Item | Value |
---|---|
geneid | 89876 |
ensemblid | ENSG00000183833.16 |
hgncid | 24010 |
symbol | CFAP91 |
name | cilia and flagella associated protein 91 |
refseq_nuc | NM_033364.4 |
refseq_prot | NP_203528.3 |
ensembl_nuc | ENST00000273390.9 |
ensembl_prot | ENSP00000273390.5 |
mane_status | MANE Select |
chr | chr3 |
start | 119703022 |
end | 119767102 |
strand | + |
ver | v1.2 |
region | chr3:119703022-119767102 |
region5000 | chr3:119698022-119772102 |
regionname0 | CFAP91_chr3_119703022_119767102 |
regionname5000 | CFAP91_chr3_119698022_119772102 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 767 | 316 | 43 | 59 | 160 | 14 | 39 | 123 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0002 | 1/0 | 767 | 21 | 19 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0003 | 0/0 | 767 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0004 | 0/0 | 767 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0005 | 0/0 | 767 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0006 | 0/0 | 767 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0007 | 0/0 | 766 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(761): Show |
chr3 | 119698022 | 119772102 |
a0008 | 0/0 | 767 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0009 | 0/0 | 767 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0010 | 0/0 | 767 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0011 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0012 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0013 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0014 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0015 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0016 | 0/0 | 767 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0017 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
a0018 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | MSHAV others(762): Show |
chr3 | 119698022 | 119772102 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2301 | 207 | 19 | 34 | 117 | 9 | 27 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0001c0002 | 0/0 | 2301 | 71 | 3 | 16 | 43 | 3 | 6 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0001c0003 | 0/0 | 2301 | 21 | 11 | 8 | 0 | 2 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0001c0007 | 0/0 | 2301 | 7 | 5 | 0 | 0 | 0 | 2 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0001c0009 | 0/0 | 2301 | 5 | 4 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0001c0013 | 0/0 | 2301 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0001c0014 | 0/0 | 2301 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0001c0023 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0002c0004 | 1/0 | 2301 | 21 | 19 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0003c0005 | 0/0 | 2301 | 11 | 9 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0003c0027 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0004c0006 | 0/0 | 2301 | 7 | 0 | 0 | 7 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0005c0008 | 0/0 | 2301 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0006c0010 | 0/0 | 2301 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0007c0011 | 0/0 | 2298 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2293): Show |
chr3 | 119698022 | 119772102 | ||
a0008c0012 | 0/0 | 2301 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0009c0022 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0009c0026 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0010c0015 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0010c0021 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0011c0028 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0012c0017 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0013c0020 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0014c0024 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0015c0025 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0016c0018 | 0/0 | 2301 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0017c0016 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 | ||
a0018c0019 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | ATGAG others(2296): Show |
chr3 | 119698022 | 119772102 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4433 | 187 | 14 | 29 | 109 | 9 | 25 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0003 | 0/0 | 4433 | 7 | 0 | 0 | 7 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0004 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4435): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0011 | 0/0 | 4429 | 3 | 0 | 3 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4424): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0012 | 0/0 | 4433 | 3 | 0 | 2 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0024 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0025 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0027 | 0/0 | 4433 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0001t0030 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0002 | 0/0 | 4433 | 57 | 1 | 14 | 34 | 2 | 6 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0003 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0006 | 0/0 | 4433 | 7 | 0 | 0 | 6 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0013 | 0/0 | 4433 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0019 | 0/0 | 4433 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0020 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0021 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0002t0022 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0003t0001 | 0/0 | 4433 | 4 | 2 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0003t0003 | 0/0 | 4433 | 13 | 5 | 6 | 0 | 2 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0003t0004 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4435): Show |
chr3 | 119698022 | 119772102 |
a0001c0003t0018 | 0/0 | 4433 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0003t0029 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0007t0008 | 0/0 | 4433 | 7 | 5 | 0 | 0 | 0 | 2 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0009t0001 | 0/0 | 4433 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0009t0005 | 0/0 | 4433 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0013t0015 | 0/0 | 4433 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0013t0028 | 0/0 | 4433 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0014t0016 | 0/0 | 4433 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0001c0023t0015 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0002c0004t0001 | 1/0 | 4433 | 8 | 7 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0002c0004t0004 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4435): Show |
chr3 | 119698022 | 119772102 |
a0002c0004t0005 | 0/0 | 4433 | 11 | 10 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0003c0005t0004 | 0/0 | 4440 | 11 | 9 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4435): Show |
chr3 | 119698022 | 119772102 |
a0003c0027t0031 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4435): Show |
chr3 | 119698022 | 119772102 |
a0004c0006t0001 | 0/0 | 4433 | 7 | 0 | 0 | 7 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0005c0008t0007 | 0/0 | 4433 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0006c0010t0014 | 0/0 | 4433 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0006c0010t0017 | 0/0 | 4433 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0006c0010t0033 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0007c0011t0009 | 0/0 | 4430 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4425): Show |
chr3 | 119698022 | 119772102 |
a0008c0012t0010 | 0/0 | 4433 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0009c0022t0005 | 0/0 | 4433 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0009c0026t0032 | 0/0 | 4433 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0010c0015t0007 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0010c0021t0007 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0011c0028t0006 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0012c0017t0023 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0013c0020t0026 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0014c0024t0005 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0015c0025t0010 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0016c0018t0001 | 0/0 | 4433 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0017c0016t0001 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
a0018c0019t0001 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | GTTAC others(4428): Show |
chr3 | 119698022 | 119772102 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0011g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0011g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0011g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0012g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0012g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0024g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0025g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0027g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0001t0030g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0013g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0019g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0020g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0021g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0002t0022g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0018g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0018g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0003t0029g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0007t0008g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0007t0008g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0007t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0007t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0007t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0009t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0009t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0009t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0009t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0013t0015g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0013t0028g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0014t0016g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0014t0016g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0001c0023t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0001g0003 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0002c0004t0005g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0005t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0003c0027t0031g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0004c0006t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0004c0006t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0004c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0004c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0004c0006t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0004c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0005c0008t0007g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0005c0008t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0005c0008t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0005c0008t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0006c0010t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0006c0010t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0006c0010t0017g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0006c0010t0017g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0006c0010t0033g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0007c0011t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0007c0011t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0007c0011t0009g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0007c0011t0009g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0008c0012t0010g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0008c0012t0010g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0008c0012t0010g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0009c0022t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0009c0026t0032g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0010c0015t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0010c0021t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0011c0028t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0012c0017t0023g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0013c0020t0026g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0014c0024t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0015c0025t0010g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0016c0018t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0017c0016t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
a0018c0019t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0061 | EUR | GBR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00280 | hp2 | a0001 | c0003 | t0003 | g0323 | EUR | FIN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00423 | hp2 | a0004 | c0006 | t0001 | g0019 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00544 | hp2 | a0001 | c0002 | t0006 | g0088 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00597 | hp1 | a0007 | c0011 | t0009 | g0247 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00621 | hp1 | a0011 | c0028 | t0006 | g0083 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00639 | hp1 | a0002 | c0004 | t0005 | g0343 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0330 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00735 | hp2 | a0001 | c0002 | t0013 | g0104 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0328 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00741 | hp1 | a0001 | c0003 | t0003 | g0027 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01069 | hp1 | a0001 | c0001 | t0011 | g0298 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01070 | hp1 | a0001 | c0001 | t0012 | g0123 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01071 | hp1 | a0001 | c0001 | t0012 | g0124 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01074 | hp1 | a0001 | c0002 | t0019 | g0051 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01099 | hp2 | a0003 | c0005 | t0004 | g0319 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01106 | hp1 | a0001 | c0001 | t0011 | g0300 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01106 | hp2 | a0003 | c0005 | t0004 | g0315 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01109 | hp1 | a0001 | c0003 | t0003 | g0321 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01109 | hp2 | a0009 | c0022 | t0005 | g0324 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01243 | hp1 | a0001 | c0003 | t0003 | g0327 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01257 | hp1 | a0001 | c0003 | t0003 | g0025 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01258 | hp1 | a0001 | c0003 | t0003 | g0025 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01433 | hp1 | a0001 | c0003 | t0003 | g0027 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01433 | hp2 | a0009 | c0026 | t0032 | g0099 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0065 | EUR | IBS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01517 | hp2 | a0001 | c0003 | t0003 | g0320 | EUR | IBS | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01884 | hp1 | a0012 | c0017 | t0023 | g0168 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01884 | hp2 | a0001 | c0003 | t0004 | g0303 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01891 | hp1 | a0006 | c0010 | t0017 | g0036 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01891 | hp2 | a0001 | c0007 | t0008 | g0005 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02015 | hp1 | a0001 | c0002 | t0006 | g0074 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02055 | hp2 | a0001 | c0003 | t0018 | g0333 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02145 | hp1 | a0013 | c0020 | t0026 | g0106 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CDX | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02257 | hp1 | a0003 | c0005 | t0004 | g0307 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02258 | hp1 | a0010 | c0015 | t0007 | g0159 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02258 | hp2 | a0002 | c0004 | t0001 | g0003 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02280 | hp1 | a0001 | c0009 | t0005 | g0105 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02280 | hp2 | a0003 | c0005 | t0004 | g0306 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02300 | hp2 | a0001 | c0001 | t0011 | g0297 | AMR | PEL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02451 | hp2 | a0001 | c0002 | t0013 | g0048 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02572 | hp1 | a0003 | c0005 | t0004 | g0317 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02572 | hp2 | a0001 | c0003 | t0018 | g0332 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02602 | hp1 | a0001 | c0013 | t0028 | g0185 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02615 | hp1 | a0005 | c0008 | t0007 | g0004 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02615 | hp2 | a0002 | c0004 | t0005 | g0336 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02622 | hp1 | a0008 | c0012 | t0010 | g0310 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02622 | hp2 | a0001 | c0007 | t0008 | g0033 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02630 | hp1 | a0003 | c0005 | t0004 | g0314 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02630 | hp2 | a0001 | c0007 | t0008 | g0005 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02698 | hp2 | a0001 | c0014 | t0016 | g0109 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02717 | hp1 | a0002 | c0004 | t0001 | g0347 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02717 | hp2 | a0002 | c0004 | t0005 | g0029 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0304 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02723 | hp2 | a0005 | c0008 | t0007 | g0351 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02809 | hp1 | a0002 | c0004 | t0005 | g0346 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02809 | hp2 | a0002 | c0004 | t0001 | g0344 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02818 | hp1 | a0002 | c0004 | t0005 | g0345 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02818 | hp2 | a0003 | c0005 | t0004 | g0111 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02896 | hp1 | a0001 | c0009 | t0001 | g0107 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02922 | hp1 | a0002 | c0004 | t0005 | g0029 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02922 | hp2 | a0003 | c0005 | t0004 | g0334 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02965 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02965 | hp2 | a0010 | c0021 | t0007 | g0308 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02970 | hp1 | a0002 | c0004 | t0005 | g0340 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02976 | hp1 | a0001 | c0007 | t0008 | g0032 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02976 | hp2 | a0002 | c0004 | t0005 | g0342 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03041 | hp1 | a0005 | c0008 | t0007 | g0004 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03041 | hp2 | a0003 | c0005 | t0004 | g0313 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03098 | hp1 | a0001 | c0003 | t0003 | g0325 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03098 | hp2 | a0002 | c0004 | t0001 | g0337 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03139 | hp1 | a0015 | c0025 | t0010 | g0350 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03139 | hp2 | a0001 | c0003 | t0003 | g0026 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03195 | hp1 | a0001 | c0001 | t0024 | g0331 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03209 | hp1 | a0005 | c0008 | t0007 | g0352 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03209 | hp2 | a0002 | c0004 | t0005 | g0335 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03225 | hp1 | a0008 | c0012 | t0010 | g0309 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03453 | hp1 | a0001 | c0023 | t0015 | g0316 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03453 | hp2 | a0003 | c0027 | t0031 | g0100 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0305 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03490 | hp2 | a0001 | c0001 | t0012 | g0288 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03491 | hp2 | a0001 | c0007 | t0008 | g0006 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03492 | hp2 | a0001 | c0007 | t0008 | g0006 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03516 | hp1 | a0002 | c0004 | t0005 | g0341 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03516 | hp2 | a0003 | c0005 | t0004 | g0312 | AFR | ESN | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03540 | hp1 | a0008 | c0012 | t0010 | g0311 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03540 | hp2 | a0002 | c0004 | t0001 | g0339 | AFR | GWD | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03579 | hp1 | a0005 | c0008 | t0007 | g0004 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03579 | hp2 | a0003 | c0005 | t0004 | g0318 | AFR | MSL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0059 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0102 | SAS | PJL | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0092 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03831 | hp2 | a0016 | c0018 | t0001 | g0133 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03927 | hp1 | a0001 | c0014 | t0016 | g0110 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04184 | hp1 | a0001 | c0001 | t0027 | g0190 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0073 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18522 | hp1 | a0005 | c0008 | t0007 | g0353 | AFR | YRI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18522 | hp2 | a0001 | c0001 | t0025 | g0165 | AFR | YRI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18906 | hp1 | a0002 | c0004 | t0001 | g0338 | AFR | YRI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18906 | hp2 | a0001 | c0009 | t0005 | g0009 | AFR | YRI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18948 | hp2 | a0001 | c0002 | t0006 | g0087 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18954 | hp2 | a0017 | c0016 | t0001 | g0192 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18962 | hp1 | a0001 | c0001 | t0030 | g0224 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18966 | hp1 | a0001 | c0002 | t0006 | g0066 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18969 | hp2 | a0004 | c0006 | t0001 | g0209 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18975 | hp2 | a0004 | c0006 | t0001 | g0208 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18983 | hp1 | a0004 | c0006 | t0001 | g0017 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18990 | hp1 | a0001 | c0002 | t0020 | g0064 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18994 | hp2 | a0007 | c0011 | t0009 | g0245 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19002 | hp2 | a0007 | c0011 | t0009 | g0246 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19006 | hp2 | a0001 | c0002 | t0006 | g0063 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19030 | hp1 | a0002 | c0004 | t0004 | g0028 | AFR | LWK | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19030 | hp2 | a0001 | c0003 | t0029 | g0326 | AFR | LWK | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | LWK | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | LWK | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19055 | hp1 | a0004 | c0006 | t0001 | g0017 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19057 | hp2 | a0018 | c0019 | t0001 | g0226 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19060 | hp2 | a0004 | c0006 | t0001 | g0206 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19065 | hp1 | a0001 | c0002 | t0006 | g0068 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19065 | hp2 | a0001 | c0002 | t0021 | g0069 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19080 | hp2 | a0004 | c0006 | t0001 | g0204 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19083 | hp1 | a0007 | c0011 | t0009 | g0293 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19240 | hp1 | a0002 | c0004 | t0004 | g0028 | AFR | YRI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA19240 | hp2 | a0006 | c0010 | t0033 | g0037 | AFR | YRI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20129 | hp1 | a0002 | c0004 | t0005 | g0349 | AFR | ASW | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20129 | hp2 | a0006 | c0010 | t0014 | g0034 | AFR | ASW | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20805 | hp1 | a0001 | c0002 | t0006 | g0103 | EUR | TSI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | GIH | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20905 | hp2 | a0001 | c0013 | t0015 | g0186 | SAS | GIH | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01123 | hp1 | a0001 | c0009 | t0001 | g0108 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0042 | AMR | CLM | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02109 | hp1 | a0001 | c0007 | t0008 | g0030 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02109 | hp2 | a0001 | c0002 | t0022 | g0101 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02486 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02486 | hp2 | a0001 | c0003 | t0003 | g0329 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02559 | hp1 | a0014 | c0024 | t0005 | g0348 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | USA | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
HG06807 | hp2 | a0006 | c0010 | t0014 | g0035 | AFR | USA | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20300 | hp1 | a0001 | c0003 | t0003 | g0322 | AFR | USA | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA20300 | hp2 | a0001 | c0009 | t0005 | g0009 | AFR | USA | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
NA21309 | hp2 | a0006 | c0010 | t0017 | g0031 | AFR | LWK | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0270 | REF | REF | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
homoSapiens | grch38p0 | a0002 | c0004 | t0001 | g0003 | REF | REF | CFAP91_chr3_119698022_119772102 | CFAP91 | chr3 | 119698022 | 119772102 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119703190 | TCTC | T | 1 | a0007 | 4 | HG00597.hp1 NA18994.hp2 NA19002.hp2 others(1): Show |
conservative_inframe_deletion | MODERATE | c.97_99delTCC | p.Ser33del | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/18 | 174/4433 | 97/2304 | 33/767 | INFO_REALIGN_3_PRIME | chr3 | 119703190 | ||
chr3:119707464 | C | G | 1 | a0004 | 7 | HG00423.hp2 NA18969.hp2 NA18975.hp2 others(4): Show |
missense_variant | MODERATE | c.262C>G | p.Leu88Val | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/18 | 339/4433 | 262/2304 | 88/767 | chr3 | 119707464 | |||
chr3:119707552 | A | C | 1 | a0018 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.350A>C | p.Gln117Pro | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/18 | 427/4433 | 350/2304 | 117/767 | chr3 | 119707552 | |||
chr3:119708634 | C | T | 1 | a0016 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.403C>T | p.Pro135Ser | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/18 | 480/4433 | 403/2304 | 135/767 | chr3 | 119708634 | |||
chr3:119715680 | G | C | 14 | a0001 a0003 a0004 others(11): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
missense_variant | MODERATE | c.619G>C | p.Ala207Pro | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/18 | 696/4433 | 619/2304 | 207/767 | chr3 | 119715680 | |||
chr3:119715707 | A | G | 1 | a0015 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.646A>G | p.Ile216Val | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/18 | 723/4433 | 646/2304 | 216/767 | chr3 | 119715707 | |||
chr3:119726245 | T | A | 3 | a0005 a0010 a0013 |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
missense_variant | MODERATE | c.757T>A | p.Ser253Thr | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/18 | 834/4433 | 757/2304 | 253/767 | chr3 | 119726245 | |||
chr3:119730312 | G | A | 1 | a0009 | 2 | HG01109.hp2 HG01433.hp2 |
missense_variant | MODERATE | c.953G>A | p.Arg318Gln | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/18 | 1030/4433 | 953/2304 | 318/767 | chr3 | 119730312 | |||
chr3:119730318 | C | G | 2 | a0005 a0010 |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.959C>G | p.Ser320Cys | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/18 | 1036/4433 | 959/2304 | 320/767 | chr3 | 119730318 | |||
chr3:119730366 | C | T | 1 | a0011 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1007C>T | p.Thr336Met | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/18 | 1084/4433 | 1007/2304 | 336/767 | chr3 | 119730366 | |||
chr3:119732405 | G | A | 1 | a0006 | 5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
missense_variant | MODERATE | c.1130G>A | p.Arg377His | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 9/18 | 1207/4433 | 1130/2304 | 377/767 | chr3 | 119732405 | |||
chr3:119737415 | G | A | 1 | a0003 | 12 | HG01099.hp2 HG01106.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.1394G>A | p.Arg465His | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/18 | 1471/4433 | 1394/2304 | 465/767 | chr3 | 119737415 | |||
chr3:119747178 | G | A | 3 | a0005 a0010 a0013 |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
missense_variant | MODERATE | c.1966G>A | p.Ala656Thr | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 15/18 | 2043/4433 | 1966/2304 | 656/767 | chr3 | 119747178 | |||
chr3:119747851 | G | A | 1 | a0017 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.2092G>A | p.Val698Ile | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/18 | 2169/4433 | 2092/2304 | 698/767 | chr3 | 119747851 | |||
chr3:119750942 | A | T | 1 | a0014 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.2149A>T | p.Asn717Tyr | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/18 | 2226/4433 | 2149/2304 | 717/767 | chr3 | 119750942 | |||
chr3:119750994 | C | T | 2 | a0008 a0015 |
4 | HG02622.hp1 HG03139.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.2201C>T | p.Thr734Met | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/18 | 2278/4433 | 2201/2304 | 734/767 | chr3 | 119750994 | |||
chr3:119751036 | A | G | 1 | a0012 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2243A>G | p.Asp748Gly | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/18 | 2320/4433 | 2243/2304 | 748/767 | chr3 | 119751036 | |||
chr3:119767102 | A | T | 9 | a0001 a0002 a0003 others(6): Show |
144 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(141): Show |
splice_region_variant | LOW | c.*2052A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | chr3 | 119767102 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119703116 | C | T | 6 | a0001c0002 a0001c0007 a0003c0027 others(3): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
synonymous_variant | LOW | c.18C>T | p.Thr6Thr | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/18 | 95/4433 | 18/2304 | 6/767 | chr3 | 119703116 | |||
chr3:119707460 | T | C | 9 | a0001c0001 a0001c0013 a0004c0006 others(6): Show |
224 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
synonymous_variant | LOW | c.258T>C | p.Tyr86Tyr | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/18 | 335/4433 | 258/2304 | 86/767 | chr3 | 119707460 | |||
chr3:119709887 | C | T | 2 | a0001c0009 a0001c0014 |
7 | HG01123.hp1 HG02280.hp1 HG02698.hp2 others(4): Show |
synonymous_variant | LOW | c.492C>T | p.Ala164Ala | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/18 | 569/4433 | 492/2304 | 164/767 | chr3 | 119709887 | |||
chr3:119726292 | A | G | 4 | a0005c0008 a0010c0015 a0010c0021 others(1): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
synonymous_variant | LOW | c.804A>G | p.Lys268Lys | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/18 | 881/4433 | 804/2304 | 268/767 | chr3 | 119726292 | |||
chr3:119726334 | G | A | 1 | a0001c0014 | 2 | HG02698.hp2 HG03927.hp1 |
synonymous_variant | LOW | c.846G>A | p.Glu282Glu | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/18 | 923/4433 | 846/2304 | 282/767 | chr3 | 119726334 | |||
chr3:119744112 | G | A | 1 | a0009c0022 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1818G>A | p.Gln606Gln | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/18 | 1895/4433 | 1818/2304 | 606/767 | chr3 | 119744112 | |||
chr3:119747180 | G | A | 3 | a0001c0007 a0001c0013 a0001c0023 |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
synonymous_variant | LOW | c.1968G>A | p.Ala656Ala | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 15/18 | 2045/4433 | 1968/2304 | 656/767 | chr3 | 119747180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119703061 | C | G | 1 | a0001c0003t0018 | 2 | HG02055.hp2 HG02572.hp2 |
5_prime_UTR_variant | MODIFIER | c.-38C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/18 | 38 | chr3 | 119703061 | ||||||
chr3:119703064 | T | A | 9 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0013 others(6): Show |
73 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
5_prime_UTR_variant | MODIFIER | c.-35T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/18 | 35 | chr3 | 119703064 | ||||||
chr3:119703087 | A | G | 14 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0013 others(11): Show |
85 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-12A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/18 | 12 | chr3 | 119703087 | ||||||
chr3:119765160 | A | T | 1 | a0006c0010t0033 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 14063 | chr3 | 119765160 | ||||||
chr3:119765194 | A | G | 1 | a0001c0014t0016 | 2 | HG02698.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*144A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 14097 | chr3 | 119765194 | ||||||
chr3:119765204 | A | G | 1 | a0001c0001t0030 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 14107 | chr3 | 119765204 | ||||||
chr3:119765280 | A | G | 1 | a0001c0003t0029 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 14183 | chr3 | 119765280 | ||||||
chr3:119765731 | A | T | 4 | a0001c0007t0008 a0001c0013t0015 a0001c0013t0028 others(1): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*681A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 14634 | chr3 | 119765731 | ||||||
chr3:119765754 | T | G | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0002t0002 others(10): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*704T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 14657 | chr3 | 119765754 | ||||||
chr3:119765820 | T | C | 1 | a0001c0002t0019 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*770T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 14723 | chr3 | 119765820 | ||||||
chr3:119766147 | G | A | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0024 others(10): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1097G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15050 | chr3 | 119766147 | ||||||
chr3:119766153 | CATTT | C | 1 | a0001c0001t0011 | 3 | HG01069.hp1 HG01106.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1107_*1110delTATT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15060 | INFO_REALIGN_3_PRIME | chr3 | 119766153 | |||||
chr3:119766234 | T | TCCCACAG | 5 | a0001c0001t0004 a0001c0003t0004 a0002c0004t0004 others(2): Show |
18 | HG01099.hp2 HG01106.hp2 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1186_*1192dupCCAC others(3): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15146 | INFO_REALIGN_3_PRIME | chr3 | 119766234 | |||||
chr3:119766243 | A | G | 5 | a0001c0001t0004 a0001c0003t0004 a0002c0004t0004 others(2): Show |
18 | HG01099.hp2 HG01106.hp2 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1193A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15146 | chr3 | 119766243 | ||||||
chr3:119766268 | A | G | 1 | a0001c0003t0018 | 2 | HG02055.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1218A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15171 | chr3 | 119766268 | ||||||
chr3:119766329 | A | T | 10 | a0001c0001t0012 a0001c0002t0021 a0001c0002t0022 others(7): Show |
19 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1279A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15232 | chr3 | 119766329 | ||||||
chr3:119766349 | C | G | 1 | a0001c0001t0027 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1299C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15252 | chr3 | 119766349 | ||||||
chr3:119766370 | C | G | 1 | a0001c0002t0020 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1320C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15273 | chr3 | 119766370 | ||||||
chr3:119766521 | A | C | 2 | a0001c0014t0016 a0013c0020t0026 |
3 | HG02145.hp1 HG02698.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1471A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15424 | chr3 | 119766521 | ||||||
chr3:119766717 | T | A | 2 | a0001c0002t0013 a0001c0002t0022 |
3 | HG00735.hp2 HG02109.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1667T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15620 | chr3 | 119766717 | ||||||
chr3:119766718 | C | A | 2 | a0001c0002t0013 a0001c0002t0022 |
3 | HG00735.hp2 HG02109.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1668C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15621 | chr3 | 119766718 | ||||||
chr3:119766739 | A | G | 35 | a0001c0001t0003 a0001c0001t0004 a0001c0002t0002 others(32): Show |
152 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1689A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15642 | chr3 | 119766739 | ||||||
chr3:119766925 | C | G | 1 | a0001c0001t0025 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1875C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15828 | chr3 | 119766925 | ||||||
chr3:119766944 | C | T | 1 | a0007c0011t0009 | 4 | HG00597.hp1 NA18994.hp2 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1894C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15847 | chr3 | 119766944 | ||||||
chr3:119767060 | T | C | 3 | a0005c0008t0007 a0010c0015t0007 a0010c0021t0007 |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2010T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 18/18 | 15963 | chr3 | 119767060 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119703259 | C | A | 79 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(76): Show |
85 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.124+37C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703259 | |||||||
chr3:119703357 | T | C | 330 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.124+135T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703357 | |||||||
chr3:119703454 | C | T | 1 | a0003c0005t0004g0334 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.124+232C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703454 | |||||||
chr3:119703465 | T | C | 330 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.124+243T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703465 | |||||||
chr3:119703569 | G | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.124+347G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703569 | |||||||
chr3:119703620 | G | GC | 3 | a0001c0002t0002g0008 a0001c0002t0002g0102 a0001c0002t0006g0103 |
4 | HG01069.hp2 HG01071.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+400dupC | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 119703620 | ||||||
chr3:119703653 | T | C | 2 | a0002c0004t0005g0335 a0002c0004t0005g0336 |
2 | HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.124+431T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703653 | |||||||
chr3:119703654 | G | T | 6 | a0001c0014t0016g0109 a0001c0014t0016g0110 a0005c0008t0007g0004 others(3): Show |
8 | HG02615.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+432G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703654 | |||||||
chr3:119703729 | G | C | 80 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.124+507G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703729 | |||||||
chr3:119703890 | T | G | 10 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(7): Show |
12 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.124+668T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119703890 | |||||||
chr3:119703942 | A | AT | 87 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(84): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+726dupT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 119703942 | ||||||
chr3:119704011 | G | A | 1 | a0001c0009t0005g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124+789G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704011 | |||||||
chr3:119704185 | T | C | 80 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.124+963T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704185 | |||||||
chr3:119704190 | G | A | 1 | a0001c0002t0002g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.124+968G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704190 | |||||||
chr3:119704238 | C | T | 1 | a0015c0025t0010g0350 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.124+1016C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704238 | |||||||
chr3:119704301 | C | T | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.124+1079C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704301 | |||||||
chr3:119704727 | C | T | 1 | a0002c0004t0005g0349 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.124+1505C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704727 | |||||||
chr3:119704740 | A | T | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124+1518A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704740 | |||||||
chr3:119704762 | C | T | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124+1540C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704762 | |||||||
chr3:119704790 | C | A | 1 | a0003c0005t0004g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.124+1568C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704790 | |||||||
chr3:119704809 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.124+1587G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704809 | |||||||
chr3:119704884 | T | C | 1 | a0001c0001t0003g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.124+1662T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119704884 | |||||||
chr3:119705290 | G | T | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.125-1519G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119705290 | |||||||
chr3:119705359 | T | C | 334 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.125-1450T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119705359 | |||||||
chr3:119705468 | C | T | 1 | a0001c0001t0024g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.125-1341C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119705468 | |||||||
chr3:119705766 | G | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(205): Show |
224 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.125-1043G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119705766 | |||||||
chr3:119705871 | G | T | 10 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(7): Show |
12 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.125-938G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119705871 | |||||||
chr3:119705874 | G | A | 3 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0004g0303 |
3 | HG01884.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.125-935G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119705874 | |||||||
chr3:119705975 | C | A | 67 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(64): Show |
71 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.125-834C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119705975 | |||||||
chr3:119706013 | A | G | 4 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0014t0016g0109 others(1): Show |
4 | HG01123.hp1 HG02698.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-796A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706013 | |||||||
chr3:119706153 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.125-656G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706153 | |||||||
chr3:119706265 | C | G | 1 | a0001c0002t0002g0098 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.125-544C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706265 | |||||||
chr3:119706307 | G | A | 1 | a0001c0001t0024g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.125-502G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706307 | |||||||
chr3:119706330 | G | A | 10 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(7): Show |
12 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.125-479G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706330 | |||||||
chr3:119706502 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.125-307A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706502 | |||||||
chr3:119706575 | C | T | 6 | a0001c0001t0001g0299 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01069.hp1 HG01099.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-234C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706575 | |||||||
chr3:119706610 | A | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.125-199A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706610 | |||||||
chr3:119706613 | T | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.125-196T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706613 | |||||||
chr3:119706638 | G | T | 1 | a0001c0001t0001g0296 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.125-171G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706638 | |||||||
chr3:119706790 | T | G | 2 | a0003c0005t0004g0306 a0003c0005t0004g0307 |
2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.125-19T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 1/17 | chr3 | 119706790 | |||||||
chr3:119707190 | T | C | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.202-214T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 2/17 | chr3 | 119707190 | |||||||
chr3:119707208 | C | G | 80 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.202-196C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 2/17 | chr3 | 119707208 | |||||||
chr3:119707732 | G | GAT | 4 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG02135.hp1 NA18974.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.359+187_359+188dup others(2): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(1): Show |
4 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0014t0016g0109 others(1): Show |
4 | HG01123.hp1 HG02145.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+181_359+188dup others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(3): Show |
2 | a0001c0009t0005g0105 a0001c0014t0016g0110 |
2 | HG02280.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.359+179_359+188dup others(10): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(5): Show |
2 | a0001c0002t0013g0104 a0001c0009t0005g0009 |
3 | HG00735.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.359+177_359+188dup others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(7): Show |
3 | a0001c0002t0022g0101 a0001c0007t0008g0030 a0006c0010t0017g0031 |
3 | HG02109.hp1 HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.359+175_359+188dup others(14): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(9): Show |
16 | a0001c0002t0002g0001 a0001c0002t0002g0040 a0001c0002t0002g0041 others(13): Show |
19 | HG00639.hp2 HG01081.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.359+173_359+188dup others(16): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(11): Show |
22 | a0001c0002t0002g0008 a0001c0002t0002g0038 a0001c0002t0002g0049 others(19): Show |
23 | HG00099.hp2 HG00408.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.359+188_359+189ins others(18): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(13): Show |
19 | a0001c0002t0002g0007 a0001c0002t0002g0067 a0001c0002t0002g0071 others(16): Show |
21 | HG02015.hp1 HG02083.hp2 HG02683.hp2 others(18): Show |
intron_variant | MODIFIER | c.359+188_359+189ins others(20): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(15): Show |
10 | a0001c0002t0002g0082 a0001c0002t0002g0084 a0001c0002t0002g0085 others(7): Show |
10 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.359+188_359+189ins others(22): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(17): Show |
4 | a0001c0002t0002g0092 a0001c0002t0002g0093 a0001c0002t0002g0094 others(1): Show |
4 | HG00609.hp1 HG03831.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.359+188_359+189ins others(24): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(19): Show |
1 | a0001c0002t0002g0096 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.359+188_359+189ins others(26): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(21): Show |
1 | a0009c0026t0032g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.359+188_359+189ins others(28): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707732 | G | GATATATA others(25): Show |
2 | a0001c0002t0002g0097 a0003c0027t0031g0100 |
2 | HG03453.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.359+188_359+189ins others(32): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119707732 | ||||||
chr3:119707808 | G | A | 6 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0009t0005g0009 others(3): Show |
7 | HG01123.hp1 HG02280.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.359+247G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119707808 | |||||||
chr3:119707831 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.359+270C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119707831 | |||||||
chr3:119707863 | T | C | 4 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0014t0016g0109 others(1): Show |
4 | HG01123.hp1 HG02698.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.359+302T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119707863 | |||||||
chr3:119708001 | G | T | 1 | a0006c0010t0017g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.359+440G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119708001 | |||||||
chr3:119708118 | A | G | 1 | a0014c0024t0005g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.360-473A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119708118 | |||||||
chr3:119708149 | C | A | 4 | a0008c0012t0010g0309 a0008c0012t0010g0310 a0008c0012t0010g0311 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.360-442C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119708149 | |||||||
chr3:119708251 | C | T | 1 | a0003c0027t0031g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.360-340C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119708251 | |||||||
chr3:119708264 | CA | C | 246 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(243): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.360-307delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119708264 | ||||||
chr3:119708264 | CAA | C | 21 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0289 others(18): Show |
24 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.360-308_360-307del others(2): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 119708264 | ||||||
chr3:119708341 | G | T | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-250G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119708341 | |||||||
chr3:119708360 | T | C | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.360-231T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119708360 | |||||||
chr3:119708370 | T | G | 2 | a0001c0009t0001g0107 a0001c0009t0001g0108 |
2 | HG01123.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.360-221T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 3/17 | chr3 | 119708370 | |||||||
chr3:119708826 | G | A | 334 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.443+152G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119708826 | |||||||
chr3:119708885 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.443+211G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119708885 | |||||||
chr3:119708917 | C | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.443+243C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119708917 | |||||||
chr3:119709034 | C | T | 12 | a0001c0023t0015g0316 a0003c0005t0004g0111 a0003c0005t0004g0306 others(9): Show |
12 | HG01099.hp2 HG01106.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.443+360C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709034 | |||||||
chr3:119709128 | A | T | 87 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(84): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.443+454A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709128 | |||||||
chr3:119709142 | A | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.443+468A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709142 | |||||||
chr3:119709244 | A | G | 1 | a0001c0001t0003g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.443+570A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709244 | |||||||
chr3:119709485 | T | C | 1 | a0002c0004t0001g0337 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.444-354T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709485 | |||||||
chr3:119709578 | T | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.444-261T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709578 | |||||||
chr3:119709629 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.444-210A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709629 | |||||||
chr3:119709682 | C | A | 65 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(62): Show |
69 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.444-157C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709682 | |||||||
chr3:119709811 | C | G | 1 | a0001c0001t0001g0284 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.444-28C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 4/17 | chr3 | 119709811 | |||||||
chr3:119710122 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.500+227A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119710122 | |||||||
chr3:119710145 | T | C | 4 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(1): Show |
6 | HG02615.hp1 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+250T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119710145 | |||||||
chr3:119710148 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.500+253G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119710148 | |||||||
chr3:119710511 | C | T | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.500+616C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119710511 | |||||||
chr3:119710523 | C | T | 7 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0005c0008t0007g0004 others(4): Show |
10 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+628C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119710523 | |||||||
chr3:119710548 | T | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | NA19002.hp1 NA19055.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.500+653T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119710548 | |||||||
chr3:119710962 | A | C | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.500+1067A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119710962 | |||||||
chr3:119711150 | G | A | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.500+1255G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711150 | |||||||
chr3:119711357 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.500+1462A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711357 | |||||||
chr3:119711378 | A | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.500+1483A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711378 | |||||||
chr3:119711442 | C | T | 33 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0328 others(30): Show |
36 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.500+1547C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711442 | |||||||
chr3:119711458 | G | A | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.500+1563G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711458 | |||||||
chr3:119711618 | T | C | 7 | a0001c0003t0001g0330 a0001c0003t0003g0025 a0001c0003t0003g0027 others(4): Show |
9 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+1723T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711618 | |||||||
chr3:119711631 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02523.hp1 NA18986.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.500+1736A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711631 | |||||||
chr3:119711684 | C | T | 33 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0328 others(30): Show |
36 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.500+1789C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119711684 | |||||||
chr3:119712035 | A | G | 1 | a0003c0005t0004g0319 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.500+2140A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712035 | |||||||
chr3:119712111 | C | A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.500+2216C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712111 | |||||||
chr3:119712137 | G | A | 6 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0009t0005g0009 others(3): Show |
7 | HG01123.hp1 HG02280.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.500+2242G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712137 | |||||||
chr3:119712174 | C | T | 4 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0014t0016g0109 others(1): Show |
4 | HG01123.hp1 HG02698.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+2279C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712174 | |||||||
chr3:119712547 | A | G | 2 | a0001c0002t0002g0038 a0001c0002t0020g0064 |
2 | HG00408.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.500+2652A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712547 | |||||||
chr3:119712650 | A | G | 9 | a0001c0001t0001g0158 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG01358.hp1 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+2755A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712650 | |||||||
chr3:119712745 | A | G | 5 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0096 others(2): Show |
5 | NA18983.hp2 NA18990.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-2817A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712745 | |||||||
chr3:119712797 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.501-2765A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712797 | |||||||
chr3:119712821 | G | C | 4 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0032 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-2741G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712821 | |||||||
chr3:119712971 | C | CA | 17 | a0001c0001t0003g0116 a0001c0003t0001g0304 a0001c0003t0001g0305 others(14): Show |
17 | HG01099.hp2 HG01106.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.501-2579dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119712971 | ||||||
chr3:119712971 | CA | C | 65 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(62): Show |
69 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.501-2579delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119712971 | ||||||
chr3:119712982 | A | C | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0265 others(4): Show |
7 | HG01255.hp1 HG01496.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-2580A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712982 | |||||||
chr3:119712983 | A | C | 1 | a0001c0001t0001g0264 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.501-2579A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712983 | |||||||
chr3:119712983 | AC | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG02647.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-2578delC | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119712983 | |||||||
chr3:119713064 | T | A | 33 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0328 others(30): Show |
36 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.501-2498T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713064 | |||||||
chr3:119713083 | T | TTTTA | 7 | a0001c0002t0002g0082 a0001c0002t0006g0068 a0001c0002t0021g0069 others(4): Show |
9 | HG02615.hp1 HG03041.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-2431_501-2428d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119713083 | ||||||
chr3:119713083 | TTTTA | T | 41 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(38): Show |
43 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.501-2431_501-2428d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119713083 | ||||||
chr3:119713083 | TTTTATTT others(1): Show |
T | 58 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0125 others(55): Show |
64 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.501-2435_501-2428d others(10): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119713083 | ||||||
chr3:119713083 | TTTTATTT others(5): Show |
T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
211 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.501-2439_501-2428d others(14): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119713083 | ||||||
chr3:119713083 | TTTTATTT others(9): Show |
T | 3 | a0001c0001t0001g0302 a0001c0003t0018g0332 a0001c0003t0018g0333 |
3 | HG01361.hp1 HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.501-2443_501-2428d others(18): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119713083 | ||||||
chr3:119713188 | C | T | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.501-2374C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713188 | |||||||
chr3:119713194 | G | A | 65 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(62): Show |
69 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.501-2368G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713194 | |||||||
chr3:119713384 | C | G | 2 | a0003c0027t0031g0100 a0009c0026t0032g0099 |
2 | HG01433.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.501-2178C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713384 | |||||||
chr3:119713398 | A | G | 1 | a0001c0003t0003g0025 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.501-2164A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713398 | |||||||
chr3:119713416 | C | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.501-2146C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713416 | |||||||
chr3:119713418 | CT | C | 80 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.501-2130delT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119713418 | ||||||
chr3:119713561 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.501-2001T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713561 | |||||||
chr3:119713806 | C | A | 1 | a0001c0001t0003g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.501-1756C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713806 | |||||||
chr3:119713939 | A | C | 1 | a0001c0002t0002g0095 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.501-1623A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713939 | |||||||
chr3:119713945 | G | C | 1 | a0001c0002t0002g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.501-1617G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119713945 | |||||||
chr3:119714114 | G | A | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.501-1448G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714114 | |||||||
chr3:119714206 | C | CA | 7 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0172 others(4): Show |
8 | HG02280.hp1 NA18906.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-1346dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119714206 | ||||||
chr3:119714221 | C | A | 3 | a0008c0012t0010g0309 a0008c0012t0010g0311 a0010c0021t0007g0308 |
3 | HG02965.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.501-1341C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714221 | |||||||
chr3:119714258 | C | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.501-1304C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714258 | |||||||
chr3:119714272 | A | T | 4 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0014t0016g0109 others(1): Show |
4 | HG01123.hp1 HG02698.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-1290A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714272 | |||||||
chr3:119714353 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0175 |
3 | HG02257.hp2 HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.501-1209G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714353 | |||||||
chr3:119714357 | C | T | 1 | a0001c0002t0002g0056 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.501-1205C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714357 | |||||||
chr3:119714365 | C | CA | 7 | a0001c0002t0002g0049 a0001c0002t0002g0060 a0001c0002t0002g0102 others(4): Show |
8 | HG01978.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-1177dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119714365 | ||||||
chr3:119714365 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0002g0047 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.501-1187_501-1177d others(13): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119714365 | ||||||
chr3:119714382 | A | AAG | 29 | a0001c0001t0001g0016 a0001c0001t0001g0130 a0001c0001t0001g0176 others(26): Show |
30 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.501-1179_501-1178i others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 119714382 | ||||||
chr3:119714382 | A | AG | 211 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(208): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.501-1180_501-1179i others(3): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714382 | |||||||
chr3:119714382 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0263 |
2 | HG03195.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.501-1180A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714382 | |||||||
chr3:119714407 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.501-1155C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714407 | |||||||
chr3:119714453 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.501-1109A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714453 | |||||||
chr3:119714498 | G | C | 6 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0009t0005g0009 others(3): Show |
7 | HG01123.hp1 HG02280.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-1064G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714498 | |||||||
chr3:119714557 | G | A | 80 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.501-1005G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714557 | |||||||
chr3:119714661 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
65 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.501-901A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714661 | |||||||
chr3:119714726 | T | C | 79 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(76): Show |
85 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.501-836T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714726 | |||||||
chr3:119714726 | T | G | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.501-836T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119714726 | |||||||
chr3:119715002 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.501-560T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119715002 | |||||||
chr3:119715017 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.501-545A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119715017 | |||||||
chr3:119715158 | C | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.501-404C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 5/17 | chr3 | 119715158 | |||||||
chr3:119715838 | A | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.682+95A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119715838 | |||||||
chr3:119715892 | C | T | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.682+149C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119715892 | |||||||
chr3:119716290 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.682+547C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716290 | |||||||
chr3:119716389 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.682+646G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716389 | |||||||
chr3:119716466 | G | C | 330 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.682+723G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716466 | |||||||
chr3:119716487 | A | G | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.682+744A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716487 | |||||||
chr3:119716717 | G | C | 80 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.682+974G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716717 | |||||||
chr3:119716792 | G | A | 13 | a0001c0003t0001g0328 a0001c0003t0001g0330 a0001c0003t0003g0025 others(10): Show |
16 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.682+1049G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716792 | |||||||
chr3:119716867 | G | A | 4 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0004g0303 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1124G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716867 | |||||||
chr3:119716936 | G | A | 33 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0328 others(30): Show |
36 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.682+1193G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119716936 | |||||||
chr3:119717045 | C | T | 1 | a0001c0003t0003g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.682+1302C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717045 | |||||||
chr3:119717046 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | NA18986.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.682+1303G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717046 | |||||||
chr3:119717054 | G | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG01978.hp1 HG01981.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+1311G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717054 | |||||||
chr3:119717064 | C | A | 2 | a0001c0009t0001g0107 a0001c0009t0001g0108 |
2 | HG01123.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.682+1321C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717064 | |||||||
chr3:119717162 | G | T | 67 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(64): Show |
71 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.682+1419G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717162 | |||||||
chr3:119717351 | A | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.682+1608A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717351 | |||||||
chr3:119717380 | G | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.682+1637G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717380 | |||||||
chr3:119717548 | T | TG | 179 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
191 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.682+1807dupG | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119717548 | ||||||
chr3:119717550 | G | GGT | 32 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0158 others(29): Show |
34 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.682+1807_682+1808i others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717550 | |||||||
chr3:119717550 | GT | G | 84 | a0001c0001t0001g0010 a0001c0002t0002g0001 a0001c0002t0002g0007 others(81): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.682+1826delT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119717550 | ||||||
chr3:119717551 | T | G | 33 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0125 others(30): Show |
37 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.682+1808T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717551 | |||||||
chr3:119717552 | T | G | 77 | a0001c0001t0001g0010 a0001c0002t0002g0001 a0001c0002t0002g0007 others(74): Show |
84 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.682+1809T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717552 | |||||||
chr3:119717553 | T | G | 3 | a0001c0009t0005g0009 a0001c0009t0005g0105 a0009c0026t0032g0099 |
4 | HG01433.hp2 HG02280.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+1810T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717553 | |||||||
chr3:119717554 | T | G | 5 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0014t0016g0109 others(2): Show |
5 | HG01123.hp1 HG02145.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+1811T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717554 | |||||||
chr3:119717569 | T | C | 2 | a0001c0002t0022g0101 a0013c0020t0026g0106 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.682+1826T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717569 | |||||||
chr3:119717912 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.682+2169A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717912 | |||||||
chr3:119717990 | G | C | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.682+2247G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717990 | |||||||
chr3:119717998 | G | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): Show |
109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.682+2255G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119717998 | |||||||
chr3:119718057 | T | C | 1 | a0016c0018t0001g0133 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.682+2314T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718057 | |||||||
chr3:119718066 | C | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0176 a0001c0001t0001g0193 others(4): Show |
7 | HG02074.hp2 HG02135.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+2323C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718066 | |||||||
chr3:119718080 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.682+2337C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718080 | |||||||
chr3:119718092 | C | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.682+2349C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718092 | |||||||
chr3:119718155 | A | G | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.682+2412A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718155 | |||||||
chr3:119718251 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.682+2508A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718251 | |||||||
chr3:119718269 | A | G | 80 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.682+2526A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718269 | |||||||
chr3:119718284 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(124): Show |
138 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.682+2541T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718284 | |||||||
chr3:119718439 | T | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.682+2696T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718439 | |||||||
chr3:119718501 | A | T | 1 | a0001c0002t0002g0055 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.682+2758A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718501 | |||||||
chr3:119718725 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.682+2982A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718725 | |||||||
chr3:119718783 | C | T | 6 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0009t0005g0009 others(3): Show |
7 | HG01123.hp1 HG02280.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+3040C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718783 | |||||||
chr3:119718868 | T | C | 4 | a0008c0012t0010g0309 a0008c0012t0010g0310 a0008c0012t0010g0311 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+3125T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718868 | |||||||
chr3:119718909 | C | CA | 25 | a0001c0001t0001g0024 a0001c0001t0001g0158 a0001c0001t0001g0240 others(22): Show |
30 | HG01123.hp1 HG01433.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.682+3180dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119718909 | ||||||
chr3:119718909 | CA | C | 38 | a0001c0002t0002g0047 a0001c0002t0002g0073 a0001c0002t0022g0101 others(35): Show |
43 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+3180delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119718909 | ||||||
chr3:119718995 | C | T | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.682+3252C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119718995 | |||||||
chr3:119719102 | A | G | 4 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0014t0016g0109 others(1): Show |
4 | HG01123.hp1 HG02698.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+3359A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719102 | |||||||
chr3:119719151 | G | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0128 a0001c0001t0001g0151 others(3): Show |
7 | HG00558.hp1 HG02056.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+3408G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719151 | |||||||
chr3:119719160 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.682+3417T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719160 | |||||||
chr3:119719216 | A | G | 1 | a0001c0002t0002g0095 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.682+3473A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719216 | |||||||
chr3:119719238 | G | A | 330 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.682+3495G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719238 | |||||||
chr3:119719288 | A | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.682+3545A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719288 | |||||||
chr3:119719341 | T | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.682+3598T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719341 | |||||||
chr3:119719408 | A | T | 79 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0008 others(76): Show |
85 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.682+3665A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719408 | |||||||
chr3:119719443 | G | T | 11 | a0002c0004t0005g0335 a0002c0004t0005g0336 a0002c0004t0005g0340 others(8): Show |
11 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.682+3700G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719443 | |||||||
chr3:119719761 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.682+4018A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719761 | |||||||
chr3:119719763 | C | T | 6 | a0001c0009t0001g0107 a0001c0009t0001g0108 a0001c0009t0005g0009 others(3): Show |
7 | HG01123.hp1 HG02280.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+4020C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719763 | |||||||
chr3:119719931 | C | T | 1 | a0001c0001t0024g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.682+4188C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719931 | |||||||
chr3:119719985 | C | T | 1 | a0001c0001t0024g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.682+4242C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119719985 | |||||||
chr3:119720070 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.682+4327G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720070 | |||||||
chr3:119720087 | C | CA | 8 | a0001c0003t0003g0025 a0001c0003t0003g0320 a0001c0003t0003g0321 others(5): Show |
11 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+4357dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119720087 | ||||||
chr3:119720145 | T | C | 1 | a0003c0005t0004g0306 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.682+4402T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720145 | |||||||
chr3:119720204 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.682+4461T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720204 | |||||||
chr3:119720232 | C | CA | 74 | a0001c0001t0001g0162 a0001c0001t0001g0198 a0001c0001t0001g0258 others(71): Show |
79 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.682+4504dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119720232 | ||||||
chr3:119720232 | C | CAA | 13 | a0001c0002t0002g0050 a0001c0002t0002g0059 a0001c0007t0008g0005 others(10): Show |
15 | HG01891.hp1 HG01891.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.682+4503_682+4504d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119720232 | ||||||
chr3:119720258 | G | C | 334 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.682+4515G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720258 | |||||||
chr3:119720259 | C | T | 334 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.682+4516C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720259 | |||||||
chr3:119720322 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
5 | NA18946.hp2 NA18957.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+4579G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720322 | |||||||
chr3:119720324 | G | A | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.682+4581G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720324 | |||||||
chr3:119720396 | C | CA | 211 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(208): Show |
228 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.682+4666dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119720396 | ||||||
chr3:119720405 | AAAAAG | A | 7 | a0001c0002t0013g0104 a0001c0002t0022g0101 a0001c0007t0008g0005 others(4): Show |
9 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.682+4672_682+4676d others(7): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119720405 | ||||||
chr3:119720410 | G | A | 1 | a0001c0002t0002g0047 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.682+4667G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720410 | |||||||
chr3:119720410 | GA | G | 62 | a0001c0001t0001g0150 a0001c0001t0001g0258 a0001c0001t0001g0279 others(59): Show |
66 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.682+4671delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119720410 | ||||||
chr3:119720411 | A | G | 2 | a0001c0002t0002g0047 a0001c0002t0002g0049 |
2 | HG03654.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.682+4668A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720411 | |||||||
chr3:119720539 | A | T | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.682+4796A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720539 | |||||||
chr3:119720541 | T | C | 8 | a0001c0002t0013g0048 a0001c0002t0013g0104 a0001c0002t0022g0101 others(5): Show |
10 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+4798T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720541 | |||||||
chr3:119720558 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.682+4815G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720558 | |||||||
chr3:119720573 | C | T | 1 | a0009c0022t0005g0324 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.682+4830C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720573 | |||||||
chr3:119720641 | A | G | 1 | a0001c0009t0001g0108 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.682+4898A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720641 | |||||||
chr3:119720722 | A | G | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.682+4979A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720722 | |||||||
chr3:119720742 | T | C | 1 | a0001c0003t0001g0330 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.682+4999T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720742 | |||||||
chr3:119720761 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.682+5018A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720761 | |||||||
chr3:119720801 | C | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.682+5058C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720801 | |||||||
chr3:119720820 | C | T | 1 | a0018c0019t0001g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.682+5077C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720820 | |||||||
chr3:119720822 | A | G | 1 | a0001c0002t0002g0056 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.682+5079A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720822 | |||||||
chr3:119720830 | C | T | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.682+5087C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720830 | |||||||
chr3:119720907 | T | C | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.682+5164T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119720907 | |||||||
chr3:119720930 | G | GA | 18 | a0001c0002t0013g0048 a0001c0002t0013g0104 a0001c0002t0022g0101 others(15): Show |
23 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.682+5193dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119720930 | ||||||
chr3:119721086 | C | CA | 5 | a0001c0002t0013g0048 a0001c0002t0013g0104 a0001c0002t0022g0101 others(2): Show |
6 | HG00735.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-5078dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119721086 | ||||||
chr3:119721146 | T | C | 5 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(2): Show |
7 | HG02615.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-5025T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721146 | |||||||
chr3:119721236 | G | C | 1 | a0001c0007t0008g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.683-4935G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721236 | |||||||
chr3:119721254 | C | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-4917C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721254 | |||||||
chr3:119721282 | G | A | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.683-4889G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721282 | |||||||
chr3:119721292 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.683-4879G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721292 | |||||||
chr3:119721457 | G | A | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-4714G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721457 | |||||||
chr3:119721494 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.683-4677C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721494 | |||||||
chr3:119721587 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0176 |
2 | NA18953.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.683-4584A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721587 | |||||||
chr3:119721621 | A | T | 3 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0002c0004t0004g0028 |
5 | HG02055.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-4550A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721621 | |||||||
chr3:119721776 | C | T | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.683-4395C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721776 | |||||||
chr3:119721843 | C | G | 242 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.683-4328C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721843 | |||||||
chr3:119721900 | G | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4271G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119721900 | |||||||
chr3:119722093 | C | G | 1 | a0001c0002t0002g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.683-4078C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722093 | |||||||
chr3:119722165 | C | T | 13 | a0001c0003t0004g0303 a0003c0005t0004g0111 a0003c0005t0004g0306 others(10): Show |
13 | HG01099.hp2 HG01106.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-4006C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722165 | |||||||
chr3:119722177 | T | TA | 23 | a0001c0001t0001g0114 a0001c0001t0001g0162 a0001c0001t0001g0163 others(20): Show |
23 | HG01257.hp2 HG01884.hp1 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.683-3976dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119722177 | ||||||
chr3:119722177 | T | TAA | 9 | a0001c0001t0001g0187 a0001c0002t0013g0104 a0001c0007t0008g0005 others(6): Show |
11 | HG00735.hp2 HG01891.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.683-3977_683-3976d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119722177 | ||||||
chr3:119722177 | T | TAAAAAA | 4 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0002c0004t0004g0028 others(1): Show |
6 | HG02055.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3981_683-3976d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119722177 | ||||||
chr3:119722177 | TA | T | 25 | a0001c0001t0001g0223 a0001c0001t0003g0113 a0001c0001t0003g0126 others(22): Show |
26 | HG00597.hp2 HG02083.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.683-3976delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119722177 | ||||||
chr3:119722195 | A | AAAAAAAA others(3): Show |
2 | a0005c0008t0007g0353 a0010c0015t0007g0159 |
2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.683-3976_683-3975i others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722195 | |||||||
chr3:119722195 | A | AAAAAAAA others(2): Show |
4 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(1): Show |
6 | HG02615.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3976_683-3975i others(11): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722195 | |||||||
chr3:119722244 | G | A | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-3927G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722244 | |||||||
chr3:119722314 | C | A | 1 | a0001c0003t0003g0320 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.683-3857C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722314 | |||||||
chr3:119722350 | T | A | 2 | a0001c0001t0003g0222 a0001c0002t0002g0086 |
2 | NA18952.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.683-3821T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722350 | |||||||
chr3:119722678 | G | A | 1 | a0009c0026t0032g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.683-3493G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722678 | |||||||
chr3:119722683 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.683-3488T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722683 | |||||||
chr3:119722907 | A | G | 1 | a0007c0011t0009g0247 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.683-3264A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722907 | |||||||
chr3:119722931 | A | G | 1 | a0003c0005t0004g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.683-3240A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722931 | |||||||
chr3:119722964 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.683-3207A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119722964 | |||||||
chr3:119723232 | G | A | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-2939G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723232 | |||||||
chr3:119723372 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.683-2799T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723372 | |||||||
chr3:119723391 | T | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.683-2780T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723391 | |||||||
chr3:119723398 | A | G | 1 | a0001c0001t0030g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.683-2773A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723398 | |||||||
chr3:119723421 | G | T | 1 | a0001c0009t0005g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.683-2750G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723421 | |||||||
chr3:119723540 | C | G | 3 | a0001c0002t0013g0048 a0001c0002t0013g0104 a0001c0002t0022g0101 |
3 | HG00735.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.683-2631C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723540 | |||||||
chr3:119723725 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
119 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.683-2446T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723725 | |||||||
chr3:119723798 | G | A | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-2373G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119723798 | |||||||
chr3:119724005 | C | CA | 9 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0002c0004t0004g0028 others(6): Show |
13 | HG02055.hp1 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-2157dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119724005 | ||||||
chr3:119724025 | G | A | 1 | a0001c0003t0029g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.683-2146G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724025 | |||||||
chr3:119724087 | G | A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.683-2084G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724087 | |||||||
chr3:119724108 | C | T | 3 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0002c0004t0004g0028 |
5 | HG02055.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-2063C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724108 | |||||||
chr3:119724168 | C | CA | 22 | a0001c0001t0001g0132 a0001c0001t0001g0201 a0001c0001t0001g0202 others(19): Show |
25 | HG00639.hp1 HG02258.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.683-1987dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119724168 | ||||||
chr3:119724168 | CA | C | 79 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0237 others(76): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.683-1987delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119724168 | ||||||
chr3:119724214 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.683-1957A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724214 | |||||||
chr3:119724258 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.683-1913G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724258 | |||||||
chr3:119724347 | G | A | 1 | a0011c0028t0006g0083 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.683-1824G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724347 | |||||||
chr3:119724394 | A | G | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.683-1777A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724394 | |||||||
chr3:119724411 | A | G | 3 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0002c0004t0004g0028 |
5 | HG02055.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-1760A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724411 | |||||||
chr3:119724527 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.683-1644T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724527 | |||||||
chr3:119724574 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0235 |
2 | NA19060.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.683-1597A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724574 | |||||||
chr3:119724744 | TTTTA | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 |
3 | HG01981.hp2 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.683-1418_683-1415d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119724744 | ||||||
chr3:119724830 | C | T | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-1341C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119724830 | |||||||
chr3:119724997 | GA | G | 9 | a0001c0001t0001g0158 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG01358.hp1 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.683-1171delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119724997 | ||||||
chr3:119725077 | GTATAAT | G | 74 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(71): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.683-1089_683-1084d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119725077 | ||||||
chr3:119725208 | A | G | 12 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(9): Show |
13 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.683-963A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725208 | |||||||
chr3:119725215 | T | C | 1 | a0001c0002t0002g0040 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.683-956T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725215 | |||||||
chr3:119725248 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.683-923G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725248 | |||||||
chr3:119725254 | G | A | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-917G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725254 | |||||||
chr3:119725363 | A | G | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-808A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725363 | |||||||
chr3:119725471 | G | A | 3 | a0003c0005t0004g0313 a0003c0005t0004g0314 a0003c0005t0004g0315 |
3 | HG01106.hp2 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.683-700G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725471 | |||||||
chr3:119725522 | G | A | 1 | a0001c0014t0016g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.683-649G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725522 | |||||||
chr3:119725580 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0265 others(3): Show |
6 | HG01255.hp1 HG01496.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-591C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725580 | |||||||
chr3:119725616 | G | A | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.683-555G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725616 | |||||||
chr3:119725765 | GA | G | 19 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0001c0003t0029g0326 others(16): Show |
25 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.683-395delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 119725765 | ||||||
chr3:119725799 | G | A | 18 | a0001c0003t0029g0326 a0002c0004t0005g0029 a0002c0004t0005g0335 others(15): Show |
19 | HG00639.hp1 HG01109.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-372G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725799 | |||||||
chr3:119725829 | C | A | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-342C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725829 | |||||||
chr3:119725926 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0258 |
2 | HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.683-245C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725926 | |||||||
chr3:119725967 | C | T | 346 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(343): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.683-204C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119725967 | |||||||
chr3:119726167 | G | A | 1 | a0001c0001t0003g0113 | 1 | NA19080.hp1 | splice_region_variant&intron_variant | LOW | c.683-4G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 6/17 | chr3 | 119726167 | |||||||
chr3:119726354 | T | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0118 others(14): Show |
19 | HG00423.hp1 HG00621.hp2 HG02027.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.860+6T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119726354 | |||||||
chr3:119726421 | C | T | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.860+73C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119726421 | |||||||
chr3:119726888 | A | C | 77 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(74): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.860+540A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119726888 | |||||||
chr3:119727004 | T | C | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.860+656T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727004 | |||||||
chr3:119727007 | T | C | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.860+659T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727007 | |||||||
chr3:119727083 | C | G | 2 | a0001c0002t0013g0048 a0001c0002t0013g0104 |
2 | HG00735.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.860+735C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727083 | |||||||
chr3:119727084 | T | C | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.860+736T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727084 | |||||||
chr3:119727203 | G | A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.860+855G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727203 | |||||||
chr3:119727267 | T | G | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.860+919T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727267 | |||||||
chr3:119727460 | A | G | 9 | a0001c0014t0016g0109 a0001c0014t0016g0110 a0005c0008t0007g0004 others(6): Show |
11 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.860+1112A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727460 | |||||||
chr3:119727544 | C | G | 1 | a0001c0001t0003g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.860+1196C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727544 | |||||||
chr3:119727594 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
119 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.860+1246A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727594 | |||||||
chr3:119727658 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 |
3 | HG01981.hp2 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.860+1310G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727658 | |||||||
chr3:119727759 | C | T | 2 | a0001c0009t0001g0107 a0001c0009t0001g0108 |
2 | HG01123.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.860+1411C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727759 | |||||||
chr3:119727858 | G | A | 346 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(343): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.860+1510G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727858 | |||||||
chr3:119727920 | A | G | 1 | a0001c0001t0025g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.860+1572A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119727920 | |||||||
chr3:119728013 | AATG | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.860+1689_860+1691d others(5): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 119728013 | ||||||
chr3:119728013 | AATGATG | A | 17 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(14): Show |
20 | HG00639.hp1 HG02258.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.860+1686_860+1691d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 119728013 | ||||||
chr3:119728015 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(187): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.860+1667T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728015 | |||||||
chr3:119728062 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0130 others(1): Show |
4 | HG02027.hp1 HG02080.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.860+1714T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728062 | |||||||
chr3:119728087 | A | G | 1 | a0001c0002t0006g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.860+1739A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728087 | |||||||
chr3:119728088 | G | A | 1 | a0001c0003t0004g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.860+1740G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728088 | |||||||
chr3:119728089 | T | A | 1 | a0001c0003t0004g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.860+1741T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728089 | |||||||
chr3:119728116 | A | G | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.860+1768A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728116 | |||||||
chr3:119728124 | G | A | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.860+1776G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728124 | |||||||
chr3:119728127 | A | AATG | 38 | a0001c0002t0013g0048 a0001c0002t0013g0104 a0001c0002t0022g0101 others(35): Show |
42 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.860+1787_860+1789d others(5): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 119728127 | ||||||
chr3:119728127 | A | G | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.860+1779A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728127 | |||||||
chr3:119728280 | A | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.860+1932A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728280 | |||||||
chr3:119728308 | G | A | 2 | a0001c0003t0003g0327 a0001c0003t0003g0329 |
2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.861-1912G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728308 | |||||||
chr3:119728440 | A | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.861-1780A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728440 | |||||||
chr3:119728451 | C | CA | 12 | a0003c0005t0004g0111 a0003c0005t0004g0306 a0003c0005t0004g0307 others(9): Show |
12 | HG01099.hp2 HG01106.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-1768dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 119728451 | ||||||
chr3:119728659 | A | G | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.861-1561A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728659 | |||||||
chr3:119728803 | G | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0244 a0001c0001t0001g0290 |
4 | HG00099.hp1 HG00323.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-1417G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728803 | |||||||
chr3:119728877 | T | G | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.861-1343T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728877 | |||||||
chr3:119728888 | G | A | 4 | a0007c0011t0009g0245 a0007c0011t0009g0246 a0007c0011t0009g0247 others(1): Show |
4 | HG00597.hp1 NA18994.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-1332G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728888 | |||||||
chr3:119728890 | A | G | 11 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(8): Show |
12 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.861-1330A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119728890 | |||||||
chr3:119729000 | G | A | 12 | a0003c0005t0004g0111 a0003c0005t0004g0306 a0003c0005t0004g0307 others(9): Show |
12 | HG01099.hp2 HG01106.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-1220G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729000 | |||||||
chr3:119729026 | A | G | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.861-1194A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729026 | |||||||
chr3:119729192 | A | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.861-1028A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729192 | |||||||
chr3:119729213 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
6 | NA18612.hp1 NA18612.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.861-1007C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729213 | |||||||
chr3:119729233 | C | T | 1 | a0001c0002t0002g0047 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.861-987C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729233 | |||||||
chr3:119729266 | G | A | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.861-954G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729266 | |||||||
chr3:119729536 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.861-684C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729536 | |||||||
chr3:119729559 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.861-661G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729559 | |||||||
chr3:119729944 | C | T | 9 | a0001c0014t0016g0109 a0001c0014t0016g0110 a0005c0008t0007g0004 others(6): Show |
11 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.861-276C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119729944 | |||||||
chr3:119730185 | C | T | 1 | a0001c0002t0006g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.861-35C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 7/17 | chr3 | 119730185 | |||||||
chr3:119730601 | A | AGT | 4 | a0001c0001t0001g0266 a0001c0001t0001g0289 a0001c0001t0030g0224 others(1): Show |
4 | HG01255.hp1 NA18962.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018+272_1018+273d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGT | 4 | a0001c0001t0001g0223 a0001c0001t0001g0267 a0002c0004t0001g0344 others(1): Show |
5 | HG01496.hp1 HG02809.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018+270_1018+273d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGTGT | 6 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0003t0018g0332 others(3): Show |
6 | HG02055.hp2 HG02155.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018+268_1018+273d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGTGTG others(1): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0183 a0001c0001t0001g0210 others(2): Show |
5 | HG02129.hp1 HG03239.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018+266_1018+273d others(10): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGTGTG others(3): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0178 a0001c0001t0001g0193 others(6): Show |
9 | HG00423.hp2 HG00609.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1018+264_1018+273d others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0020 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG02015.hp2 NA18944.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018+262_1018+273d others(14): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0237 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1018+260_1018+273d others(16): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0001g0196 a0001c0001t0001g0207 |
2 | HG02135.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1018+258_1018+273d others(18): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | A | AGTGTGTG others(11): Show |
1 | a0018c0019t0001g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1018+256_1018+273d others(20): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGT | A | 48 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(45): Show |
51 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1018+272_1018+273d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGT | A | 42 | a0001c0001t0001g0016 a0001c0001t0001g0114 a0001c0001t0001g0177 others(39): Show |
46 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1018+270_1018+273d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGT | A | 65 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0022 others(62): Show |
70 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.1018+268_1018+273d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGTG others(1): Show |
A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1018+266_1018+273d others(10): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGTG others(3): Show |
A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0139 others(3): Show |
6 | HG00621.hp2 HG03453.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018+264_1018+273d others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGTG others(5): Show |
A | 18 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0001c0002t0002g0054 others(15): Show |
20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1018+262_1018+273d others(14): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGTG others(7): Show |
A | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0032 others(5): Show |
10 | HG01891.hp2 HG02602.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1018+260_1018+273d others(16): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGTG others(11): Show |
A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1018+256_1018+273d others(20): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGTG others(13): Show |
A | 1 | a0001c0002t0013g0104 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1018+254_1018+273d others(22): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730601 | AGTGTGTG others(15): Show |
A | 2 | a0001c0002t0013g0048 a0001c0002t0022g0101 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1018+252_1018+273d others(24): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 119730601 | ||||||
chr3:119730650 | G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0235 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1018+273_1018+274i others(17): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119730650 | |||||||
chr3:119730975 | A | G | 137 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(134): Show |
152 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1018+598A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119730975 | |||||||
chr3:119731100 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1018+723T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119731100 | |||||||
chr3:119731265 | T | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1018+888T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119731265 | |||||||
chr3:119731379 | A | G | 1 | a0001c0007t0008g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1019-915A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119731379 | |||||||
chr3:119731447 | T | C | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1019-847T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119731447 | |||||||
chr3:119731747 | C | G | 74 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(71): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1019-547C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119731747 | |||||||
chr3:119731817 | C | T | 1 | a0001c0001t0003g0155 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1019-477C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119731817 | |||||||
chr3:119732030 | CA | C | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1019-263delA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119732030 | |||||||
chr3:119732124 | A | G | 7 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0032 others(4): Show |
9 | HG01891.hp2 HG02602.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1019-170A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119732124 | |||||||
chr3:119732218 | G | C | 1 | a0006c0010t0014g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1019-76G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 8/17 | chr3 | 119732218 | |||||||
chr3:119732847 | A | G | 90 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(87): Show |
99 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1201+371A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 9/17 | chr3 | 119732847 | |||||||
chr3:119732901 | A | G | 4 | a0001c0002t0002g0091 a0001c0002t0002g0096 a0001c0002t0002g0098 others(1): Show |
4 | NA18983.hp2 NA18990.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201+425A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 9/17 | chr3 | 119732901 | |||||||
chr3:119732973 | G | A | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1202-391G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 9/17 | chr3 | 119732973 | |||||||
chr3:119732977 | C | G | 1 | a0001c0002t0006g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1202-387C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 9/17 | chr3 | 119732977 | |||||||
chr3:119733632 | T | C | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1344+126T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119733632 | |||||||
chr3:119733645 | A | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+139A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119733645 | |||||||
chr3:119733712 | T | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG01192.hp1 HG03491.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+206T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119733712 | |||||||
chr3:119733757 | T | C | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+251T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119733757 | |||||||
chr3:119733858 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
5 | HG01175.hp2 HG01243.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344+352A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119733858 | |||||||
chr3:119733883 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1344+377A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119733883 | |||||||
chr3:119734035 | G | T | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1344+529G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734035 | |||||||
chr3:119734233 | C | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1344+727C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734233 | |||||||
chr3:119734304 | T | C | 1 | a0001c0002t0002g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1344+798T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734304 | |||||||
chr3:119734336 | T | C | 1 | a0001c0002t0019g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1344+830T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734336 | |||||||
chr3:119734379 | C | A | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1344+873C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734379 | |||||||
chr3:119734465 | G | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+959G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734465 | |||||||
chr3:119734468 | G | GTTCCC | 341 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1344+965_1344+966i others(7): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 119734468 | ||||||
chr3:119734647 | A | G | 1 | a0001c0002t0006g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1344+1141A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734647 | |||||||
chr3:119734654 | A | G | 1 | a0006c0010t0033g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1344+1148A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734654 | |||||||
chr3:119734706 | A | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | NA19002.hp1 NA19055.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1344+1200A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734706 | |||||||
chr3:119734750 | C | G | 1 | a0001c0003t0001g0328 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1344+1244C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734750 | |||||||
chr3:119734890 | A | C | 4 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0046 others(1): Show |
4 | NA18944.hp1 NA18952.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+1384A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734890 | |||||||
chr3:119734993 | T | G | 76 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(73): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1344+1487T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119734993 | |||||||
chr3:119735060 | A | G | 1 | a0001c0001t0027g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1344+1554A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735060 | |||||||
chr3:119735168 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1344+1662G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735168 | |||||||
chr3:119735187 | A | G | 2 | a0009c0022t0005g0324 a0009c0026t0032g0099 |
2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1344+1681A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735187 | |||||||
chr3:119735381 | A | G | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344+1875A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735381 | |||||||
chr3:119735574 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1345-1792A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735574 | |||||||
chr3:119735575 | T | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0178 others(26): Show |
31 | HG00423.hp2 HG00609.hp2 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.1345-1791T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735575 | |||||||
chr3:119735669 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1345-1697A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735669 | |||||||
chr3:119735727 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1345-1639A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735727 | |||||||
chr3:119735746 | C | T | 1 | a0001c0003t0029g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1345-1620C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735746 | |||||||
chr3:119735869 | G | C | 1 | a0001c0001t0001g0219 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1345-1497G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119735869 | |||||||
chr3:119735909 | TCTTATA | T | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-1450_1345-144 others(10): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 119735909 | ||||||
chr3:119735968 | CT | C | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-1386delT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 119735968 | ||||||
chr3:119736053 | C | CG | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345-1307dupG | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 119736053 | ||||||
chr3:119736268 | G | GT | 99 | a0001c0001t0001g0141 a0001c0001t0001g0162 a0001c0001t0001g0163 others(96): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1345-1077dupT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 119736268 | ||||||
chr3:119736268 | G | GTT | 11 | a0001c0002t0002g0047 a0001c0002t0002g0072 a0001c0003t0003g0325 others(8): Show |
11 | HG01243.hp1 HG02622.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.1345-1078_1345-107 others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 119736268 | ||||||
chr3:119736269 | T | TTTTTTTT others(1): Show |
6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345-1090_1345-108 others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 119736269 | ||||||
chr3:119736274 | T | G | 1 | a0002c0004t0005g0349 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1345-1092T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736274 | |||||||
chr3:119736303 | A | T | 1 | a0001c0002t0013g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1345-1063A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736303 | |||||||
chr3:119736467 | G | A | 1 | a0001c0002t0002g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1345-899G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736467 | |||||||
chr3:119736493 | G | A | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1345-873G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736493 | |||||||
chr3:119736555 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1345-811C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736555 | |||||||
chr3:119736739 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1345-627G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736739 | |||||||
chr3:119736938 | G | A | 27 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0178 others(24): Show |
29 | HG00423.hp2 HG00609.hp2 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.1345-428G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736938 | |||||||
chr3:119736944 | C | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345-422C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119736944 | |||||||
chr3:119737278 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1345-88C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 10/17 | chr3 | 119737278 | |||||||
chr3:119737949 | A | G | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1461+467A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119737949 | |||||||
chr3:119737992 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1461+510A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119737992 | |||||||
chr3:119738152 | G | A | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1461+670G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738152 | |||||||
chr3:119738265 | C | T | 3 | a0001c0007t0008g0006 a0001c0013t0015g0186 a0001c0013t0028g0185 |
4 | HG02602.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1461+783C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738265 | |||||||
chr3:119738330 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0012g0123 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1461+849_1461+850i others(20): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738330 | ||||||
chr3:119738330 | G | GTTTTTTT others(12): Show |
1 | a0001c0001t0012g0124 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1461+849_1461+850i others(21): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738330 | ||||||
chr3:119738332 | C | CT | 41 | a0001c0001t0001g0239 a0001c0001t0001g0248 a0001c0001t0001g0249 others(38): Show |
44 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1461+884dupT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTT | 23 | a0001c0001t0001g0019 a0001c0001t0001g0250 a0001c0001t0001g0299 others(20): Show |
27 | HG00423.hp2 HG00741.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.1461+883_1461+884d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTT | 16 | a0001c0001t0001g0187 a0001c0001t0001g0235 a0001c0001t0001g0291 others(13): Show |
16 | HG00621.hp1 HG01123.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1461+882_1461+884d others(5): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTT | 8 | a0001c0001t0001g0114 a0001c0001t0001g0179 a0001c0003t0001g0328 others(5): Show |
9 | HG00738.hp1 HG01258.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1461+881_1461+884d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0112 others(15): Show |
21 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1461+880_1461+884d others(7): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTT | 29 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(26): Show |
33 | HG00544.hp2 HG00621.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1461+879_1461+884d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT | 20 | a0001c0001t0001g0117 a0001c0001t0001g0121 a0001c0001t0001g0122 others(17): Show |
20 | HG00408.hp1 HG01109.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1461+878_1461+884d others(9): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1461+875_1461+884d others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0020 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
5 | HG02015.hp2 HG02074.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1461+872_1461+884d others(15): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(7): Show |
6 | a0001c0001t0001g0196 a0001c0001t0001g0207 a0001c0001t0001g0236 others(3): Show |
6 | HG01943.hp1 HG02135.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+871_1461+884d others(16): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(8): Show |
7 | a0001c0001t0001g0024 a0001c0001t0001g0232 a0001c0001t0001g0279 others(4): Show |
8 | HG01884.hp1 NA18966.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461+870_1461+884d others(17): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0189 a0001c0001t0001g0242 |
2 | NA19000.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1461+869_1461+884d others(18): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0264 a0001c0001t0001g0284 |
3 | HG02129.hp1 NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1461+868_1461+884d others(19): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(11): Show |
8 | a0001c0001t0001g0115 a0001c0001t0001g0166 a0001c0001t0001g0171 others(5): Show |
8 | HG00609.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461+867_1461+884d others(20): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(12): Show |
17 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0169 others(14): Show |
18 | HG00738.hp2 HG01192.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1461+866_1461+884d others(21): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(13): Show |
21 | a0001c0001t0001g0010 a0001c0001t0001g0156 a0001c0001t0001g0157 others(18): Show |
22 | HG01074.hp2 HG01106.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1461+865_1461+884d others(22): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(14): Show |
9 | a0001c0001t0001g0177 a0001c0001t0001g0200 a0001c0001t0001g0202 others(6): Show |
9 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1461+864_1461+884d others(23): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0301 |
2 | HG01099.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1461+863_1461+884d others(24): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1461+862_1461+884d others(25): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0225 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1461+861_1461+884d others(26): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1461+859_1461+884d others(28): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1461+852_1461+884d others(35): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | C | T | 2 | a0001c0001t0012g0123 a0001c0001t0012g0124 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1461+850C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738332 | |||||||
chr3:119738332 | CT | C | 6 | a0001c0001t0011g0298 a0001c0001t0027g0190 a0003c0005t0004g0111 others(3): Show |
6 | HG01069.hp1 HG01106.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+884delT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTT | C | 9 | a0001c0001t0001g0178 a0001c0002t0002g0067 a0003c0005t0004g0306 others(6): Show |
9 | HG02280.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1461+883_1461+884d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTT | C | 6 | a0001c0001t0001g0205 a0001c0002t0002g0075 a0001c0002t0002g0084 others(3): Show |
6 | HG00558.hp2 HG01099.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+882_1461+884d others(5): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTT | C | 12 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.1461+881_1461+884d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTT | C | 14 | a0001c0001t0001g0131 a0001c0001t0001g0172 a0001c0001t0001g0174 others(11): Show |
16 | HG02040.hp1 HG02165.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1461+880_1461+884d others(7): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTT | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0198 a0001c0001t0001g0213 others(3): Show |
6 | HG00544.hp1 HG02647.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+879_1461+884d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0282 a0001c0002t0002g0038 others(4): Show |
7 | HG00408.hp2 HG00597.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1461+878_1461+884d others(9): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(2): Show |
C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0183 a0001c0002t0013g0048 others(8): Show |
14 | HG00735.hp2 HG01070.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1461+876_1461+884d others(11): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0023 a0001c0001t0030g0224 a0001c0009t0005g0009 others(1): Show |
6 | HG00099.hp1 HG00323.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+875_1461+884d others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0253 a0004c0006t0001g0204 a0008c0012t0010g0309 others(3): Show |
6 | HG02622.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+874_1461+884d others(13): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0238 a0001c0001t0001g0296 others(1): Show |
4 | HG02109.hp2 HG02698.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1461+873_1461+884d others(14): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0001g0240 a0001c0001t0001g0243 a0001c0003t0001g0305 |
3 | HG03486.hp2 NA19005.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1461+870_1461+884d others(17): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(9): Show |
C | 1 | a0001c0003t0001g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1461+869_1461+884d others(18): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0128 a0001c0001t0001g0151 |
4 | HG00558.hp1 HG02129.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1461+867_1461+884d others(20): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738332 | CTTTTTTT others(14): Show |
C | 3 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0002c0004t0004g0028 |
5 | HG02055.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1461+864_1461+884d others(23): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 119738332 | ||||||
chr3:119738379 | C | T | 90 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(87): Show |
99 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1462-876C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738379 | |||||||
chr3:119738399 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1462-856A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738399 | |||||||
chr3:119738496 | G | A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1462-759G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738496 | |||||||
chr3:119738539 | G | C | 1 | a0001c0001t0001g0261 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1462-716G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738539 | |||||||
chr3:119738776 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1462-479G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738776 | |||||||
chr3:119738931 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1462-324A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 11/17 | chr3 | 119738931 | |||||||
chr3:119739575 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0152 |
2 | NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1533+249A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 12/17 | chr3 | 119739575 | |||||||
chr3:119739598 | TCTTC | T | 92 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(89): Show |
101 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1533+276_1533+279d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr3 | 119739598 | ||||||
chr3:119740004 | C | T | 92 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(89): Show |
101 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1534-545C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 12/17 | chr3 | 119740004 | |||||||
chr3:119740026 | A | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1534-523A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 12/17 | chr3 | 119740026 | |||||||
chr3:119740168 | C | A | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1534-381C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 12/17 | chr3 | 119740168 | |||||||
chr3:119740792 | A | T | 74 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(71): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1680+97A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119740792 | |||||||
chr3:119740835 | T | TGTGTGTG others(4): Show |
1 | a0001c0002t0002g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1680+140_1680+141i others(13): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119740835 | |||||||
chr3:119740835 | T | TGTGTGTG others(6): Show |
1 | a0001c0002t0002g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1680+140_1680+141i others(15): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119740835 | |||||||
chr3:119740835 | T | TTG | 114 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0024 others(111): Show |
123 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1680+179_1680+180d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTG | 41 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(38): Show |
47 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.1680+177_1680+180d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTGTG | 12 | a0001c0001t0001g0132 a0001c0002t0002g0042 a0001c0002t0002g0102 others(9): Show |
14 | HG01123.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1680+175_1680+180d others(8): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTGTGT others(1): Show |
7 | a0001c0002t0002g0001 a0001c0002t0002g0040 a0001c0002t0002g0041 others(4): Show |
9 | HG00639.hp2 HG01081.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1680+173_1680+180d others(10): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTGTGT others(3): Show |
36 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(33): Show |
38 | HG00099.hp2 HG00597.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1680+171_1680+180d others(12): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTGTGT others(5): Show |
17 | a0001c0001t0001g0263 a0001c0002t0002g0038 a0001c0002t0002g0052 others(14): Show |
17 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1680+169_1680+180d others(14): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTGTGT others(7): Show |
2 | a0001c0002t0002g0039 a0001c0002t0002g0093 |
2 | HG00609.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1680+167_1680+180d others(16): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTGTGT others(9): Show |
1 | a0001c0002t0002g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1680+165_1680+180d others(18): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | T | TTGTGTGT others(11): Show |
1 | a0001c0002t0002g0055 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1680+163_1680+180d others(20): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | TTG | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
65 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1680+179_1680+180d others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740835 | TTGTG | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0166 others(2): Show |
5 | HG00323.hp1 HG00558.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1680+177_1680+180d others(6): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119740835 | ||||||
chr3:119740906 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | NA18986.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1680+211G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119740906 | |||||||
chr3:119740969 | T | C | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1680+274T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119740969 | |||||||
chr3:119741024 | G | A | 1 | a0001c0002t0013g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1680+329G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741024 | |||||||
chr3:119741059 | C | A | 1 | a0003c0005t0004g0334 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1680+364C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741059 | |||||||
chr3:119741071 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1680+376C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741071 | |||||||
chr3:119741167 | T | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1680+472T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741167 | |||||||
chr3:119741280 | T | C | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1680+585T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741280 | |||||||
chr3:119741483 | C | T | 1 | a0003c0005t0004g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1680+788C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741483 | |||||||
chr3:119741546 | C | T | 11 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(8): Show |
12 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1680+851C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741546 | |||||||
chr3:119741678 | G | C | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1680+983G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741678 | |||||||
chr3:119741992 | T | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1680+1297T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119741992 | |||||||
chr3:119742002 | G | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1680+1307G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742002 | |||||||
chr3:119742006 | A | G | 1 | a0001c0002t0002g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1680+1311A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742006 | |||||||
chr3:119742081 | A | AG | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1680+1387dupG | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119742081 | ||||||
chr3:119742312 | A | G | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1680+1617A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742312 | |||||||
chr3:119742327 | G | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1680+1632G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742327 | |||||||
chr3:119742504 | G | A | 2 | a0001c0003t0001g0304 a0001c0003t0001g0305 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1681-1471G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742504 | |||||||
chr3:119742649 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0264 |
2 | NA19000.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1681-1326G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742649 | |||||||
chr3:119742821 | G | A | 1 | a0001c0002t0013g0104 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1681-1154G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742821 | |||||||
chr3:119742839 | A | G | 1 | a0003c0005t0004g0313 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1681-1136A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742839 | |||||||
chr3:119742845 | T | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0022 others(19): Show |
25 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1681-1130T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742845 | |||||||
chr3:119742995 | A | G | 1 | a0007c0011t0009g0246 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1681-980A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119742995 | |||||||
chr3:119743082 | G | A | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-893G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743082 | |||||||
chr3:119743087 | C | T | 10 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(7): Show |
11 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1681-888C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743087 | |||||||
chr3:119743134 | CT | C | 11 | a0001c0001t0001g0214 a0001c0007t0008g0005 a0001c0007t0008g0006 others(8): Show |
13 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1681-824delT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119743134 | ||||||
chr3:119743159 | G | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1681-816G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743159 | |||||||
chr3:119743265 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1681-710G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743265 | |||||||
chr3:119743290 | G | GT | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-684dupT | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 119743290 | ||||||
chr3:119743343 | C | G | 1 | a0009c0022t0005g0324 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1681-632C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743343 | |||||||
chr3:119743363 | C | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-612C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743363 | |||||||
chr3:119743393 | C | T | 1 | a0003c0005t0004g0313 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1681-582C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743393 | |||||||
chr3:119743791 | G | A | 1 | a0001c0013t0028g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1681-184G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743791 | |||||||
chr3:119743802 | T | G | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1681-173T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743802 | |||||||
chr3:119743826 | G | A | 2 | a0001c0002t0013g0048 a0001c0002t0013g0104 |
2 | HG00735.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1681-149G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743826 | |||||||
chr3:119743948 | C | T | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1681-27C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 13/17 | chr3 | 119743948 | |||||||
chr3:119744341 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1902+145G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744341 | |||||||
chr3:119744351 | G | A | 4 | a0008c0012t0010g0309 a0008c0012t0010g0310 a0008c0012t0010g0311 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1902+155G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744351 | |||||||
chr3:119744429 | C | A | 134 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(131): Show |
149 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1902+233C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744429 | |||||||
chr3:119744594 | C | T | 1 | a0001c0007t0008g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1902+398C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744594 | |||||||
chr3:119744619 | T | A | 16 | a0003c0005t0004g0318 a0005c0008t0007g0004 a0005c0008t0007g0351 others(13): Show |
18 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1902+423T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744619 | |||||||
chr3:119744719 | C | G | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1902+523C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744719 | |||||||
chr3:119744764 | A | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0001c0001t0001g0256 |
4 | NA18942.hp1 NA18998.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1902+568A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744764 | |||||||
chr3:119744795 | C | G | 1 | a0001c0002t0002g0092 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1902+599C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119744795 | |||||||
chr3:119745331 | A | G | 4 | a0008c0012t0010g0309 a0008c0012t0010g0310 a0008c0012t0010g0311 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1902+1135A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119745331 | |||||||
chr3:119745361 | A | G | 1 | a0001c0002t0020g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1902+1165A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119745361 | |||||||
chr3:119745410 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1902+1214A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119745410 | |||||||
chr3:119745616 | C | T | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1902+1420C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119745616 | |||||||
chr3:119745870 | C | T | 20 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(17): Show |
21 | HG00597.hp2 HG02083.hp1 NA18944.hp1 others(18): Show |
intron_variant | MODIFIER | c.1903-1245C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119745870 | |||||||
chr3:119746439 | A | G | 1 | a0002c0004t0005g0349 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1903-676A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119746439 | |||||||
chr3:119746682 | C | G | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1903-433C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119746682 | |||||||
chr3:119746767 | A | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1903-348A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119746767 | |||||||
chr3:119746768 | G | C | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1903-347G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119746768 | |||||||
chr3:119746809 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1903-306G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119746809 | |||||||
chr3:119747076 | G | A | 1 | a0001c0007t0008g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1903-39G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 14/17 | chr3 | 119747076 | |||||||
chr3:119747446 | A | C | 3 | a0001c0003t0029g0326 a0001c0014t0016g0109 a0001c0014t0016g0110 |
3 | HG02698.hp2 HG03927.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2051+183A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 15/17 | chr3 | 119747446 | |||||||
chr3:119747465 | G | A | 1 | a0002c0004t0005g0029 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2051+202G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 15/17 | chr3 | 119747465 | |||||||
chr3:119747531 | A | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2051+268A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 15/17 | chr3 | 119747531 | |||||||
chr3:119747628 | T | A | 1 | a0001c0003t0029g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2052-183T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 15/17 | chr3 | 119747628 | |||||||
chr3:119747778 | A | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2052-33A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 15/17 | chr3 | 119747778 | |||||||
chr3:119747978 | T | C | 1 | a0006c0010t0014g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2143+76T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119747978 | |||||||
chr3:119747979 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2143+77T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119747979 | |||||||
chr3:119748011 | G | T | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2143+109G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748011 | |||||||
chr3:119748057 | C | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2143+155C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748057 | |||||||
chr3:119748081 | A | G | 3 | a0001c0001t0004g0014 a0001c0001t0004g0160 a0002c0004t0004g0028 |
5 | HG02055.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2143+179A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748081 | |||||||
chr3:119748268 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2143+366G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748268 | |||||||
chr3:119748292 | A | G | 347 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(344): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.2143+390A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748292 | |||||||
chr3:119748390 | A | G | 7 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0032 others(4): Show |
9 | HG01891.hp2 HG02602.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2143+488A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748390 | |||||||
chr3:119748649 | A | G | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2143+747A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748649 | |||||||
chr3:119748855 | C | A | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2143+953C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119748855 | |||||||
chr3:119749189 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2143+1287C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119749189 | |||||||
chr3:119749454 | G | A | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-1483G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119749454 | |||||||
chr3:119749566 | G | A | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2144-1371G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119749566 | |||||||
chr3:119749618 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG01258.hp2 HG01261.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.2144-1319G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119749618 | |||||||
chr3:119749631 | A | G | 1 | a0001c0001t0003g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2144-1306A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119749631 | |||||||
chr3:119749706 | G | A | 1 | a0001c0001t0027g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2144-1231G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119749706 | |||||||
chr3:119749919 | A | G | 1 | a0001c0003t0003g0026 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2144-1018A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119749919 | |||||||
chr3:119750139 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2144-798C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750139 | |||||||
chr3:119750171 | G | A | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2144-766G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750171 | |||||||
chr3:119750398 | G | A | 20 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(17): Show |
21 | HG00597.hp2 HG02083.hp1 NA18944.hp1 others(18): Show |
intron_variant | MODIFIER | c.2144-539G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750398 | |||||||
chr3:119750402 | A | G | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.2144-535A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750402 | |||||||
chr3:119750434 | C | T | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2144-503C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750434 | |||||||
chr3:119750561 | C | A | 1 | a0001c0003t0003g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2144-376C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750561 | |||||||
chr3:119750592 | C | T | 77 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(74): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.2144-345C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750592 | |||||||
chr3:119750619 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2144-318C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 16/17 | chr3 | 119750619 | |||||||
chr3:119751173 | TCAAA | T | 20 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(17): Show |
21 | HG00597.hp2 HG02083.hp1 NA18944.hp1 others(18): Show |
intron_variant | MODIFIER | c.*1+79_*1+82delACAA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 119751173 | ||||||
chr3:119751198 | C | A | 1 | a0001c0007t0008g0032 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*1+100C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751198 | |||||||
chr3:119751214 | G | A | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.*1+116G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751214 | |||||||
chr3:119751308 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.*1+210C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751308 | |||||||
chr3:119751728 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
5 | NA18946.hp2 NA18957.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+630C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751728 | |||||||
chr3:119751732 | G | A | 4 | a0001c0002t0002g0091 a0001c0002t0002g0096 a0001c0002t0002g0098 others(1): Show |
4 | NA18983.hp2 NA18990.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1+634G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751732 | |||||||
chr3:119751779 | G | C | 5 | a0001c0001t0003g0116 a0001c0001t0003g0126 a0001c0001t0003g0161 others(2): Show |
5 | HG00597.hp2 NA18991.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+681G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751779 | |||||||
chr3:119751862 | C | T | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.*1+764C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751862 | |||||||
chr3:119751907 | C | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | NA19002.hp1 NA19055.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.*1+809C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751907 | |||||||
chr3:119751933 | A | T | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.*1+835A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119751933 | |||||||
chr3:119752029 | A | G | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.*1+931A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752029 | |||||||
chr3:119752212 | A | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*1+1114A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752212 | |||||||
chr3:119752334 | A | G | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*1+1236A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752334 | |||||||
chr3:119752361 | T | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0118 others(15): Show |
20 | HG00423.hp1 HG00621.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.*1+1263T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752361 | |||||||
chr3:119752549 | C | G | 1 | a0006c0010t0014g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*1+1451C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752549 | |||||||
chr3:119752556 | C | G | 2 | a0001c0002t0002g0084 a0001c0002t0021g0069 |
2 | HG00558.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.*1+1458C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752556 | |||||||
chr3:119752626 | T | C | 89 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(86): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.*1+1528T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752626 | |||||||
chr3:119752636 | A | G | 4 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0046 others(1): Show |
4 | NA18944.hp1 NA18952.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.*1+1538A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752636 | |||||||
chr3:119752840 | G | A | 7 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.*1+1742G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752840 | |||||||
chr3:119752941 | C | G | 2 | a0001c0002t0002g0091 a0001c0002t0002g0096 |
2 | NA18983.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.*1+1843C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752941 | |||||||
chr3:119752988 | G | A | 89 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(86): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.*1+1890G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119752988 | |||||||
chr3:119753113 | G | A | 2 | a0001c0003t0003g0327 a0001c0003t0003g0329 |
2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.*1+2015G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753113 | |||||||
chr3:119753154 | C | T | 1 | a0001c0002t0002g0056 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.*1+2056C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753154 | |||||||
chr3:119753324 | T | A | 1 | a0016c0018t0001g0133 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*1+2226T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753324 | |||||||
chr3:119753327 | G | A | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*1+2229G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753327 | |||||||
chr3:119753436 | A | C | 1 | a0001c0003t0003g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.*1+2338A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753436 | |||||||
chr3:119753480 | T | A | 107 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(104): Show |
114 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.*1+2382T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753480 | |||||||
chr3:119753746 | TG | T | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.*1+2650delG | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 119753746 | ||||||
chr3:119753798 | A | G | 1 | a0009c0022t0005g0324 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*1+2700A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753798 | |||||||
chr3:119753873 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.*1+2775A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119753873 | |||||||
chr3:119754008 | T | C | 1 | a0001c0001t0024g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.*1+2910T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754008 | |||||||
chr3:119754204 | A | G | 73 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(70): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.*1+3106A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754204 | |||||||
chr3:119754260 | C | G | 1 | a0003c0005t0004g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*1+3162C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754260 | |||||||
chr3:119754423 | A | G | 1 | a0001c0002t0006g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.*1+3325A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754423 | |||||||
chr3:119754543 | A | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*1+3445A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754543 | |||||||
chr3:119754594 | A | C | 8 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0030 others(5): Show |
10 | HG01891.hp2 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.*1+3496A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754594 | |||||||
chr3:119754698 | C | T | 1 | a0006c0010t0033g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*1+3600C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754698 | |||||||
chr3:119754814 | C | T | 2 | a0001c0003t0001g0304 a0001c0003t0001g0305 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.*1+3716C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754814 | |||||||
chr3:119754872 | T | C | 136 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(133): Show |
151 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.*1+3774T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754872 | |||||||
chr3:119754989 | C | T | 39 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0022 others(36): Show |
42 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.*1+3891C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119754989 | |||||||
chr3:119755297 | G | A | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.*1+4199G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755297 | |||||||
chr3:119755373 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*1+4275G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755373 | |||||||
chr3:119755374 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*1+4276A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755374 | |||||||
chr3:119755473 | C | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*1+4375C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755473 | |||||||
chr3:119755526 | C | T | 91 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(88): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.*1+4428C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755526 | |||||||
chr3:119755537 | A | G | 1 | a0006c0010t0014g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*1+4439A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755537 | |||||||
chr3:119755686 | A | G | 1 | a0003c0005t0004g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*1+4588A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755686 | |||||||
chr3:119755849 | G | A | 1 | a0003c0005t0004g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*1+4751G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755849 | |||||||
chr3:119755948 | T | C | 1 | a0001c0003t0029g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*1+4850T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755948 | |||||||
chr3:119755975 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*1+4877C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119755975 | |||||||
chr3:119756007 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.*1+4909A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756007 | |||||||
chr3:119756069 | A | G | 2 | a0001c0002t0013g0048 a0001c0002t0013g0104 |
2 | HG00735.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.*1+4971A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756069 | |||||||
chr3:119756122 | G | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*1+5024G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756122 | |||||||
chr3:119756205 | C | T | 12 | a0001c0002t0013g0048 a0001c0002t0013g0104 a0001c0002t0022g0101 others(9): Show |
15 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.*1+5107C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756205 | |||||||
chr3:119756232 | A | G | 1 | a0001c0002t0002g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.*1+5134A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756232 | |||||||
chr3:119756592 | A | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0118 others(12): Show |
17 | HG00423.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.*1+5494A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756592 | |||||||
chr3:119756707 | C | A | 1 | a0009c0026t0032g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.*1+5609C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756707 | |||||||
chr3:119756960 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.*1+5862C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119756960 | |||||||
chr3:119757050 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.*1+5952T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119757050 | |||||||
chr3:119757222 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*1+6124C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119757222 | |||||||
chr3:119757421 | A | T | 1 | a0001c0001t0027g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.*1+6323A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119757421 | |||||||
chr3:119757638 | C | T | 1 | a0001c0003t0018g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*1+6540C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119757638 | |||||||
chr3:119757752 | G | A | 1 | a0003c0027t0031g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.*1+6654G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119757752 | |||||||
chr3:119757870 | C | T | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.*1+6772C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119757870 | |||||||
chr3:119758060 | G | T | 89 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(86): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.*1+6962G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758060 | |||||||
chr3:119758088 | A | G | 1 | a0001c0003t0004g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*2-6964A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758088 | |||||||
chr3:119758093 | C | A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*2-6959C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758093 | |||||||
chr3:119758114 | A | G | 1 | a0001c0002t0006g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.*2-6938A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758114 | |||||||
chr3:119758201 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*2-6851A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758201 | |||||||
chr3:119758213 | C | T | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*2-6839C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758213 | |||||||
chr3:119758659 | C | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-6393C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758659 | |||||||
chr3:119758759 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.*2-6293A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758759 | |||||||
chr3:119758764 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.*2-6288G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119758764 | |||||||
chr3:119759251 | G | C | 90 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(87): Show |
99 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.*2-5801G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759251 | |||||||
chr3:119759504 | A | G | 1 | a0001c0003t0004g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*2-5548A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759504 | |||||||
chr3:119759594 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.*2-5458T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759594 | |||||||
chr3:119759612 | A | G | 90 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(87): Show |
99 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.*2-5440A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759612 | |||||||
chr3:119759619 | G | A | 1 | a0001c0003t0003g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*2-5433G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759619 | |||||||
chr3:119759689 | G | T | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*2-5363G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759689 | |||||||
chr3:119759703 | A | G | 1 | a0001c0001t0024g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.*2-5349A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759703 | |||||||
chr3:119759736 | G | A | 1 | a0001c0003t0003g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.*2-5316G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759736 | |||||||
chr3:119759916 | G | A | 136 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(133): Show |
151 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.*2-5136G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759916 | |||||||
chr3:119759923 | A | G | 2 | a0002c0004t0001g0337 a0002c0004t0001g0338 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*2-5129A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759923 | |||||||
chr3:119759933 | A | G | 1 | a0003c0005t0004g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*2-5119A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119759933 | |||||||
chr3:119760232 | G | A | 77 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(74): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.*2-4820G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119760232 | |||||||
chr3:119760404 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0235 |
2 | NA19060.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.*2-4648T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119760404 | |||||||
chr3:119760450 | T | A | 1 | a0001c0001t0001g0263 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*2-4602T>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119760450 | |||||||
chr3:119760915 | G | A | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.*2-4137G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119760915 | |||||||
chr3:119760963 | G | C | 11 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(8): Show |
12 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.*2-4089G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119760963 | |||||||
chr3:119761140 | C | A | 118 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(115): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.*2-3912C>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119761140 | |||||||
chr3:119761215 | A | G | 2 | a0009c0022t0005g0324 a0009c0026t0032g0099 |
2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.*2-3837A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119761215 | |||||||
chr3:119762002 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*2-3050A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762002 | |||||||
chr3:119762084 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.*2-2968G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762084 | |||||||
chr3:119762155 | A | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-2897A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762155 | |||||||
chr3:119762184 | A | G | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-2868A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762184 | |||||||
chr3:119762258 | ATACT | A | 136 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(133): Show |
151 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.*2-2787_*2-2784del others(4): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 119762258 | ||||||
chr3:119762508 | G | C | 2 | a0009c0022t0005g0324 a0009c0026t0032g0099 |
2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.*2-2544G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762508 | |||||||
chr3:119762555 | C | G | 1 | a0001c0002t0022g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*2-2497C>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762555 | |||||||
chr3:119762635 | G | A | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.*2-2417G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762635 | |||||||
chr3:119762754 | A | G | 5 | a0006c0010t0014g0034 a0006c0010t0014g0035 a0006c0010t0017g0031 others(2): Show |
5 | HG01891.hp1 HG06807.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2-2298A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762754 | |||||||
chr3:119762883 | A | C | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*2-2169A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762883 | |||||||
chr3:119762940 | A | C | 1 | a0006c0010t0033g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*2-2112A>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762940 | |||||||
chr3:119762997 | C | T | 2 | a0001c0003t0018g0332 a0001c0003t0018g0333 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.*2-2055C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119762997 | |||||||
chr3:119763149 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.*2-1903T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119763149 | |||||||
chr3:119763222 | G | A | 7 | a0001c0007t0008g0005 a0001c0007t0008g0006 a0001c0007t0008g0032 others(4): Show |
9 | HG01891.hp2 HG02602.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.*2-1830G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119763222 | |||||||
chr3:119763243 | G | A | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-1809G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119763243 | |||||||
chr3:119763425 | A | T | 2 | a0001c0014t0016g0109 a0001c0014t0016g0110 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.*2-1627A>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119763425 | |||||||
chr3:119763434 | A | G | 40 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0022 others(37): Show |
43 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.*2-1618A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119763434 | |||||||
chr3:119763463 | T | G | 1 | a0001c0002t0002g0061 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.*2-1589T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119763463 | |||||||
chr3:119763619 | T | TA | 11 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(8): Show |
12 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.*2-1422dupA | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 119763619 | ||||||
chr3:119763619 | TAAA | T | 6 | a0005c0008t0007g0004 a0005c0008t0007g0351 a0005c0008t0007g0352 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-1424_*2-1422del others(3): Show |
CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 119763619 | ||||||
chr3:119764004 | A | G | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*2-1048A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764004 | |||||||
chr3:119764014 | G | A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*2-1038G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764014 | |||||||
chr3:119764149 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG00621.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.*2-903G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764149 | |||||||
chr3:119764180 | C | T | 1 | a0004c0006t0001g0206 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.*2-872C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764180 | |||||||
chr3:119764215 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.*2-837T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764215 | |||||||
chr3:119764240 | A | G | 11 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(8): Show |
12 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.*2-812A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764240 | |||||||
chr3:119764375 | T | C | 1 | a0002c0004t0005g0345 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.*2-677T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764375 | |||||||
chr3:119764384 | T | G | 91 | a0001c0001t0003g0113 a0001c0001t0003g0116 a0001c0001t0003g0126 others(88): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.*2-668T>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764384 | |||||||
chr3:119764420 | G | A | 105 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(102): Show |
112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.*2-632G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764420 | |||||||
chr3:119764438 | C | T | 1 | a0002c0004t0001g0339 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.*2-614C>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764438 | |||||||
chr3:119764636 | T | C | 1 | a0006c0010t0033g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*2-416T>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764636 | |||||||
chr3:119764701 | G | C | 11 | a0002c0004t0005g0029 a0002c0004t0005g0335 a0002c0004t0005g0336 others(8): Show |
12 | HG00639.hp1 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.*2-351G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764701 | |||||||
chr3:119764708 | G | C | 1 | a0013c0020t0026g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*2-344G>C | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764708 | |||||||
chr3:119764723 | G | T | 1 | a0006c0010t0017g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*2-329G>T | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764723 | |||||||
chr3:119764817 | G | A | 1 | a0001c0001t0012g0288 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.*2-235G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764817 | |||||||
chr3:119764905 | A | G | 6 | a0001c0003t0003g0025 a0001c0003t0003g0027 a0001c0003t0003g0320 others(3): Show |
8 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.*2-147A>G | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764905 | |||||||
chr3:119764906 | G | A | 2 | a0001c0009t0005g0009 a0001c0009t0005g0105 |
3 | HG02280.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*2-146G>A | CFAP91 | ENSG00000183833.16 | transcript | ENST00000273390.9 | protein_coding | 17/17 | chr3 | 119764906 |