t0001g0330 a0004c0021t0001g0328 |
3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.262+1856T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991187 | |||||||
chr3:128991210 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.262+1833G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991210 | |||||||
chr3:128991228 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0295 |
3 | HG01081.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.262+1815C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991228 | |||||||
chr3:128991257 | G | T | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+1786C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991257 | |||||||
chr3:128991702 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.262+1341C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991702 | |||||||
chr3:128991862 | A | T | 2 | a0001c0003t0001g0150 a0001c0003t0001g0206 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.262+1181T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991862 | |||||||
chr3:128991870 | G | A | 1 | a0012c0018t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.262+1173C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991870 | |||||||
chr3:128991912 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.262+1131A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991912 | |||||||
chr3:128991922 | A | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
20 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.262+1121T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991922 | |||||||
chr3:128991927 | G | A | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+1116C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991927 | |||||||
chr3:128992175 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+868C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992175 | |||||||
chr3:128992290 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | NA18747.hp2 NA18941.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+753C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992290 | |||||||
chr3:128992445 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0141 others(44): Show |
49 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.262+598G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992445 | |||||||
chr3:128992487 | G | A | 12 | a0001c0001t0001g0013 a0001c0003t0001g0150 a0001c0003t0001g0206 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+556C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992487 | |||||||
chr3:128992571 | G | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 |
3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.262+472C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992571 | |||||||
chr3:128992575 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262+468A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992575 | |||||||
chr3:128992581 | T | TA | 13 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(10): Show |
13 | HG01123.hp2 HG01255.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.262+461_262+462ins others(1): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992581 | |||||||
chr3:128992582 | T | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.262+461A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992582 | |||||||
chr3:128992583 | T | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+460A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992583 | |||||||
chr3:128992585 | T | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.262+458A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992585 | |||||||
chr3:128992645 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0304 others(30): Show |
35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.262+398C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992645 | |||||||
chr3:128992755 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.262+288T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992755 | |||||||
chr3:128992766 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+277A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992766 | |||||||
chr3:128992768 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+275A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992768 | |||||||
chr3:128992771 | ATGGTTTT others(6): Show |
A | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+259_262+271del others(13): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992771 | |||||||
chr3:128992788 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+255A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992788 | |||||||
chr3:128992789 | G | T | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+254C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992789 | |||||||
chr3:128992868 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+175C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992868 | |||||||
chr3:128992869 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+174G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992869 | |||||||
chr3:128992870 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+173G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992870 | |||||||
chr3:128992872 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+171G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992872 | |||||||
chr3:128992876 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+167A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992876 | |||||||
chr3:128992878 | A | C | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+165T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992878 | |||||||
chr3:128992880 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+163T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992880 | |||||||
chr3:128992881 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+162A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992881 | |||||||
chr3:128992882 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+161A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992882 | |||||||
chr3:128992886 | G | T | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+157C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992886 | |||||||
chr3:128992887 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+156A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992887 | |||||||
chr3:128992970 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.262+73G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992970 | |||||||
chr3:128993368 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-32-32G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993368 | |||||||
chr3:128993535 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
36 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32-199T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993535 | |||||||
chr3:128993587 | C | T | 3 | a0001c0001t0001g0013 a0005c0005t0001g0014 a0005c0005t0001g0015 |
3 | HG01069.hp1 HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-32-251G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993587 | |||||||
chr3:128993689 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+291G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993689 | |||||||
chr3:128993763 | G | C | 1 | a0001c0001t0001g0331 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-33+217C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993763 | |||||||
chr3:128993931 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-33+49C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993931 |