geneid | 402160 |
---|---|
ensemblid | ENSG00000206113.12 |
hgncid | 51180 |
symbol | CFAP99 |
name | cilia and flagella associated protein 99 |
refseq_nuc | NM_001193282.4 |
refseq_prot | NP_001180211.2 |
ensembl_nuc | ENST00000635017.2 |
ensembl_prot | ENSP00000488922.2 |
mane_status | MANE Select |
chr | chr4 |
start | 2418955 |
end | 2463002 |
strand | + |
ver | v1.2 |
region | chr4:2418955-2463002 |
region5000 | chr4:2413955-2468002 |
regionname0 | CFAP99_chr4_2418955_2463002 |
regionname5000 | CFAP99_chr4_2413955_2468002 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 646 | 194 | 75 | 25 | 59 | 13 | 21 | 47 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002 | 0/0 | 646 | 112 | 10 | 23 | 69 | 1 | 9 | 45 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0003 | 0/0 | 646 | 15 | 1 | 3 | 3 | 0 | 8 | 3 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0004 | 0/0 | 646 | 8 | 0 | 6 | 2 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0005 | 0/0 | 646 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0006 | 0/0 | 646 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0007 | 0/0 | 646 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0008 | 0/0 | 646 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0009 | 0/0 | 73 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0010 | 0/0 | 187 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0011 | 0/0 | 646 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0012 | 0/0 | 646 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0013 | 0/0 | 646 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0014 | 0/0 | 646 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0015 | 1/0 | 646 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0016 | 0/0 | 646 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0017 | 0/0 | 646 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1941 | 91 | 7 | 22 | 54 | 1 | 7 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0002 | 0/0 | 1941 | 71 | 24 | 8 | 26 | 4 | 9 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0003 | 0/0 | 1941 | 71 | 20 | 9 | 31 | 5 | 6 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0004 | 0/1 | 1941 | 23 | 11 | 4 | 0 | 4 | 3 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0005 | 0/0 | 1941 | 17 | 3 | 0 | 12 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0006 | 0/0 | 1941 | 15 | 12 | 3 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0007 | 0/0 | 1941 | 10 | 0 | 3 | 2 | 0 | 5 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0008 | 0/0 | 1941 | 8 | 0 | 6 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0009 | 0/0 | 1941 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0010 | 0/0 | 1941 | 3 | 1 | 0 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0011 | 0/0 | 1941 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0012 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0013 | 0/0 | 1941 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0014 | 0/0 | 1941 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0015 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0016 | 0/0 | 1941 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0017 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0018 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0019 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0020 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0021 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0022 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0023 | 1/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0024 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0025 | 0/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0026 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0027 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0028 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0029 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0030 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0031 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0032 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0033 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0034 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0035 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0036 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0037 | 0/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0038 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
c0039 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 233 | 334 | 81 | 59 | 138 | 14 | 40 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
t0002 | 0/0 | 233 | 12 | 11 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
t0003 | 0/0 | 233 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
t0004 | 0/0 | 233 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
t0005 | 0/0 | 233 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 1941 | 71 | 24 | 8 | 26 | 4 | 9 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0003 | 0/0 | 1941 | 71 | 20 | 9 | 31 | 5 | 6 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0004 | 0/1 | 1941 | 23 | 11 | 4 | 0 | 4 | 3 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0006 | 0/0 | 1941 | 15 | 12 | 3 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0012 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0013 | 0/0 | 1941 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0015 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0018 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0021 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0024 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0025 | 0/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0032 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0034 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0035 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0001 | 0/0 | 1941 | 91 | 7 | 22 | 54 | 1 | 7 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0005 | 0/0 | 1941 | 17 | 3 | 0 | 12 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0026 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0027 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0031 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0039 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0003c0007 | 0/0 | 1941 | 10 | 0 | 3 | 2 | 0 | 5 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0003c0010 | 0/0 | 1941 | 3 | 1 | 0 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0003c0016 | 0/0 | 1941 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0004c0008 | 0/0 | 1941 | 8 | 0 | 6 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0005c0009 | 0/0 | 1941 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0005c0017 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0006c0028 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0006c0029 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0007c0014 | 0/0 | 1941 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0008c0011 | 0/0 | 1941 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0009c0038 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0010c0033 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0011c0037 | 0/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0012c0030 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0013c0020 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0014c0022 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0015c0023 | 1/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0016c0036 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0017c0019 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 2173 | 69 | 22 | 8 | 26 | 4 | 9 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0002t0003 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0003t0001 | 0/0 | 2173 | 69 | 19 | 8 | 31 | 5 | 6 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0003t0002 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0003t0005 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0004t0001 | 0/1 | 2173 | 20 | 8 | 4 | 0 | 4 | 3 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0004t0002 | 0/0 | 2173 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0006t0001 | 0/0 | 2173 | 10 | 7 | 3 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0006t0002 | 0/0 | 2173 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0012t0001 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0013t0001 | 0/0 | 2173 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0015t0001 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0018t0001 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0021t0001 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0024t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0025t0001 | 0/0 | 2173 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0032t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0034t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0001c0035t0001 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0001t0001 | 0/0 | 2173 | 90 | 7 | 21 | 54 | 1 | 7 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0001t0004 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0005t0001 | 0/0 | 2173 | 15 | 1 | 0 | 12 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0005t0002 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0026t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0027t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0031t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0002c0039t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0003c0007t0001 | 0/0 | 2173 | 10 | 0 | 3 | 2 | 0 | 5 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0003c0010t0001 | 0/0 | 2173 | 3 | 1 | 0 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0003c0016t0001 | 0/0 | 2173 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0004c0008t0001 | 0/0 | 2173 | 8 | 0 | 6 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0005c0009t0001 | 0/0 | 2173 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0005c0017t0001 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0006c0028t0001 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0006c0029t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0007c0014t0001 | 0/0 | 2173 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0008c0011t0001 | 0/0 | 2173 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0009c0038t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0010c0033t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0011c0037t0001 | 0/0 | 2173 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0012c0030t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0013c0020t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0014c0022t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0015c0023t0001 | 1/0 | 2173 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0016c0036t0002 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
a0017c0019t0001 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | copy fasta | chr4 | 2413955 | 2468002 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0002t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0003t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0004t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0006t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0012t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0012t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0013t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0013t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0015t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0015t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0018t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0018t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0021t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0024t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0025t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0032t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0034t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0001c0035t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0005t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0026t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0027t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0031t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0002c0039t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0007t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0010t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0010t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0016t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0003c0016t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0004c0008t0001g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0004c0008t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0004c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0004c0008t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0004c0008t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0005c0009t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0005c0009t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0005c0009t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0005c0009t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0005c0017t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0005c0017t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0006c0028t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0006c0029t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0007c0014t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0007c0014t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0008c0011t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0008c0011t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0009c0038t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0010c0033t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0011c0037t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0012c0030t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0013c0020t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0014c0022t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0015c0023t0001g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0016c0036t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
a0017c0019t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0015 | EUR | GBR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0191 | EUR | GBR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0110 | EUR | FIN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00280 | hp2 | a0002 | c0001 | t0001 | g0254 | EUR | FIN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00408 | hp1 | a0001 | c0003 | t0001 | g0104 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00408 | hp2 | a0002 | c0027 | t0001 | g0278 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00438 | hp1 | a0002 | c0005 | t0001 | g0226 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00438 | hp2 | a0001 | c0032 | t0001 | g0261 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0279 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0233 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00597 | hp1 | a0002 | c0001 | t0001 | g0243 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00597 | hp2 | a0002 | c0005 | t0001 | g0277 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00609 | hp2 | a0002 | c0005 | t0001 | g0257 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00639 | hp1 | a0014 | c0022 | t0001 | g0196 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00642 | hp2 | a0002 | c0001 | t0001 | g0255 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00673 | hp2 | a0002 | c0001 | t0001 | g0291 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00735 | hp1 | a0002 | c0001 | t0001 | g0246 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00738 | hp1 | a0002 | c0001 | t0001 | g0235 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01069 | hp1 | a0002 | c0001 | t0001 | g0214 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01071 | hp2 | a0002 | c0001 | t0001 | g0017 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01074 | hp1 | a0003 | c0007 | t0001 | g0052 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01074 | hp2 | a0004 | c0008 | t0001 | g0249 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01081 | hp1 | a0002 | c0001 | t0001 | g0256 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01081 | hp2 | a0003 | c0007 | t0001 | g0117 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0316 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01106 | hp2 | a0001 | c0004 | t0001 | g0067 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0017 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01109 | hp2 | a0016 | c0036 | t0002 | g0035 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01167 | hp2 | a0001 | c0006 | t0001 | g0165 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0121 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01169 | hp2 | a0002 | c0001 | t0001 | g0228 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0236 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01243 | hp1 | a0006 | c0029 | t0001 | g0171 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0098 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0180 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01255 | hp2 | a0001 | c0003 | t0005 | g0313 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01256 | hp1 | a0002 | c0001 | t0001 | g0301 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01257 | hp2 | a0004 | c0008 | t0001 | g0217 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01258 | hp2 | a0004 | c0008 | t0001 | g0003 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01261 | hp1 | a0008 | c0011 | t0001 | g0091 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0198 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01358 | hp1 | a0002 | c0001 | t0004 | g0224 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0169 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01496 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0218 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0152 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0014 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0153 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0209 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0041 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0014 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0315 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01884 | hp2 | a0001 | c0006 | t0001 | g0099 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01891 | hp1 | a0002 | c0005 | t0002 | g0036 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01928 | hp1 | a0004 | c0008 | t0001 | g0266 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01928 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01934 | hp1 | a0004 | c0008 | t0001 | g0003 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01934 | hp2 | a0001 | c0004 | t0001 | g0203 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01975 | hp2 | a0001 | c0006 | t0001 | g0168 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01978 | hp1 | a0003 | c0007 | t0001 | g0123 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01978 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0275 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG01981 | hp2 | a0010 | c0033 | t0001 | g0200 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02004 | hp1 | a0002 | c0026 | t0001 | g0020 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02004 | hp2 | a0001 | c0034 | t0001 | g0187 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0281 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02055 | hp1 | a0005 | c0017 | t0001 | g0166 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0242 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0286 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0227 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02080 | hp2 | a0002 | c0005 | t0001 | g0102 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02083 | hp1 | a0002 | c0031 | t0001 | g0294 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0085 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02129 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0258 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02135 | hp2 | a0002 | c0001 | t0001 | g0225 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02145 | hp2 | a0001 | c0012 | t0001 | g0084 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02148 | hp1 | a0004 | c0008 | t0001 | g0003 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0245 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02155 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0061 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0271 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02257 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02257 | hp2 | a0001 | c0006 | t0002 | g0042 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02280 | hp2 | a0002 | c0005 | t0002 | g0037 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0222 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02523 | hp1 | a0002 | c0001 | t0001 | g0282 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02523 | hp2 | a0001 | c0024 | t0001 | g0185 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02572 | hp2 | a0001 | c0015 | t0001 | g0012 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0155 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02602 | hp2 | a0008 | c0011 | t0001 | g0090 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02615 | hp1 | a0005 | c0009 | t0001 | g0156 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02615 | hp2 | a0001 | c0006 | t0001 | g0128 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02622 | hp2 | a0005 | c0009 | t0001 | g0159 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0086 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02647 | hp2 | a0001 | c0015 | t0001 | g0285 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0183 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02683 | hp2 | a0003 | c0010 | t0001 | g0069 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02698 | hp1 | a0003 | c0007 | t0001 | g0268 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02698 | hp2 | a0002 | c0005 | t0001 | g0007 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02717 | hp1 | a0001 | c0004 | t0001 | g0302 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02723 | hp1 | a0005 | c0009 | t0001 | g0160 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0305 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02735 | hp1 | a0002 | c0001 | t0001 | g0216 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02738 | hp1 | a0003 | c0007 | t0001 | g0250 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0050 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02886 | hp2 | a0002 | c0001 | t0001 | g0284 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02895 | hp1 | a0003 | c0010 | t0001 | g0080 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02895 | hp2 | a0001 | c0006 | t0001 | g0029 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0306 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02896 | hp2 | a0001 | c0006 | t0002 | g0040 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02897 | hp1 | a0001 | c0006 | t0001 | g0031 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0312 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0310 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02970 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02976 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0293 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0215 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0174 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03098 | hp1 | a0001 | c0006 | t0002 | g0038 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03139 | hp1 | a0001 | c0035 | t0001 | g0030 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0012 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03209 | hp1 | a0001 | c0018 | t0001 | g0162 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03209 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03225 | hp1 | a0001 | c0004 | t0002 | g0043 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0234 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03453 | hp1 | a0005 | c0009 | t0001 | g0158 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03453 | hp2 | a0002 | c0001 | t0001 | g0290 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03486 | hp1 | a0002 | c0001 | t0001 | g0283 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0089 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03491 | hp1 | a0001 | c0013 | t0001 | g0046 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03492 | hp2 | a0002 | c0001 | t0001 | g0272 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03516 | hp1 | a0001 | c0006 | t0002 | g0034 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03516 | hp2 | a0001 | c0006 | t0001 | g0164 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03540 | hp1 | a0001 | c0004 | t0002 | g0045 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03540 | hp2 | a0005 | c0017 | t0001 | g0157 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0206 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0311 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03654 | hp1 | a0003 | c0007 | t0001 | g0071 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03669 | hp1 | a0003 | c0016 | t0001 | g0068 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03669 | hp2 | a0002 | c0001 | t0001 | g0273 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03688 | hp1 | a0003 | c0007 | t0001 | g0259 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03704 | hp2 | a0001 | c0013 | t0001 | g0115 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0267 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03710 | hp2 | a0001 | c0025 | t0001 | g0269 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03834 | hp1 | a0002 | c0005 | t0001 | g0105 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0193 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03927 | hp1 | a0001 | c0004 | t0001 | g0188 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03927 | hp2 | a0011 | c0037 | t0001 | g0280 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG04184 | hp1 | a0001 | c0004 | t0001 | g0063 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG04184 | hp2 | a0001 | c0004 | t0001 | g0213 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0184 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG04199 | hp2 | a0003 | c0016 | t0001 | g0059 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0190 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG04228 | hp2 | a0003 | c0007 | t0001 | g0260 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18522 | hp1 | a0001 | c0018 | t0001 | g0130 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18522 | hp2 | a0001 | c0004 | t0002 | g0044 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18906 | hp2 | a0001 | c0006 | t0002 | g0173 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18943 | hp2 | a0007 | c0014 | t0001 | g0262 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18944 | hp1 | a0002 | c0001 | t0001 | g0304 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18944 | hp2 | a0002 | c0001 | t0001 | g0296 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18947 | hp1 | a0002 | c0005 | t0001 | g0300 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18948 | hp2 | a0002 | c0001 | t0001 | g0265 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18950 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18951 | hp2 | a0004 | c0008 | t0001 | g0229 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18953 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18953 | hp2 | a0003 | c0007 | t0001 | g0297 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18957 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18961 | hp1 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18963 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18963 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18964 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18964 | hp2 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18968 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18970 | hp1 | a0002 | c0001 | t0001 | g0241 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0264 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18974 | hp1 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18975 | hp1 | a0009 | c0038 | t0001 | g0292 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18975 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18977 | hp1 | a0002 | c0005 | t0001 | g0274 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18977 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18983 | hp2 | a0004 | c0008 | t0001 | g0003 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18984 | hp1 | a0003 | c0007 | t0001 | g0065 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18984 | hp2 | a0012 | c0030 | t0001 | g0149 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18990 | hp2 | a0002 | c0005 | t0001 | g0244 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18995 | hp1 | a0002 | c0001 | t0001 | g0295 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18995 | hp2 | a0013 | c0020 | t0001 | g0073 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18997 | hp1 | a0002 | c0005 | t0001 | g0276 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18997 | hp2 | a0007 | c0014 | t0001 | g0113 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0270 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19007 | hp2 | a0002 | c0039 | t0001 | g0001 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19009 | hp1 | a0002 | c0005 | t0001 | g0103 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19010 | hp2 | a0002 | c0005 | t0001 | g0263 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0127 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19030 | hp2 | a0006 | c0028 | t0001 | g0170 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19043 | hp1 | a0002 | c0005 | t0001 | g0048 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0178 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19056 | hp2 | a0002 | c0005 | t0001 | g0116 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19060 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19063 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19063 | hp2 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19066 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19074 | hp1 | a0003 | c0010 | t0001 | g0064 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19075 | hp1 | a0002 | c0001 | t0001 | g0299 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19084 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19087 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19088 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19089 | hp2 | a0002 | c0005 | t0001 | g0163 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0232 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19090 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA19091 | hp2 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA20129 | hp1 | a0017 | c0019 | t0001 | g0230 | AFR | ASW | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ASW | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA20752 | hp1 | a0001 | c0004 | t0001 | g0204 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0195 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0150 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA20805 | hp2 | a0001 | c0004 | t0001 | g0202 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02109 | hp1 | a0001 | c0004 | t0001 | g0303 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02486 | hp1 | a0001 | c0021 | t0001 | g0308 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0309 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03471 | hp1 | a0001 | c0006 | t0001 | g0167 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG06807 | hp1 | a0001 | c0012 | t0001 | g0083 | AFR | USA | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | USA | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA21309 | hp1 | a0002 | c0001 | t0001 | g0175 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0001 | g0212 | REF | REF | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
homoSapiens_grch38 | hp1 | a0015 | c0023 | t0001 | g0201 | REF | REF | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2436977
|
A | G | 1 | a0005 | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
missense_variant | MODERATE | c.215A>G | p.Asp72Gly | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/16 | 371/2173 | 215/1941 | 72/646 | chr4 | 2436977 | ||
chr4:2436982
|
C | T | 1 | a0009 | 1 | NA18975.hp1 | stop_gained | HIGH | c.220C>T | p.Arg74* | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/16 | 376/2173 | 220/1941 | 74/646 | chr4 | 2436982 | ||
chr4:2445166
|
T | C | 1 | a0017 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.500T>C | p.Leu167Pro | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/16 | 656/2173 | 500/1941 | 167/646 | chr4 | 2445166 | ||
chr4:2445228
|
A | T | 1 | a0010 | 1 | HG01981.hp2 | stop_gained | HIGH | c.562A>T | p.Lys188* | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/16 | 718/2173 | 562/1941 | 188/646 | chr4 | 2445228 | ||
chr4:2449967
|
C | T | 3 | a0003a0010a0011 | 17 | HG01074.hp1 HG01081.hp2 HG01978.hp1 others(14): Show |
missense_variant | MODERATE | c.757C>T | p.Arg253Cys | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/16 | 913/2173 | 757/1941 | 253/646 | chr4 | 2449967 | ||
chr4:2450973
|
G | T | 1 | a0012 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.822G>T | p.Gln274His | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/16 | 978/2173 | 822/1941 | 274/646 | chr4 | 2450973 | ||
chr4:2452155
|
G | A | 1 | a0013 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.970G>A | p.Val324Met | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/16 | 1126/2173 | 970/1941 | 324/646 | chr4 | 2452155 | ||
chr4:2458756
|
C | T | 1 | a0016 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1195C>T | p.Arg399Trp | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1351/2173 | 1195/1941 | 399/646 | chr4 | 2458756 | ||
chr4:2458792
|
G | C | 1 | a0008 | 2 | HG01261.hp1 HG02602.hp2 |
missense_variant | MODERATE | c.1231G>C | p.Glu411Gln | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1387/2173 | 1231/1941 | 411/646 | chr4 | 2458792 | ||
chr4:2458819
|
G | A | 1 | a0004 | 8 | HG01074.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
missense_variant | MODERATE | c.1258G>A | p.Ala420Thr | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1414/2173 | 1258/1941 | 420/646 | chr4 | 2458819 | ||
chr4:2458835
|
C | T | 1 | a0006 | 2 | HG01243.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.1274C>T | p.Thr425Met | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1430/2173 | 1274/1941 | 425/646 | chr4 | 2458835 | ||
chr4:2458844
|
C | T | 4 | a0002a0009a0011others(1): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
missense_variant | MODERATE | c.1283C>T | p.Ala428Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1439/2173 | 1283/1941 | 428/646 | chr4 | 2458844 | ||
chr4:2460115
|
C | T | 1 | a0016 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1534C>T | p.Arg512Trp | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/16 | 1690/2173 | 1534/1941 | 512/646 | chr4 | 2460115 | ||
chr4:2460119
|
G | A | 1 | a0014 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1538G>A | p.Arg513His | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/16 | 1694/2173 | 1538/1941 | 513/646 | chr4 | 2460119 | ||
chr4:2460161
|
A | G | 16 | a0001a0002a0003others(13): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
missense_variant | MODERATE | c.1580A>G | p.His527Arg | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/16 | 1736/2173 | 1580/1941 | 527/646 | chr4 | 2460161 | ||
chr4:2462501
|
G | C | 1 | a0007 | 2 | NA18943.hp2 NA18997.hp2 |
missense_variant | MODERATE | c.1720G>C | p.Val574Leu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/16 | 1876/2173 | 1720/1941 | 574/646 | chr4 | 2462501 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2426574
|
C | T | 1 | a0002c0039 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.99C>T | p.Ala33Ala | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/16 | 255/2173 | 99/1941 | 33/646 | chr4 | 2426574 | ||
chr4:2436951
|
C | T | 1 | a0001c0018 | 2 | HG03209.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.189C>T | p.Val63Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/16 | 345/2173 | 189/1941 | 63/646 | chr4 | 2436951 | ||
chr4:2443204
|
A | G | 11 | a0001c0004a0001c0006a0001c0015others(8): Show | 61 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(58): Show |
synonymous_variant | LOW | c.426A>G | p.Pro142Pro | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/16 | 582/2173 | 426/1941 | 142/646 | chr4 | 2443204 | ||
chr4:2445290
|
C | T | 1 | a0001c0032 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.624C>T | p.Val208Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/16 | 780/2173 | 624/1941 | 208/646 | chr4 | 2445290 | ||
chr4:2449963
|
A | G | 1 | a0002c0031 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.753A>G | p.Glu251Glu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/16 | 909/2173 | 753/1941 | 251/646 | chr4 | 2449963 | ||
chr4:2452298
|
G | A | 1 | a0001c0021 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1113G>A | p.Gln371Gln | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/16 | 1269/2173 | 1113/1941 | 371/646 | chr4 | 2452298 | ||
chr4:2459120
|
C | T | 2 | a0001c0025a0001c0035 | 2 | HG03139.hp1 HG03710.hp2 |
synonymous_variant | LOW | c.1317C>T | p.Ile439Ile | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/16 | 1473/2173 | 1317/1941 | 439/646 | chr4 | 2459120 | ||
chr4:2459222
|
G | A | 1 | a0001c0012 | 2 | HG02145.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.1419G>A | p.Gln473Gln | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/16 | 1575/2173 | 1419/1941 | 473/646 | chr4 | 2459222 | ||
chr4:2459228
|
G | A | 5 | a0001c0013a0001c0034a0002c0026others(2): Show | 17 | HG01074.hp1 HG01081.hp2 HG01978.hp1 others(14): Show |
synonymous_variant | LOW | c.1425G>A | p.Thr475Thr | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/16 | 1581/2173 | 1425/1941 | 475/646 | chr4 | 2459228 | ||
chr4:2462452
|
A | G | 24 | a0001c0003a0001c0004a0001c0012others(21): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
synonymous_variant | LOW | c.1671A>G | p.Glu557Glu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/16 | 1827/2173 | 1671/1941 | 557/646 | chr4 | 2462452 | ||
chr4:2462572
|
G | T | 1 | a0001c0024 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1791G>T | p.Val597Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/16 | 1947/2173 | 1791/1941 | 597/646 | chr4 | 2462572 | ||
chr4:2462818
|
A | G | 1 | a0002c0027 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.1833A>G | p.Leu611Leu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 16/16 | 1989/2173 | 1833/1941 | 611/646 | chr4 | 2462818 | ||
chr4:2462842
|
G | A | 1 | a0001c0015 | 2 | HG02572.hp2 HG02647.hp2 |
synonymous_variant | LOW | c.1857G>A | p.Leu619Leu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 16/16 | 2013/2173 | 1857/1941 | 619/646 | chr4 | 2462842 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2418971
|
G | A | 1 | a0002c0001t0004 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/16 | 7505 | chr4 | 2418971 | |||||
chr4:2419004
|
G | A | 5 | a0001c0003t0002a0001c0004t0002a0001c0006t0002others(2): Show | 12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-107G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/16 | 7472 | chr4 | 2419004 | |||||
chr4:2419005
|
C | A | 1 | a0001c0002t0003 | 2 | HG02896.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-106C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/16 | 7471 | chr4 | 2419005 | |||||
chr4:2462970
|
A | C | 1 | a0001c0003t0005 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*44A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 16/16 | 44 | chr4 | 2462970 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2419112
|
T | A | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+19T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419112 | ||||||
chr4:2419170
|
G | C | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+77G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419170 | ||||||
chr4:2419195
|
T | A | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+102T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419195 | ||||||
chr4:2419197
|
T | C | 6 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(3): Show | 7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+104T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419197 | ||||||
chr4:2419240
|
CT | C | 18 | a0001c0002t0001g0033a0001c0002t0001g0049a0001c0003t0001g0032others(15): Show | 18 | HG01109.hp2 HG01517.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18+160delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2419240 | |||||
chr4:2419262
|
A | G | 1 | a0001c0004t0001g0316 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18+169A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419262 | ||||||
chr4:2419264
|
T | C | 1 | a0001c0003t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-18+171T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419264 | ||||||
chr4:2419295
|
C | A | 1 | a0001c0002t0001g0051 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-18+202C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419295 | ||||||
chr4:2419314
|
C | T | 1 | a0001c0003t0001g0315 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-18+221C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419314 | ||||||
chr4:2419402
|
G | A | 85 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(82): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-18+309G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419402 | ||||||
chr4:2419834
|
G | A | 5 | a0001c0003t0001g0016a0001c0003t0001g0126a0001c0003t0001g0127others(2): Show | 6 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+741G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419834 | ||||||
chr4:2419841
|
T | C | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+748T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419841 | ||||||
chr4:2419987
|
C | G | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+894C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419987 | ||||||
chr4:2420072
|
A | T | 1 | a0002c0001t0001g0304 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-18+979A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420072 | ||||||
chr4:2420184
|
T | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+1091T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420184 | ||||||
chr4:2420238
|
G | A | 2 | a0001c0006t0002g0034a0001c0006t0002g0173 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+1145G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420238 | ||||||
chr4:2420488
|
C | T | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+1395C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420488 | ||||||
chr4:2420546
|
C | T | 87 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(84): Show | 93 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-18+1453C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420546 | ||||||
chr4:2420753
|
C | G | 1 | a0002c0001t0001g0125 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-18+1660C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420753 | ||||||
chr4:2420756
|
TA | T | 10 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(7): Show | 11 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+1666delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2420756 | |||||
chr4:2420817
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+1724C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420817 | ||||||
chr4:2420904
|
T | C | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+1811T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420904 | ||||||
chr4:2421006
|
T | A | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+1913T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421006 | ||||||
chr4:2421082
|
A | G | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+1989A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421082 | ||||||
chr4:2421099
|
C | T | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+2006C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421099 | ||||||
chr4:2421121
|
A | C | 1 | a0002c0001t0001g0301 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-18+2028A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421121 | ||||||
chr4:2421181
|
G | C | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+2088G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421181 | ||||||
chr4:2421349
|
C | A | 1 | a0001c0018t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+2256C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421349 | ||||||
chr4:2421350
|
C | CT | 14 | a0001c0002t0001g0053a0001c0002t0001g0055a0001c0002t0001g0056others(11): Show | 14 | HG01074.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+2279dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | |||||
chr4:2421350
|
C | CTT | 122 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0033others(119): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-18+2278_-18+2279d others(4): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | |||||
chr4:2421350
|
C | CTTT | 102 | a0001c0002t0001g0018a0001c0002t0001g0118a0001c0002t0001g0219others(99): Show | 118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-18+2277_-18+2279d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | |||||
chr4:2421350
|
C | CTTTT | 18 | a0001c0002t0001g0298a0001c0003t0001g0024a0001c0003t0001g0025others(15): Show | 20 | HG00735.hp2 HG01071.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+2276_-18+2279d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | |||||
chr4:2421377
|
T | G | 1 | a0016c0036t0002g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+2284T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421377 | ||||||
chr4:2421447
|
C | T | 6 | a0001c0003t0001g0016a0001c0003t0001g0126a0001c0003t0001g0127others(3): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+2354C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421447 | ||||||
chr4:2421496
|
G | A | 4 | a0001c0003t0001g0218a0002c0001t0001g0002a0002c0001t0001g0017others(1): Show | 8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+2403G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421496 | ||||||
chr4:2421608
|
C | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+2515C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421608 | ||||||
chr4:2421639
|
G | A | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+2546G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421639 | ||||||
chr4:2421725
|
GA | G | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+2639delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421725 | |||||
chr4:2421879
|
C | CA | 25 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0016others(22): Show | 27 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-18+2802dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421879 | |||||
chr4:2421879
|
C | CAA | 31 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(28): Show | 31 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18+2801_-18+2802d others(4): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421879 | |||||
chr4:2421879
|
CA | C | 15 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(12): Show | 17 | HG01255.hp2 HG01256.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+2802delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421879 | |||||
chr4:2421950
|
C | T | 1 | a0001c0004t0001g0212 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-18+2857C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421950 | ||||||
chr4:2421978
|
G | A | 18 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(15): Show | 19 | HG01243.hp1 HG01884.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+2885G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421978 | ||||||
chr4:2422373
|
C | T | 105 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(102): Show | 123 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-18+3280C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422373 | ||||||
chr4:2422433
|
G | A | 5 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(2): Show | 6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+3340G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422433 | ||||||
chr4:2422470
|
C | G | 268 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(265): Show | 296 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-18+3377C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422470 | ||||||
chr4:2422648
|
T | C | 110 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(107): Show | 128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-18+3555T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422648 | ||||||
chr4:2422711
|
G | T | 6 | a0005c0009t0001g0156a0005c0009t0001g0158a0005c0009t0001g0159others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+3618G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422711 | ||||||
chr4:2422755
|
G | A | 3 | a0001c0003t0001g0131a0001c0003t0001g0132a0001c0003t0001g0133 | 3 | NA18939.hp1 NA19079.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-18+3662G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422755 | ||||||
chr4:2422839
|
A | G | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-17-3620A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422839 | ||||||
chr4:2422930
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17-3529C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422930 | ||||||
chr4:2422930
|
C | T | 1 | a0002c0001t0001g0017 | 2 | HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-17-3529C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422930 | ||||||
chr4:2423007
|
G | A | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-3452G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423007 | ||||||
chr4:2423257
|
C | T | 2 | a0001c0004t0001g0041a0001c0004t0001g0209 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-17-3202C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423257 | ||||||
chr4:2423324
|
C | T | 89 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(86): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-3135C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423324 | ||||||
chr4:2423541
|
T | G | 1 | a0002c0001t0001g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-17-2918T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423541 | ||||||
chr4:2423753
|
C | T | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-2706C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423753 | ||||||
chr4:2423754
|
G | C | 5 | a0001c0003t0001g0016a0001c0003t0001g0126a0001c0003t0001g0127others(2): Show | 6 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-2705G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423754 | ||||||
chr4:2423832
|
C | T | 107 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(104): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-17-2627C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423832 | ||||||
chr4:2423841
|
G | A | 1 | a0002c0001t0001g0223 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-17-2618G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423841 | ||||||
chr4:2423842
|
C | G | 269 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(266): Show | 297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-17-2617C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423842 | ||||||
chr4:2423907
|
C | T | 3 | a0001c0002t0001g0207a0001c0004t0001g0206a0001c0035t0001g0030 | 3 | HG02559.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17-2552C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423907 | ||||||
chr4:2423967
|
G | A | 2 | a0005c0009t0001g0156a0005c0017t0001g0166 | 2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-17-2492G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423967 | ||||||
chr4:2424013
|
G | A | 1 | a0002c0001t0001g0005 | 3 | NA18967.hp1 NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-17-2446G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424013 | ||||||
chr4:2424228
|
G | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-2231G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424228 | ||||||
chr4:2424254
|
C | T | 7 | a0001c0002t0001g0150a0001c0002t0001g0151a0001c0002t0001g0152others(4): Show | 7 | HG01358.hp2 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-2205C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424254 | ||||||
chr4:2424294
|
A | G | 1 | a0001c0003t0001g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-17-2165A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424294 | ||||||
chr4:2424418
|
A | G | 10 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(7): Show | 10 | HG01109.hp2 HG02257.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-2041A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424418 | ||||||
chr4:2424461
|
G | C | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-1998G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424461 | ||||||
chr4:2424480
|
A | G | 105 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(102): Show | 123 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-17-1979A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424480 | ||||||
chr4:2424503
|
C | T | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-1956C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424503 | ||||||
chr4:2424555
|
T | G | 163 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0022others(160): Show | 173 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-17-1904T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424555 | ||||||
chr4:2424578
|
T | C | 4 | a0001c0003t0001g0218a0002c0001t0001g0002a0002c0001t0001g0017others(1): Show | 8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-1881T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424578 | ||||||
chr4:2424615
|
G | T | 1 | a0002c0005t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-1844G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424615 | ||||||
chr4:2424727
|
C | T | 2 | a0002c0005t0002g0036a0002c0005t0002g0037 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-17-1732C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424727 | ||||||
chr4:2424730
|
C | T | 105 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(102): Show | 123 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-17-1729C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424730 | ||||||
chr4:2424806
|
C | T | 5 | a0001c0003t0001g0016a0001c0003t0001g0126a0001c0003t0001g0127others(2): Show | 6 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-1653C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424806 | ||||||
chr4:2424811
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-1648C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424811 | ||||||
chr4:2424884
|
G | A | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-1575G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424884 | ||||||
chr4:2424915
|
C | T | 89 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(86): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-1544C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424915 | ||||||
chr4:2425127
|
C | A | 1 | a0001c0002t0001g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-17-1332C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425127 | ||||||
chr4:2425167
|
T | C | 1 | a0002c0001t0001g0135 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-17-1292T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425167 | ||||||
chr4:2425193
|
G | C | 1 | a0003c0016t0001g0059 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-17-1266G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425193 | ||||||
chr4:2425381
|
T | C | 282 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(279): Show | 310 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.-17-1078T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425381 | ||||||
chr4:2425400
|
C | T | 6 | a0005c0009t0001g0156a0005c0009t0001g0158a0005c0009t0001g0159others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-1059C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425400 | ||||||
chr4:2425478
|
T | G | 37 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(34): Show | 37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.-17-981T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425478 | ||||||
chr4:2425553
|
T | C | 50 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(47): Show | 51 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17-906T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425553 | ||||||
chr4:2425663
|
C | A | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0307others(10): Show | 15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-796C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425663 | ||||||
chr4:2425672
|
G | A | 1 | a0001c0006t0002g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-17-787G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425672 | ||||||
chr4:2425781
|
C | A | 47 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(44): Show | 48 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-17-678C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425781 | ||||||
chr4:2425784
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17-675A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425784 | ||||||
chr4:2425917
|
G | A | 39 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(36): Show | 42 | HG00673.hp1 HG01074.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-17-542G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425917 | ||||||
chr4:2425929
|
G | C | 33 | a0001c0002t0001g0033a0001c0002t0001g0137a0001c0002t0001g0142others(30): Show | 33 | HG00609.hp1 HG00621.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-530G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425929 | ||||||
chr4:2425953
|
A | G | 1 | a0002c0001t0001g0291 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-17-506A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425953 | ||||||
chr4:2426000
|
C | A | 10 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0023others(7): Show | 11 | HG01069.hp2 HG01071.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-459C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426000 | ||||||
chr4:2426024
|
C | G | 2 | a0005c0009t0001g0159a0005c0009t0001g0160 | 2 | HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-17-435C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426024 | ||||||
chr4:2426172
|
G | A | 103 | a0001c0002t0001g0018a0001c0002t0001g0298a0001c0003t0001g0019others(100): Show | 121 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-17-287G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426172 | ||||||
chr4:2426258
|
T | C | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-17-201T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426258 | ||||||
chr4:2426295
|
C | T | 5 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(2): Show | 6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-164C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426295 | ||||||
chr4:2426306
|
T | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-153T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426306 | ||||||
chr4:2426308
|
T | G | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-151T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426308 | ||||||
chr4:2426309
|
AGGCCC | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-146_-17-142del others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2426309 | |||||
chr4:2426367
|
C | T | 49 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(46): Show | 50 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-17-92C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426367 | ||||||
chr4:2426409
|
G | A | 1 | a0002c0001t0004g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-17-50G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426409 | ||||||
chr4:2426663
|
A | ATGCCTTC others(8): Show |
6 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(3): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+87_111+101dupA others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2426663 | |||||
chr4:2426736
|
G | A | 108 | a0001c0002t0001g0018a0001c0002t0001g0176a0001c0002t0001g0177others(105): Show | 126 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.111+150G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426736 | ||||||
chr4:2426805
|
G | A | 1 | a0001c0004t0001g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.111+219G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426805 | ||||||
chr4:2426810
|
C | T | 2 | a0001c0004t0001g0302a0001c0004t0001g0303 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.111+224C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426810 | ||||||
chr4:2426847
|
C | G | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+261C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426847 | ||||||
chr4:2426877
|
C | T | 1 | a0005c0017t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111+291C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426877 | ||||||
chr4:2427008
|
G | A | 1 | a0002c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.111+422G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427008 | ||||||
chr4:2427074
|
G | A | 1 | a0016c0036t0002g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+488G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427074 | ||||||
chr4:2427182
|
C | A | 89 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(86): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.111+596C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427182 | ||||||
chr4:2427231
|
C | G | 1 | a0001c0003t0001g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.111+645C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427231 | ||||||
chr4:2427258
|
T | G | 12 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+672T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427258 | ||||||
chr4:2427283
|
T | C | 1 | a0002c0001t0001g0225 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111+697T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427283 | ||||||
chr4:2427291
|
C | T | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+705C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427291 | ||||||
chr4:2427295
|
A | C | 113 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(110): Show | 122 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.111+709A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427295 | ||||||
chr4:2427340
|
T | C | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+754T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427340 | ||||||
chr4:2427378
|
A | G | 11 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0023others(8): Show | 13 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+792A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427378 | ||||||
chr4:2427401
|
T | C | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+815T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427401 | ||||||
chr4:2427474
|
A | C | 113 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(110): Show | 133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.111+888A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427474 | ||||||
chr4:2427559
|
G | A | 1 | a0006c0028t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.111+973G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427559 | ||||||
chr4:2427601
|
G | A | 89 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(86): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.111+1015G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427601 | ||||||
chr4:2427621
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0057 | 3 | HG02135.hp1 NA18948.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.111+1035C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427621 | ||||||
chr4:2427643
|
T | C | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+1057T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427643 | ||||||
chr4:2427691
|
A | G | 6 | a0005c0009t0001g0156a0005c0009t0001g0158a0005c0009t0001g0159others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1105A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427691 | ||||||
chr4:2427728
|
G | A | 202 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0051others(199): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.111+1142G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427728 | ||||||
chr4:2427750
|
A | C | 57 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(54): Show | 60 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.111+1164A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427750 | ||||||
chr4:2427887
|
C | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+1301C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427887 | ||||||
chr4:2427907
|
C | G | 6 | a0005c0009t0001g0156a0005c0009t0001g0158a0005c0009t0001g0159others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1321C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427907 | ||||||
chr4:2427927
|
G | A | 6 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(3): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+1341G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427927 | ||||||
chr4:2427968
|
G | A | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1382G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427968 | ||||||
chr4:2427974
|
G | A | 1 | a0001c0004t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.111+1388G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427974 | ||||||
chr4:2427996
|
G | A | 6 | a0005c0009t0001g0156a0005c0009t0001g0158a0005c0009t0001g0159others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1410G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427996 | ||||||
chr4:2428021
|
CA | C | 6 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(3): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+1436delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428021 | ||||||
chr4:2428155
|
G | A | 9 | a0001c0002t0001g0179a0001c0002t0001g0182a0001c0002t0001g0208others(6): Show | 9 | HG01255.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+1569G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428155 | ||||||
chr4:2428233
|
G | A | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+1647G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428233 | ||||||
chr4:2428432
|
C | A | 1 | a0001c0002t0001g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.111+1846C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428432 | ||||||
chr4:2428434
|
G | A | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1848G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428434 | ||||||
chr4:2428442
|
C | G | 1 | a0001c0006t0002g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111+1856C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428442 | ||||||
chr4:2428508
|
A | G | 176 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(173): Show | 197 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.111+1922A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428508 | ||||||
chr4:2428548
|
G | A | 31 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(28): Show | 31 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.111+1962G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428548 | ||||||
chr4:2428566
|
G | A | 1 | a0002c0005t0001g0226 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.111+1980G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428566 | ||||||
chr4:2428571
|
C | T | 270 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(267): Show | 297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.111+1985C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428571 | ||||||
chr4:2428716
|
G | A | 2 | a0001c0003t0001g0293a0002c0001t0001g0008 | 4 | HG02257.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+2130G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428716 | ||||||
chr4:2428819
|
TCCTC | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+2239_111+2242d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2428819 | |||||
chr4:2428898
|
G | A | 1 | a0001c0003t0001g0060 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.111+2312G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428898 | ||||||
chr4:2428960
|
C | G | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.111+2374C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428960 | ||||||
chr4:2428971
|
C | T | 1 | a0001c0004t0001g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.111+2385C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428971 | ||||||
chr4:2428977
|
G | A | 2 | a0001c0003t0001g0293a0002c0001t0001g0008 | 4 | HG02257.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+2391G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428977 | ||||||
chr4:2429094
|
C | T | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+2508C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429094 | ||||||
chr4:2429131
|
C | T | 1 | a0001c0004t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.111+2545C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429131 | ||||||
chr4:2429160
|
A | C | 233 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(230): Show | 261 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.111+2574A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429160 | ||||||
chr4:2429184
|
C | A | 1 | a0002c0001t0001g0225 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111+2598C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429184 | ||||||
chr4:2429198
|
G | A | 1 | a0002c0001t0001g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.111+2612G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429198 | ||||||
chr4:2429241
|
C | T | 1 | a0001c0003t0001g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.111+2655C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429241 | ||||||
chr4:2429300
|
C | CA | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+2722dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429300 | |||||
chr4:2429319
|
A | G | 1 | a0001c0003t0001g0133 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.111+2733A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429319 | ||||||
chr4:2429338
|
G | C | 91 | a0001c0002t0001g0018a0001c0002t0001g0298a0001c0003t0001g0019others(88): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.111+2752G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429338 | ||||||
chr4:2429339
|
G | A | 12 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+2753G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429339 | ||||||
chr4:2429462
|
G | A | 1 | a0002c0001t0001g0228 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.111+2876G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429462 | ||||||
chr4:2429593
|
C | CT | 11 | a0001c0004t0001g0202a0001c0004t0001g0203a0001c0004t0002g0043others(8): Show | 11 | HG01109.hp2 HG01934.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+3023dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | |||||
chr4:2429593
|
CT | C | 20 | a0001c0002t0001g0004a0001c0002t0001g0176a0001c0003t0001g0004others(17): Show | 21 | HG01243.hp1 HG01256.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.111+3023delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | |||||
chr4:2429593
|
CTT | C | 245 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0022others(242): Show | 272 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.111+3022_111+3023d others(4): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | |||||
chr4:2429593
|
CTTT | C | 7 | a0001c0002t0001g0062a0001c0002t0001g0307a0001c0003t0001g0087others(4): Show | 7 | HG02155.hp2 HG03041.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+3021_111+3023d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | |||||
chr4:2429599
|
T | C | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+3013T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429599 | ||||||
chr4:2429677
|
C | T | 12 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+3091C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429677 | ||||||
chr4:2429853
|
G | A | 283 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(280): Show | 311 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.111+3267G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429853 | ||||||
chr4:2429917
|
A | C | 2 | a0001c0004t0001g0302a0001c0004t0001g0303 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.111+3331A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429917 | ||||||
chr4:2429951
|
TC | T | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+3367delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429951 | |||||
chr4:2429995
|
G | A | 1 | a0001c0006t0002g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111+3409G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429995 | ||||||
chr4:2430062
|
A | G | 1 | a0002c0001t0001g0114 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+3476A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430062 | ||||||
chr4:2430062
|
ATAAACCA others(245): Show |
A | 1 | a0017c0019t0001g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.111+3495_111+3746d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430062 | |||||
chr4:2430081
|
G | C | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+3495G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430081 | ||||||
chr4:2430090
|
A | G | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+3504A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430090 | ||||||
chr4:2430108
|
A | G | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+3522A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430108 | ||||||
chr4:2430125
|
ATAAACCA others(182): Show |
A | 104 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(101): Show | 120 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.111+3602_111+3790d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430125 | |||||
chr4:2430152
|
C | T | 19 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(16): Show | 21 | HG01243.hp1 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.111+3566C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430152 | ||||||
chr4:2430153
|
GGACTGCG others(119): Show |
G | 8 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3602_111+3727d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430153 | |||||
chr4:2430188
|
A | G | 37 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(34): Show | 37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+3602A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430188 | ||||||
chr4:2430188
|
ATAAACCA others(119): Show |
A | 78 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(75): Show | 84 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.111+3684_111+3809d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430188 | |||||
chr4:2430188
|
ATAAACCA others(245): Show |
A | 17 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(14): Show | 20 | HG00544.hp2 HG02055.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.111+3684_111+3935d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430188 | |||||
chr4:2430207
|
CCGGACAG others(56): Show |
C | 1 | a0002c0001t0001g0135 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.111+3630_111+3692d others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430207 | |||||
chr4:2430216
|
GGACTGCG others(56): Show |
G | 3 | a0001c0003t0001g0021a0001c0003t0001g0127a0001c0006t0001g0128 | 4 | HG02615.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+3684_111+3746d others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430216 | |||||
chr4:2430240
|
T | C | 6 | a0001c0003t0001g0058a0001c0003t0001g0089a0001c0004t0001g0063others(3): Show | 6 | HG01261.hp1 HG02602.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+3654T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430240 | ||||||
chr4:2430243
|
CGCAATAC others(182): Show |
C | 26 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(23): Show | 27 | HG00735.hp2 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+3684_111+3872d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430243 | |||||
chr4:2430251
|
G | A | 7 | a0001c0002t0001g0062a0001c0003t0001g0016a0001c0003t0001g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3665G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430251 | ||||||
chr4:2430261
|
C | T | 33 | a0001c0002t0001g0134a0001c0002t0001g0142a0001c0002t0001g0143others(30): Show | 33 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.111+3675C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430261 | ||||||
chr4:2430270
|
G | C | 43 | a0001c0002t0001g0033a0001c0002t0001g0062a0001c0002t0001g0134others(40): Show | 44 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.111+3684G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430270 | ||||||
chr4:2430279
|
A | G | 7 | a0001c0002t0001g0062a0001c0003t0001g0016a0001c0003t0001g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3693A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430279 | ||||||
chr4:2430303
|
T | C | 6 | a0001c0002t0001g0062a0001c0003t0001g0016a0001c0003t0001g0126others(3): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+3717T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430303 | ||||||
chr4:2430314
|
G | A | 7 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(4): Show | 9 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+3728G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430314 | ||||||
chr4:2430333
|
C | G | 8 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3747C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430333 | ||||||
chr4:2430342
|
G | A | 8 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3756G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430342 | ||||||
chr4:2430342
|
G | GGACTGCG others(56): Show |
1 | a0001c0006t0002g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111+3809_111+3810i others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430342 | |||||
chr4:2430352
|
GAAATGCC others(120): Show |
G | 1 | a0001c0002t0001g0062 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.111+3769_111+3895d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430352 | |||||
chr4:2430366
|
T | C | 6 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(3): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3780T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430366 | ||||||
chr4:2430369
|
CGCAATAC others(56): Show |
C | 1 | a0001c0003t0001g0136 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.111+3846_111+3908d others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430369 | |||||
chr4:2430377
|
G | A | 254 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0033others(251): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.111+3791G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430377 | ||||||
chr4:2430396
|
C | G | 1 | a0016c0036t0002g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+3810C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430396 | ||||||
chr4:2430405
|
G | A | 1 | a0016c0036t0002g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+3819G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430405 | ||||||
chr4:2430429
|
T | C | 182 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0051others(179): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.111+3843T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430429 | ||||||
chr4:2430432
|
T | C | 226 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0033others(223): Show | 250 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.111+3846T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430432 | ||||||
chr4:2430440
|
G | A | 16 | a0001c0002t0001g0022a0001c0002t0001g0309a0001c0002t0001g0310others(13): Show | 17 | HG00609.hp1 HG00735.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.111+3854G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430440 | ||||||
chr4:2430450
|
C | G | 37 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(34): Show | 37 | HG00621.hp2 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+3864C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430450 | ||||||
chr4:2430461
|
G | A | 39 | a0001c0002t0001g0033a0001c0002t0001g0092a0001c0002t0001g0093others(36): Show | 39 | HG00621.hp2 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.111+3875G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430461 | ||||||
chr4:2430492
|
T | C | 19 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(16): Show | 22 | HG00544.hp2 HG00735.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.111+3906T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430492 | ||||||
chr4:2430503
|
G | A | 53 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(50): Show | 54 | HG00621.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.111+3917G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430503 | ||||||
chr4:2430576
|
T | C | 5 | a0001c0003t0001g0231a0001c0003t0001g0232a0002c0001t0001g0005others(2): Show | 7 | HG00544.hp2 HG02080.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+3990T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430576 | ||||||
chr4:2430594
|
A | G | 4 | a0001c0003t0001g0231a0001c0003t0001g0232a0002c0001t0001g0227others(1): Show | 4 | HG00544.hp2 HG02080.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+4008A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430594 | ||||||
chr4:2430642
|
A | C | 120 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0022others(117): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.111+4056A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430642 | ||||||
chr4:2430674
|
G | A | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+4088G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430674 | ||||||
chr4:2430697
|
C | T | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+4111C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430697 | ||||||
chr4:2430787
|
A | T | 1 | a0001c0002t0001g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111+4201A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430787 | ||||||
chr4:2430828
|
G | T | 282 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(279): Show | 310 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.111+4242G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430828 | ||||||
chr4:2430934
|
A | C | 1 | a0001c0006t0002g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111+4348A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430934 | ||||||
chr4:2431006
|
A | G | 1 | a0001c0004t0001g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.111+4420A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431006 | ||||||
chr4:2431055
|
G | C | 214 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0022others(211): Show | 241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.111+4469G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431055 | ||||||
chr4:2431091
|
G | A | 4 | a0002c0001t0001g0214a0002c0001t0001g0234a0002c0001t0001g0235others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+4505G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431091 | ||||||
chr4:2431134
|
C | T | 101 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(98): Show | 108 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.111+4548C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431134 | ||||||
chr4:2431296
|
G | C | 15 | a0001c0003t0001g0231a0001c0003t0001g0232a0002c0001t0001g0006others(12): Show | 17 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.111+4710G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431296 | ||||||
chr4:2431316
|
T | C | 270 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(267): Show | 298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.111+4730T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431316 | ||||||
chr4:2431331
|
G | T | 270 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(267): Show | 298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.111+4745G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431331 | ||||||
chr4:2431368
|
C | CA | 203 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0051others(200): Show | 229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.111+4794dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431368 | |||||
chr4:2431368
|
C | CAAAA | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+4791_111+4794d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431368 | |||||
chr4:2431472
|
A | C | 270 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(267): Show | 298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.111+4886A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431472 | ||||||
chr4:2431554
|
A | G | 113 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(110): Show | 133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.111+4968A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431554 | ||||||
chr4:2431574
|
A | T | 10 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(7): Show | 11 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+4988A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431574 | ||||||
chr4:2431676
|
C | G | 6 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(3): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+5090C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431676 | ||||||
chr4:2431699
|
A | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+5113A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431699 | ||||||
chr4:2431744
|
A | AT | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-5118dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431744 | |||||
chr4:2431744
|
AT | A | 163 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0033others(160): Show | 182 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.112-5118delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431744 | |||||
chr4:2431765
|
C | T | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.112-5109C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431765 | ||||||
chr4:2431790
|
C | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-5084C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431790 | ||||||
chr4:2431804
|
C | G | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.112-5070C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431804 | ||||||
chr4:2431821
|
A | G | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-5053A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431821 | ||||||
chr4:2431848
|
C | T | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.112-5026C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431848 | ||||||
chr4:2431970
|
G | A | 2 | a0001c0012t0001g0083a0001c0012t0001g0084 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.112-4904G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431970 | ||||||
chr4:2431973
|
C | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-4901C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431973 | ||||||
chr4:2432192
|
C | A | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-4682C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432192 | ||||||
chr4:2432368
|
G | A | 2 | a0002c0001t0001g0214a0002c0001t0001g0234 | 2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.112-4506G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432368 | ||||||
chr4:2432479
|
T | C | 1 | a0001c0002t0001g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.112-4395T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432479 | ||||||
chr4:2432585
|
C | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-4289C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432585 | ||||||
chr4:2432821
|
T | C | 270 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(267): Show | 298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.112-4053T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432821 | ||||||
chr4:2432981
|
CCCCCAGG | C | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-3881_112-3875d others(9): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2432981 | |||||
chr4:2433038
|
C | T | 4 | a0001c0003t0001g0218a0002c0001t0001g0002a0002c0001t0001g0017others(1): Show | 8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-3836C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433038 | ||||||
chr4:2433061
|
G | A | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.112-3813G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433061 | ||||||
chr4:2433062
|
G | A | 38 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(35): Show | 38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.112-3812G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433062 | ||||||
chr4:2433079
|
G | A | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-3795G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433079 | ||||||
chr4:2433118
|
CCTCA | C | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-3751_112-3748d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2433118 | |||||
chr4:2433176
|
G | C | 2 | a0001c0002t0001g0205a0001c0003t0001g0169 | 2 | HG01358.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.112-3698G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433176 | ||||||
chr4:2433309
|
G | A | 1 | a0001c0002t0001g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112-3565G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433309 | ||||||
chr4:2433351
|
C | T | 1 | a0001c0006t0002g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.112-3523C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433351 | ||||||
chr4:2433427
|
C | CG | 33 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0137others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.112-3438dupG | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2433427 | |||||
chr4:2433427
|
C | T | 2 | a0001c0002t0001g0056a0001c0002t0001g0062 | 2 | NA18986.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.112-3447C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433427 | ||||||
chr4:2433434
|
G | C | 11 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-3440G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433434 | ||||||
chr4:2433437
|
A | C | 1 | a0002c0005t0001g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.112-3437A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433437 | ||||||
chr4:2433628
|
C | T | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-3246C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433628 | ||||||
chr4:2433705
|
A | G | 2 | a0001c0002t0003g0306a0001c0002t0003g0312 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.112-3169A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433705 | ||||||
chr4:2433717
|
A | G | 1 | a0002c0001t0001g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.112-3157A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433717 | ||||||
chr4:2433803
|
T | G | 278 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0022others(275): Show | 305 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.112-3071T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433803 | ||||||
chr4:2433822
|
G | T | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.112-3052G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433822 | ||||||
chr4:2433875
|
G | A | 2 | a0001c0018t0001g0130a0001c0018t0001g0162 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.112-2999G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433875 | ||||||
chr4:2433889
|
G | A | 207 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0022others(204): Show | 232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.112-2985G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433889 | ||||||
chr4:2433904
|
T | C | 264 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(261): Show | 290 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.112-2970T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433904 | ||||||
chr4:2433942
|
G | A | 1 | a0001c0004t0001g0302 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.112-2932G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433942 | ||||||
chr4:2433951
|
G | A | 1 | a0001c0006t0002g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.112-2923G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433951 | ||||||
chr4:2434099
|
G | A | 1 | a0002c0005t0001g0244 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.112-2775G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434099 | ||||||
chr4:2434254
|
G | A | 37 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(34): Show | 37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.112-2620G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434254 | ||||||
chr4:2434315
|
C | A | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.112-2559C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434315 | ||||||
chr4:2434337
|
C | G | 14 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(11): Show | 15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-2537C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434337 | ||||||
chr4:2434443
|
G | A | 1 | a0002c0001t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.112-2431G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434443 | ||||||
chr4:2434530
|
G | A | 268 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0022others(265): Show | 295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.112-2344G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434530 | ||||||
chr4:2434644
|
G | A | 18 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(15): Show | 20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.112-2230G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434644 | ||||||
chr4:2434655
|
G | A | 1 | a0001c0003t0001g0126 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112-2219G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434655 | ||||||
chr4:2434715
|
G | A | 1 | a0001c0003t0005g0313 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.112-2159G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434715 | ||||||
chr4:2434726
|
T | C | 250 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0022others(247): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.112-2148T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434726 | ||||||
chr4:2435059
|
G | A | 2 | a0006c0028t0001g0170a0006c0029t0001g0171 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.112-1815G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435059 | ||||||
chr4:2435188
|
T | C | 14 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(11): Show | 15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-1686T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435188 | ||||||
chr4:2435261
|
C | T | 4 | a0001c0003t0001g0172a0001c0003t0001g0315a0006c0028t0001g0170others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-1613C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435261 | ||||||
chr4:2435298
|
G | GA | 25 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(22): Show | 28 | HG00735.hp1 HG01255.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.112-1559dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435298 | |||||
chr4:2435298
|
GA | G | 6 | a0001c0002t0001g0055a0001c0006t0002g0040a0002c0001t0001g0047others(3): Show | 6 | HG01256.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-1559delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435298 | |||||
chr4:2435299
|
A | G | 4 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-1575A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435299 | ||||||
chr4:2435470
|
A | G | 14 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(11): Show | 15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-1404A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435470 | ||||||
chr4:2435503
|
A | C | 2 | a0002c0001t0001g0272a0017c0019t0001g0230 | 2 | HG03492.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.112-1371A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435503 | ||||||
chr4:2435563
|
G | A | 195 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0051others(192): Show | 219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.112-1311G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435563 | ||||||
chr4:2435661
|
C | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-1213C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435661 | ||||||
chr4:2435725
|
G | T | 1 | a0001c0018t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-1149G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435725 | ||||||
chr4:2435807
|
C | CCAGCTAC others(20): Show |
1 | a0002c0005t0001g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.112-1043_112-1042i others(29): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435807 | |||||
chr4:2435807
|
CCAGCTAC others(21): Show |
C | 1 | a0002c0001t0001g0216 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.112-1013_112-986de others(29): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435807 | |||||
chr4:2435833
|
A | AAGCAGCT others(49): Show |
1 | a0002c0001t0001g0271 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.112-1014_112-1013i others(58): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435833 | |||||
chr4:2435833
|
A | AAGCAGCT others(77): Show |
37 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0289others(34): Show | 38 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.112-1014_112-1013i others(86): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435833 | |||||
chr4:2435833
|
A | AAGCAGCT others(105): Show |
3 | a0001c0003t0001g0010a0001c0003t0001g0054a0001c0003t0001g0081 | 3 | NA18964.hp1 NA18971.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.112-1014_112-1013i others(114): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435833 | |||||
chr4:2435861
|
A | AAGCAGCT others(161): Show |
7 | a0001c0002t0001g0022a0001c0002t0001g0309a0001c0002t0001g0310others(4): Show | 8 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-986_112-985ins others(168): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(273): Show |
3 | a0001c0002t0001g0049a0001c0002t0001g0314a0001c0021t0001g0308 | 3 | HG02451.hp1 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.112-986_112-985ins others(280): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(273): Show |
3 | a0001c0002t0001g0207a0001c0002t0001g0307a0001c0003t0005g0313 | 3 | HG01255.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.112-986_112-985ins others(280): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(49): Show |
47 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(44): Show | 48 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.112-986_112-985ins others(56): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(77): Show |
1 | a0001c0035t0001g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.112-986_112-985ins others(84): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(105): Show |
5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-986_112-985ins others(112): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(21): Show |
18 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(15): Show | 20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.112-901_112-874dup others(28): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(105): Show |
28 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0056others(25): Show | 30 | HG00099.hp1 HG00280.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-985_112-874dup others(112): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | AAGCAGCT others(161): Show |
4 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0006t0001g0012others(1): Show | 4 | HG01884.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(168): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | |||||
chr4:2435861
|
A | G | 109 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(106): Show | 128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.112-1013A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435861 | ||||||
chr4:2435883
|
G | GGTGGGGA others(77): Show |
1 | a0001c0003t0001g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.112-908_112-907ins others(84): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435883 | |||||
chr4:2435992
|
C | CGAGGTGG others(104): Show |
1 | a0001c0002t0001g0055 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.112-874_112-873ins others(111): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | |||||
chr4:2435992
|
C | CGAGGTGG others(161): Show |
9 | a0001c0002t0001g0096a0001c0002t0001g0100a0001c0003t0001g0058others(6): Show | 9 | HG01074.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(168): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | |||||
chr4:2435992
|
C | CGAGGTGG others(105): Show |
47 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0066others(44): Show | 48 | HG00408.hp1 HG00673.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(112): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | |||||
chr4:2435992
|
C | CGAGGTGG others(77): Show |
69 | a0001c0002t0001g0018a0001c0002t0001g0288a0001c0003t0001g0019others(66): Show | 81 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(84): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | |||||
chr4:2435992
|
C | CGAGGTGG others(179): Show |
4 | a0001c0003t0001g0231a0001c0003t0001g0232a0002c0001t0001g0227others(1): Show | 4 | HG00544.hp2 HG02080.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(186): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | |||||
chr4:2435992
|
C | CGAGGTGG others(49): Show |
1 | a0002c0001t0001g0270 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.112-874_112-873ins others(56): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | |||||
chr4:2435992
|
C | CGAGGTGG others(21): Show |
1 | a0002c0005t0001g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.112-874_112-873ins others(28): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | |||||
chr4:2435992
|
C | T | 141 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(138): Show | 146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.112-882C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435992 | ||||||
chr4:2436044
|
G | A | 1 | a0001c0004t0001g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112-830G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436044 | ||||||
chr4:2436080
|
TCA | T | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-793_112-792del others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436080 | ||||||
chr4:2436081
|
CA | C | 14 | a0001c0002t0001g0153a0001c0003t0001g0016a0001c0003t0001g0021others(11): Show | 16 | HG01516.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.112-779delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436081 | |||||
chr4:2436081
|
CAA | C | 99 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(96): Show | 106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.112-780_112-779del others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436081 | |||||
chr4:2436116
|
GAT | G | 51 | a0001c0002t0001g0004a0001c0002t0001g0033a0001c0002t0001g0134others(48): Show | 52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112-750_112-749del others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436116 | |||||
chr4:2436124
|
T | C | 1 | a0002c0005t0001g0102 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.112-750T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436124 | ||||||
chr4:2436165
|
T | G | 4 | a0002c0001t0001g0281a0002c0001t0001g0282a0002c0001t0001g0286others(1): Show | 4 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-709T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436165 | ||||||
chr4:2436251
|
G | A | 1 | a0002c0001t0001g0225 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.112-623G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436251 | ||||||
chr4:2436271
|
C | T | 1 | a0002c0001t0001g0241 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.112-603C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436271 | ||||||
chr4:2436299
|
G | A | 1 | a0002c0001t0001g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112-575G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436299 | ||||||
chr4:2436300
|
C | T | 1 | a0002c0001t0001g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112-574C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436300 | ||||||
chr4:2436634
|
ACTGCCTC others(5): Show |
A | 1 | a0001c0002t0001g0062 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.112-237_112-226del others(12): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436634 | |||||
chr4:2436639
|
CTCA | C | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.112-229_112-227del others(3): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436639 | |||||
chr4:2436650
|
C | T | 1 | a0002c0001t0001g0061 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112-224C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436650 | ||||||
chr4:2436765
|
T | C | 284 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(281): Show | 312 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.112-109T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436765 | ||||||
chr4:2436856
|
C | T | 1 | a0001c0002t0001g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112-18C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436856 | ||||||
chr4:2436861
|
G | C | 1 | a0003c0010t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.112-13G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436861 | ||||||
chr4:2437202
|
T | C | 195 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0022others(192): Show | 217 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.256+184T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437202 | ||||||
chr4:2437550
|
G | A | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.257-520G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437550 | ||||||
chr4:2437607
|
C | T | 2 | a0001c0018t0001g0130a0001c0018t0001g0162 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.257-463C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437607 | ||||||
chr4:2437672
|
C | T | 1 | a0001c0025t0001g0269 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.257-398C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437672 | ||||||
chr4:2437696
|
C | T | 1 | a0001c0003t0005g0313 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.257-374C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437696 | ||||||
chr4:2437943
|
A | G | 283 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(280): Show | 311 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.257-127A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437943 | ||||||
chr4:2437974
|
G | A | 37 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(34): Show | 37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.257-96G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437974 | ||||||
chr4:2437999
|
G | A | 1 | a0001c0035t0001g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.257-71G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437999 | ||||||
chr4:2438011
|
G | A | 125 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(122): Show | 145 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.257-59G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2438011 | ||||||
chr4:2438018
|
G | C | 18 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(15): Show | 20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.257-52G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2438018 | ||||||
chr4:2438029
|
C | CT | 156 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(153): Show | 175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.257-41_257-40insT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2438029 | ||||||
chr4:2438173
|
C | A | 125 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0049others(122): Show | 144 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.351+9C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438173 | ||||||
chr4:2438205
|
G | A | 94 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(91): Show | 100 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.351+41G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438205 | ||||||
chr4:2438226
|
C | T | 6 | a0001c0002t0001g0049a0001c0002t0001g0207a0001c0002t0001g0307others(3): Show | 6 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+62C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438226 | ||||||
chr4:2438238
|
G | C | 107 | a0001c0002t0001g0018a0001c0002t0001g0287a0001c0002t0001g0288others(104): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.351+74G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438238 | ||||||
chr4:2438294
|
A | G | 160 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0134others(157): Show | 180 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.351+130A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438294 | ||||||
chr4:2438315
|
G | T | 35 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(32): Show | 35 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.351+151G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438315 | ||||||
chr4:2438324
|
G | A | 31 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(28): Show | 31 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.351+160G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438324 | ||||||
chr4:2438344
|
A | G | 18 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(15): Show | 19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+180A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438344 | ||||||
chr4:2438348
|
T | C | 125 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0049others(122): Show | 144 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.351+184T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438348 | ||||||
chr4:2438363
|
T | C | 18 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(15): Show | 19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+199T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438363 | ||||||
chr4:2438364
|
A | G | 18 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(15): Show | 20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.351+200A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438364 | ||||||
chr4:2438408
|
G | A | 6 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(3): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+244G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438408 | ||||||
chr4:2438408
|
G | C | 103 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0051others(100): Show | 110 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.351+244G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438408 | ||||||
chr4:2438420
|
A | G | 18 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(15): Show | 19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+256A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438420 | ||||||
chr4:2438424
|
G | A | 18 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(15): Show | 19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+260G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438424 | ||||||
chr4:2438508
|
C | T | 1 | a0001c0002t0001g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+344C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438508 | ||||||
chr4:2438533
|
G | A | 162 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(159): Show | 181 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.351+369G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438533 | ||||||
chr4:2438542
|
G | A | 89 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0053others(86): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.351+378G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438542 | ||||||
chr4:2438553
|
C | T | 2 | a0002c0005t0002g0036a0002c0005t0002g0037 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.351+389C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438553 | ||||||
chr4:2438797
|
C | A | 51 | a0001c0002t0001g0033a0001c0002t0001g0134a0001c0002t0001g0137others(48): Show | 53 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.351+633C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438797 | ||||||
chr4:2438806
|
C | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(10): Show | 14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.351+642C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438806 | ||||||
chr4:2438897
|
A | C | 108 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0051others(105): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.351+733A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438897 | ||||||
chr4:2438902
|
G | A | 18 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(15): Show | 20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.351+738G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438902 | ||||||
chr4:2438943
|
T | G | 1 | a0002c0001t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.351+779T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438943 | ||||||
chr4:2438986
|
C | T | 12 | a0001c0003t0002g0039a0001c0004t0002g0043a0001c0004t0002g0044others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+822C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438986 | ||||||
chr4:2439010
|
C | T | 6 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(3): Show | 7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+846C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439010 | ||||||
chr4:2439011
|
G | A | 5 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+847G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439011 | ||||||
chr4:2439091
|
T | C | 163 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0033others(160): Show | 182 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.351+927T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439091 | ||||||
chr4:2439194
|
A | G | 4 | a0001c0002t0001g0033a0001c0002t0001g0137a0001c0003t0001g0136others(1): Show | 4 | HG00609.hp1 HG00621.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1030A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439194 | ||||||
chr4:2439255
|
G | A | 1 | a0001c0004t0001g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.351+1091G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439255 | ||||||
chr4:2439591
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.351+1427G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439591 | ||||||
chr4:2439596
|
C | T | 12 | a0001c0002t0001g0022a0001c0002t0001g0049a0001c0002t0001g0207others(9): Show | 13 | HG01255.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.351+1432C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439596 | ||||||
chr4:2439771
|
C | A | 1 | a0001c0002t0001g0062 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.351+1607C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439771 | ||||||
chr4:2439773
|
A | C | 1 | a0001c0002t0001g0062 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.351+1609A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439773 | ||||||
chr4:2439847
|
AT | A | 12 | a0001c0002t0001g0094a0001c0002t0001g0205a0001c0002t0001g0219others(9): Show | 12 | HG01074.hp2 HG02083.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+1697delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2439847 | |||||
chr4:2439867
|
G | A | 14 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(11): Show | 15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+1703G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439867 | ||||||
chr4:2439889
|
G | T | 122 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(119): Show | 131 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.351+1725G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439889 | ||||||
chr4:2439893
|
G | A | 2 | a0001c0002t0001g0004a0001c0003t0001g0004 | 3 | HG02258.hp1 HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.351+1729G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439893 | ||||||
chr4:2439912
|
C | T | 7 | a0001c0002t0001g0022a0001c0002t0001g0309a0001c0002t0001g0310others(4): Show | 8 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+1748C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439912 | ||||||
chr4:2439975
|
C | T | 1 | a0001c0003t0001g0132 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.351+1811C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439975 | ||||||
chr4:2439998
|
A | G | 14 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(11): Show | 15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+1834A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439998 | ||||||
chr4:2440062
|
G | A | 1 | a0005c0009t0001g0159 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.351+1898G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440062 | ||||||
chr4:2440134
|
G | A | 2 | a0001c0002t0001g0176a0001c0002t0001g0177 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.351+1970G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440134 | ||||||
chr4:2440149
|
C | CT | 8 | a0001c0003t0001g0132a0001c0003t0001g0141a0002c0001t0001g0233others(5): Show | 8 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2000dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(4): Show |
2 | a0001c0002t0001g0049a0001c0002t0003g0306 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.351+1990_351+2000d others(13): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(5): Show |
9 | a0001c0002t0001g0022a0001c0002t0001g0207a0001c0002t0001g0307others(6): Show | 10 | HG02486.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+1989_351+2000d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(6): Show |
6 | a0001c0003t0001g0023a0001c0003t0001g0024a0001c0003t0001g0025others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1988_351+2000d others(15): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(7): Show |
7 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0006t0002g0034others(4): Show | 7 | HG01109.hp2 HG01891.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+1987_351+2000d others(16): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(8): Show |
10 | a0001c0002t0001g0066a0001c0004t0001g0178a0001c0004t0002g0043others(7): Show | 10 | HG00673.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+1986_351+2000d others(17): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(9): Show |
64 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0055others(61): Show | 70 | HG00280.hp1 HG00408.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.351+2000_351+2001i others(18): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(10): Show |
27 | a0001c0002t0001g0011a0001c0002t0001g0079a0001c0002t0001g0100others(24): Show | 29 | HG00099.hp1 HG00735.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.351+2000_351+2001i others(19): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(11): Show |
2 | a0001c0004t0001g0086a0001c0012t0001g0084 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.351+2000_351+2001i others(20): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440149
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0001g0062 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.351+2000_351+2001i others(21): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | |||||
chr4:2440177
|
C | T | 1 | a0002c0001t0001g0235 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+2013C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440177 | ||||||
chr4:2440178
|
G | A | 123 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(120): Show | 132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.351+2014G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440178 | ||||||
chr4:2440208
|
A | G | 123 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(120): Show | 132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.351+2044A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440208 | ||||||
chr4:2440239
|
C | T | 2 | a0001c0002t0001g0066a0001c0002t0001g0111 | 2 | HG00673.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.351+2075C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440239 | ||||||
chr4:2440247
|
C | T | 121 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(118): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.351+2083C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440247 | ||||||
chr4:2440290
|
G | A | 4 | a0001c0003t0001g0218a0002c0001t0001g0002a0002c0001t0001g0017others(1): Show | 8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+2126G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440290 | ||||||
chr4:2440307
|
C | T | 1 | a0001c0004t0001g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.351+2143C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440307 | ||||||
chr4:2440336
|
C | T | 124 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(121): Show | 133 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.351+2172C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440336 | ||||||
chr4:2440438
|
G | A | 6 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0028others(3): Show | 7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2274G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440438 | ||||||
chr4:2440565
|
G | C | 123 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(120): Show | 132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.351+2401G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440565 | ||||||
chr4:2440627
|
C | T | 1 | a0002c0001t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.351+2463C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440627 | ||||||
chr4:2441011
|
T | C | 3 | a0001c0003t0002g0039a0001c0006t0002g0040a0001c0006t0002g0042 | 3 | HG02257.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.352-2119T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441011 | ||||||
chr4:2441196
|
C | T | 3 | a0001c0003t0001g0016a0001c0003t0001g0126a0001c0003t0001g0129 | 4 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-1934C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441196 | ||||||
chr4:2441243
|
C | T | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.352-1887C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441243 | ||||||
chr4:2441273
|
T | C | 2 | a0001c0018t0001g0130a0001c0018t0001g0162 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.352-1857T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441273 | ||||||
chr4:2441330
|
G | A | 1 | a0001c0003t0001g0231 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.352-1800G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441330 | ||||||
chr4:2441359
|
C | T | 2 | a0001c0018t0001g0130a0001c0018t0001g0162 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.352-1771C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441359 | ||||||
chr4:2441372
|
C | CA | 147 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0033others(144): Show | 168 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.352-1739dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2441372 | |||||
chr4:2441372
|
CA | C | 104 | a0001c0002t0001g0011a0001c0002t0001g0022a0001c0002t0001g0049others(101): Show | 111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.352-1739delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2441372 | |||||
chr4:2441477
|
C | G | 12 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(9): Show | 13 | HG02135.hp1 HG02155.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.352-1653C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441477 | ||||||
chr4:2441478
|
C | G | 4 | a0001c0003t0001g0218a0002c0001t0001g0002a0002c0001t0001g0017others(1): Show | 8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1652C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441478 | ||||||
chr4:2441520
|
G | A | 1 | a0001c0004t0001g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-1610G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441520 | ||||||
chr4:2441558
|
C | T | 2 | a0001c0003t0002g0039a0001c0006t0002g0040 | 2 | HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.352-1572C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441558 | ||||||
chr4:2441644
|
C | T | 6 | a0001c0003t0002g0039a0001c0006t0002g0034a0001c0006t0002g0040others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.352-1486C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441644 | ||||||
chr4:2441862
|
C | T | 1 | a0001c0003t0001g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.352-1268C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441862 | ||||||
chr4:2441894
|
G | T | 1 | a0002c0001t0001g0299 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.352-1236G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441894 | ||||||
chr4:2441916
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.352-1214G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441916 | ||||||
chr4:2442002
|
G | T | 1 | a0001c0003t0001g0074 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.352-1128G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442002 | ||||||
chr4:2442374
|
G | A | 1 | a0001c0034t0001g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.352-756G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442374 | ||||||
chr4:2442425
|
G | A | 1 | a0003c0007t0001g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.352-705G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442425 | ||||||
chr4:2442453
|
A | T | 1 | a0001c0006t0002g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.352-677A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442453 | ||||||
chr4:2442459
|
G | A | 2 | a0002c0001t0001g0251a0002c0001t0001g0304 | 2 | NA18944.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.352-671G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442459 | ||||||
chr4:2442467
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.352-663G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442467 | ||||||
chr4:2442639
|
G | A | 1 | a0008c0011t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.352-491G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442639 | ||||||
chr4:2442670
|
G | T | 1 | a0013c0020t0001g0073 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.352-460G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442670 | ||||||
chr4:2442682
|
G | A | 2 | a0001c0003t0001g0028a0001c0003t0001g0174 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.352-448G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442682 | ||||||
chr4:2442861
|
TGGCCTTG others(161): Show |
T | 2 | a0001c0004t0001g0302a0001c0004t0001g0303 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.352-231_352-64del | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442861 | |||||
chr4:2442881
|
TCACTGGG others(59): Show |
T | 220 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(217): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.352-138_352-73delT others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442881 | |||||
chr4:2442881
|
TCACTGGG others(125): Show |
T | 8 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-204_352-73del | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442881 | |||||
chr4:2442908
|
G | A | 2 | a0001c0004t0001g0067a0001c0004t0001g0212 | 2 | HG01106.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.352-222G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442908 | ||||||
chr4:2442917
|
TCACTGGG others(23): Show |
T | 2 | a0001c0004t0001g0178a0001c0035t0001g0030 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.352-204_352-175del others(30): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442917 | |||||
chr4:2442922
|
GGGGTGCT others(58): Show |
G | 17 | a0001c0004t0001g0041a0001c0004t0001g0063a0001c0004t0001g0067others(14): Show | 17 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.352-204_352-140del others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442922 | |||||
chr4:2442934
|
G | T | 1 | a0001c0002t0001g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.352-196G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442934 | ||||||
chr4:2442947
|
C | CCACTGGG others(334): Show |
1 | a0002c0001t0001g0088 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.352-66_352-65insTG others(339): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442947 | |||||
chr4:2442954
|
G | A | 1 | a0001c0015t0001g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.352-176G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442954 | ||||||
chr4:2442962
|
G | A | 1 | a0001c0006t0002g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.352-168G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442962 | ||||||
chr4:2442983
|
TCACTGGG others(23): Show |
T | 1 | a0001c0006t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-138_352-109del others(30): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442983 | |||||
chr4:2443007
|
G | GGGCAGGG others(176): Show |
1 | a0001c0003t0001g0026 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.352-121_352-120ins others(183): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2443007 | |||||
chr4:2443013
|
C | CT | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.352-117_352-116ins others(1): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2443013 | ||||||
chr4:2443018
|
G | GGGGGTGC others(64): Show |
2 | a0001c0003t0001g0025a0001c0003t0001g0027 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.352-64_352-63insGC others(69): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2443018 | |||||
chr4:2443259
|
G | A | 1 | a0001c0004t0001g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.464+17G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443259 | ||||||
chr4:2443291
|
A | G | 7 | a0002c0001t0001g0239a0002c0001t0001g0264a0002c0005t0001g0226others(4): Show | 7 | HG00438.hp1 HG00597.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.464+49A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443291 | ||||||
chr4:2443308
|
G | A | 1 | a0001c0003t0001g0293 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464+66G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443308 | ||||||
chr4:2443440
|
A | C | 127 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(124): Show | 136 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.464+198A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443440 | ||||||
chr4:2443505
|
C | T | 67 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(64): Show | 74 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.464+263C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443505 | ||||||
chr4:2443555
|
G | A | 1 | a0002c0031t0001g0294 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.464+313G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443555 | ||||||
chr4:2443661
|
G | A | 16 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0002g0043others(13): Show | 17 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.464+419G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443661 | ||||||
chr4:2443676
|
G | A | 3 | a0001c0003t0001g0016a0001c0003t0001g0126a0001c0003t0001g0129 | 4 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+434G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443676 | ||||||
chr4:2443848
|
A | G | 23 | a0001c0003t0001g0028a0001c0003t0001g0174a0001c0004t0001g0041others(20): Show | 23 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.464+606A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443848 | ||||||
chr4:2443902
|
G | A | 2 | a0001c0012t0001g0083a0001c0012t0001g0084 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.464+660G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443902 | ||||||
chr4:2444180
|
C | A | 2 | a0006c0028t0001g0170a0006c0029t0001g0171 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464+938C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444180 | ||||||
chr4:2444385
|
A | G | 1 | a0001c0015t0001g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.465-746A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444385 | ||||||
chr4:2444388
|
G | C | 3 | a0001c0003t0001g0016a0001c0003t0001g0126a0001c0003t0001g0129 | 4 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.465-743G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444388 | ||||||
chr4:2444403
|
C | T | 3 | a0001c0002t0001g0100a0001c0004t0001g0206a0001c0015t0001g0285 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.465-728C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444403 | ||||||
chr4:2444413
|
A | G | 3 | a0001c0002t0001g0100a0001c0004t0001g0206a0001c0015t0001g0285 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.465-718A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444413 | ||||||
chr4:2444447
|
C | T | 3 | a0002c0001t0001g0107a0002c0001t0001g0112a0002c0001t0001g0122 | 3 | NA18950.hp1 NA18986.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.465-684C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444447 | ||||||
chr4:2444498
|
C | G | 1 | a0001c0004t0001g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.465-633C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444498 | ||||||
chr4:2444805
|
G | A | 225 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(222): Show | 244 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.465-326G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444805 | ||||||
chr4:2444833
|
C | T | 226 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(223): Show | 245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.465-298C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444833 | ||||||
chr4:2444895
|
C | T | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.465-236C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444895 | ||||||
chr4:2444917
|
G | A | 226 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(223): Show | 245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.465-214G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444917 | ||||||
chr4:2444986
|
G | A | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.465-145G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444986 | ||||||
chr4:2444993
|
G | C | 94 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(91): Show | 103 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.465-138G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444993 | ||||||
chr4:2444998
|
C | G | 48 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0049others(45): Show | 49 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.465-133C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444998 | ||||||
chr4:2445092
|
G | A | 1 | a0001c0003t0001g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.465-39G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2445092 | ||||||
chr4:2445554
|
T | A | 2 | a0001c0003t0001g0087a0001c0003t0001g0119 | 2 | NA18961.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.642+246T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445554 | ||||||
chr4:2445626
|
C | T | 1 | a0001c0003t0001g0315 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.642+318C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445626 | ||||||
chr4:2445627
|
G | A | 1 | a0001c0021t0001g0308 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.642+319G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445627 | ||||||
chr4:2445676
|
A | G | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+368A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445676 | ||||||
chr4:2445875
|
G | A | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+567G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445875 | ||||||
chr4:2445960
|
A | G | 12 | a0001c0002t0001g0018a0001c0002t0001g0176a0001c0002t0001g0177others(9): Show | 13 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.642+652A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445960 | ||||||
chr4:2445980
|
A | C | 1 | a0016c0036t0002g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.642+672A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445980 | ||||||
chr4:2446001
|
C | T | 1 | a0014c0022t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.642+693C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446001 | ||||||
chr4:2446050
|
G | A | 2 | a0001c0003t0001g0028a0001c0003t0001g0174 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.642+742G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446050 | ||||||
chr4:2446249
|
C | G | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+941C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446249 | ||||||
chr4:2446249
|
C | T | 26 | a0001c0002t0001g0100a0001c0003t0001g0028a0001c0003t0001g0174others(23): Show | 26 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.642+941C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446249 | ||||||
chr4:2446285
|
CCTGCCTA others(4): Show |
C | 3 | a0001c0004t0001g0086a0001c0004t0001g0305a0001c0004t0001g0311 | 3 | HG02647.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.642+987_642+997del others(11): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446285 | |||||
chr4:2446368
|
G | GTTA | 8 | a0001c0003t0001g0081a0001c0003t0001g0108a0001c0004t0002g0043others(5): Show | 8 | HG02683.hp2 HG02698.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+1099_642+1101d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
G | GTTATTA | 8 | a0001c0002t0001g0055a0001c0002t0001g0057a0001c0002t0001g0076others(5): Show | 8 | HG02257.hp2 NA18948.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+1096_642+1101d others(8): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
G | GTTATTAT others(2): Show |
8 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(5): Show | 10 | HG02135.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+1093_642+1101d others(11): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
GTTA | G | 22 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0220others(19): Show | 24 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+1099_642+1101d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
GTTATTA | G | 4 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030others(1): Show | 4 | HG01109.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+1096_642+1101d others(8): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
GTTATTAT others(5): Show |
G | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+1090_642+1101d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
GTTATTAT others(8): Show |
G | 7 | a0001c0003t0001g0172a0001c0003t0001g0315a0001c0004t0001g0178others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+1087_642+1101d others(17): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
GTTATTAT others(11): Show |
G | 218 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(215): Show | 237 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.642+1084_642+1101d others(20): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446368
|
GTTATTAT others(17): Show |
G | 5 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027others(2): Show | 5 | HG01192.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1078_642+1101d others(26): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | |||||
chr4:2446371
|
A | G | 1 | a0001c0003t0001g0231 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.642+1063A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446371 | ||||||
chr4:2446374
|
A | G | 2 | a0001c0003t0001g0120a0001c0003t0001g0121 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.642+1066A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446374 | ||||||
chr4:2446420
|
T | A | 5 | a0002c0001t0001g0223a0002c0001t0001g0252a0002c0001t0001g0270others(2): Show | 5 | NA18944.hp2 NA18952.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1112T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446420 | ||||||
chr4:2446424
|
G | A | 7 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(4): Show | 9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.642+1116G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446424 | ||||||
chr4:2446449
|
G | A | 1 | a0001c0035t0001g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.642+1141G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446449 | ||||||
chr4:2446517
|
C | T | 1 | a0006c0028t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.642+1209C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446517 | ||||||
chr4:2446518
|
G | A | 1 | a0002c0001t0001g0228 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.642+1210G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446518 | ||||||
chr4:2446593
|
A | T | 1 | a0002c0001t0001g0270 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.642+1285A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446593 | ||||||
chr4:2446662
|
T | A | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+1354T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446662 | ||||||
chr4:2446726
|
A | G | 1 | a0001c0002t0001g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.642+1418A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446726 | ||||||
chr4:2446808
|
G | C | 1 | a0001c0003t0001g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.642+1500G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446808 | ||||||
chr4:2446812
|
G | GATGA | 7 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(4): Show | 9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.642+1508_642+1511d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446812 | |||||
chr4:2446816
|
A | AATGG | 103 | a0001c0003t0001g0019a0001c0003t0001g0087a0001c0003t0001g0104others(100): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.642+1528_642+1531d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446816 | |||||
chr4:2446836
|
G | C | 1 | a0005c0009t0001g0156 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.642+1528G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446836 | ||||||
chr4:2446931
|
G | T | 1 | a0001c0002t0001g0118 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.642+1623G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446931 | ||||||
chr4:2447095
|
GATGGATG others(19): Show |
G | 1 | a0009c0038t0001g0292 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.642+1802_642+1827d others(28): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447095 | |||||
chr4:2447105
|
T | C | 3 | a0001c0002t0001g0051a0001c0002t0001g0145a0001c0002t0001g0146 | 3 | NA18946.hp1 NA18992.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.642+1797T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447105 | ||||||
chr4:2447145
|
G | T | 1 | a0001c0002t0001g0289 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.642+1837G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447145 | ||||||
chr4:2447146
|
A | G | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+1838A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447146 | ||||||
chr4:2447195
|
T | A | 23 | a0001c0003t0001g0028a0001c0003t0001g0174a0001c0004t0001g0041others(20): Show | 23 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.642+1887T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447195 | ||||||
chr4:2447215
|
T | C | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+1907T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447215 | ||||||
chr4:2447224
|
GCATGGAA others(53): Show |
G | 1 | a0001c0006t0002g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.642+1933_642+1992d others(62): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447224 | |||||
chr4:2447258
|
C | CTGGA | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+1971_642+1974d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447258 | |||||
chr4:2447279
|
T | C | 5 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030others(2): Show | 5 | HG01243.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1971T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447279 | ||||||
chr4:2447442
|
T | C | 1 | a0001c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.642+2134T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447442 | ||||||
chr4:2447474
|
G | T | 99 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(96): Show | 108 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.642+2166G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447474 | ||||||
chr4:2447503
|
G | A | 3 | a0001c0004t0001g0086a0001c0004t0001g0305a0001c0004t0001g0311 | 3 | HG02647.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.643-2167G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447503 | ||||||
chr4:2447614
|
T | C | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.643-2056T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447614 | ||||||
chr4:2447645
|
G | GTGGA | 4 | a0001c0006t0001g0012a0001c0006t0001g0098a0001c0006t0001g0099others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-2004_643-2001d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447645 | |||||
chr4:2447645
|
GTGGATGG others(5): Show |
G | 1 | a0003c0007t0001g0052 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.643-2012_643-2001d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447645 | |||||
chr4:2447809
|
AATGG | A | 96 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(93): Show | 105 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.643-1852_643-1849d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447809 | |||||
chr4:2447818
|
A | G | 141 | a0001c0002t0001g0100a0001c0003t0001g0016a0001c0003t0001g0019others(138): Show | 158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.643-1852A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447818 | ||||||
chr4:2447834
|
A | G | 2 | a0001c0003t0001g0028a0001c0003t0001g0174 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.643-1836A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447834 | ||||||
chr4:2447913
|
GTGAA | G | 26 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0010others(23): Show | 31 | HG01074.hp1 HG01074.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.643-1750_643-1747d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447913 | |||||
chr4:2447916
|
AATGAATG others(21): Show |
A | 3 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030 | 3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.643-1750_643-1723d others(30): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447916 | |||||
chr4:2447917
|
ATGAATGG others(5): Show |
A | 65 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(62): Show | 69 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.643-1750_643-1739d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447917 | |||||
chr4:2447929
|
G | GTGGA | 10 | a0001c0002t0001g0095a0001c0003t0001g0028a0001c0003t0001g0174others(7): Show | 10 | HG01891.hp1 HG02015.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-1693_643-1690d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | |||||
chr4:2447929
|
GTGGA | G | 159 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(156): Show | 178 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.643-1693_643-1690d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | |||||
chr4:2447929
|
GTGGATGG others(1): Show |
G | 30 | a0001c0002t0001g0100a0001c0002t0001g0208a0001c0002t0001g0210others(27): Show | 30 | HG00099.hp2 HG00597.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.643-1697_643-1690d others(10): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | |||||
chr4:2447929
|
GTGGATGG others(5): Show |
G | 9 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(6): Show | 11 | HG00609.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-1701_643-1690d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | |||||
chr4:2447929
|
GTGGATGG others(9): Show |
G | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.643-1705_643-1690d others(18): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | |||||
chr4:2447937
|
A | G | 66 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(63): Show | 70 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.643-1733A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447937 | ||||||
chr4:2447953
|
A | G | 3 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030 | 3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.643-1717A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447953 | ||||||
chr4:2448004
|
G | A | 7 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(4): Show | 9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.643-1666G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448004 | ||||||
chr4:2448020
|
A | AATGGATG others(1): Show |
87 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(84): Show | 96 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.643-1634_643-1627d others(10): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2448020 | |||||
chr4:2448020
|
A | AATGGATG others(5): Show |
10 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-1638_643-1627d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2448020 | |||||
chr4:2448077
|
A | T | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.643-1593A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448077 | ||||||
chr4:2448184
|
C | A | 4 | a0001c0006t0001g0012a0001c0006t0001g0098a0001c0006t0001g0099others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1486C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448184 | ||||||
chr4:2448255
|
C | T | 1 | a0001c0024t0001g0185 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.643-1415C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448255 | ||||||
chr4:2448332
|
A | G | 1 | a0001c0003t0002g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.643-1338A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448332 | ||||||
chr4:2448403
|
G | A | 2 | a0001c0006t0001g0029a0001c0006t0001g0031 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.643-1267G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448403 | ||||||
chr4:2448614
|
G | A | 1 | a0001c0003t0001g0191 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.643-1056G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448614 | ||||||
chr4:2448710
|
T | C | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.643-960T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448710 | ||||||
chr4:2448746
|
G | A | 6 | a0005c0009t0001g0156a0005c0009t0001g0158a0005c0009t0001g0159others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-924G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448746 | ||||||
chr4:2448755
|
C | CG | 5 | a0001c0003t0001g0139a0001c0003t0001g0155a0002c0001t0001g0225others(2): Show | 5 | HG00735.hp1 HG02135.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-911dupG | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2448755 | |||||
chr4:2448957
|
T | C | 1 | a0002c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-713T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448957 | ||||||
chr4:2449165
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.643-505G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449165 | ||||||
chr4:2449207
|
G | C | 1 | a0002c0001t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.643-463G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449207 | ||||||
chr4:2449307
|
C | T | 1 | a0001c0003t0001g0184 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.643-363C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449307 | ||||||
chr4:2449308
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.643-362G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449308 | ||||||
chr4:2449884
|
G | A | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.724-50G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 7/15 | chr4 | 2449884 | ||||||
chr4:2449911
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.724-23G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 7/15 | chr4 | 2449911 | ||||||
chr4:2450085
|
C | T | 1 | a0001c0003t0001g0131 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.795+80C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450085 | ||||||
chr4:2450196
|
G | A | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.795+191G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450196 | ||||||
chr4:2450222
|
A | G | 227 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(224): Show | 246 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.795+217A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450222 | ||||||
chr4:2450360
|
C | T | 84 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(81): Show | 86 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.795+355C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450360 | ||||||
chr4:2450474
|
G | A | 1 | a0001c0018t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.795+469G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450474 | ||||||
chr4:2450489
|
G | A | 1 | a0001c0003t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.796-458G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450489 | ||||||
chr4:2450601
|
G | A | 14 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0002g0043others(11): Show | 15 | HG01109.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.796-346G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450601 | ||||||
chr4:2450870
|
G | A | 2 | a0002c0001t0001g0106a0002c0001t0001g0253 | 2 | HG02155.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.796-77G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450870 | ||||||
chr4:2451064
|
AC | A | 82 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(79): Show | 84 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.867+50delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 2451064 | |||||
chr4:2451086
|
C | T | 1 | a0001c0004t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.867+68C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/15 | chr4 | 2451086 | ||||||
chr4:2451206
|
T | C | 227 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(224): Show | 246 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.868-58T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/15 | chr4 | 2451206 | ||||||
chr4:2451452
|
G | A | 1 | a0017c0019t0001g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.956+100G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451452 | ||||||
chr4:2451497
|
G | A | 19 | a0001c0004t0001g0041a0001c0004t0001g0063a0001c0004t0001g0067others(16): Show | 19 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.956+145G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451497 | ||||||
chr4:2451519
|
T | A | 1 | a0002c0001t0001g0088 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.956+167T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451519 | ||||||
chr4:2451548
|
G | A | 217 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(214): Show | 236 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.956+196G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451548 | ||||||
chr4:2451630
|
C | G | 223 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(220): Show | 242 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.956+278C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451630 | ||||||
chr4:2451698
|
T | C | 226 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(223): Show | 245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.956+346T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451698 | ||||||
chr4:2451724
|
C | T | 7 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.956+372C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451724 | ||||||
chr4:2451733
|
AGGCTGTG others(3): Show |
A | 223 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0033others(220): Show | 242 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.956+384_956+393del others(10): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr4 | 2451733 | |||||
chr4:2451744
|
G | A | 1 | a0001c0003t0001g0014 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.956+392G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451744 | ||||||
chr4:2451869
|
T | C | 1 | a0001c0003t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.957-273T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451869 | ||||||
chr4:2451949
|
C | T | 46 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0049others(43): Show | 47 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.957-193C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451949 | ||||||
chr4:2451989
|
C | T | 4 | a0002c0001t0001g0223a0002c0001t0001g0270a0002c0001t0001g0296others(1): Show | 4 | NA18944.hp2 NA18977.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-153C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451989 | ||||||
chr4:2452056
|
A | G | 5 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(2): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.957-86A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2452056 | ||||||
chr4:2452362
|
G | C | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+16G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452362 | ||||||
chr4:2452408
|
G | A | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+62G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452408 | ||||||
chr4:2452456
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1161+110G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452456 | ||||||
chr4:2452468
|
G | A | 1 | a0001c0002t0001g0182 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1161+122G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452468 | ||||||
chr4:2452605
|
C | T | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+259C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452605 | ||||||
chr4:2452682
|
C | T | 5 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(2): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+336C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452682 | ||||||
chr4:2452687
|
A | C | 1 | a0002c0001t0001g0241 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1161+341A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452687 | ||||||
chr4:2452693
|
T | G | 2 | a0001c0003t0001g0060a0001c0003t0001g0101 | 2 | NA18947.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1161+347T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452693 | ||||||
chr4:2452893
|
T | A | 1 | a0001c0003t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1161+547T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452893 | ||||||
chr4:2452920
|
G | A | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1161+574G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452920 | ||||||
chr4:2452924
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1161+578A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452924 | ||||||
chr4:2452979
|
C | T | 107 | a0001c0002t0001g0033a0001c0003t0001g0019a0001c0003t0001g0087others(104): Show | 122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1161+633C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452979 | ||||||
chr4:2452988
|
G | T | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1161+642G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452988 | ||||||
chr4:2453007
|
G | A | 1 | a0001c0006t0002g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1161+661G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453007 | ||||||
chr4:2453038
|
G | A | 5 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(2): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+692G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453038 | ||||||
chr4:2453050
|
G | A | 1 | a0016c0036t0002g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1161+704G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453050 | ||||||
chr4:2453347
|
G | C | 1 | a0011c0037t0001g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1161+1001G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453347 | ||||||
chr4:2453353
|
C | T | 91 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(88): Show | 100 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1161+1007C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453353 | ||||||
chr4:2453391
|
G | C | 91 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(88): Show | 100 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1161+1045G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453391 | ||||||
chr4:2453456
|
G | A | 2 | a0002c0001t0001g0237a0002c0001t0001g0242 | 2 | HG02056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1161+1110G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453456 | ||||||
chr4:2453636
|
A | G | 25 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0003t0001g0028others(22): Show | 25 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1161+1290A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453636 | ||||||
chr4:2453664
|
T | TTC | 320 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(317): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1161+1319_1161+132 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453664 | |||||
chr4:2453741
|
C | CT | 25 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0100others(22): Show | 25 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1161+1410dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453741 | |||||
chr4:2453741
|
CT | C | 20 | a0001c0002t0001g0004a0001c0002t0001g0145a0001c0002t0001g0298others(17): Show | 21 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1161+1410delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453741 | |||||
chr4:2453741
|
CTT | C | 85 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(82): Show | 93 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1161+1409_1161+141 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453741 | |||||
chr4:2453816
|
AT | A | 97 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(94): Show | 108 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1161+1485delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453816 | |||||
chr4:2453880
|
C | T | 3 | a0002c0001t0001g0222a0002c0001t0001g0246a0002c0001t0001g0255 | 3 | HG00642.hp2 HG00735.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1161+1534C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453880 | ||||||
chr4:2453903
|
TC | T | 3 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030 | 3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1161+1560delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453903 | |||||
chr4:2453915
|
G | A | 1 | a0002c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1161+1569G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453915 | ||||||
chr4:2453935
|
T | G | 91 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(88): Show | 100 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1161+1589T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453935 | ||||||
chr4:2454087
|
C | T | 1 | a0001c0003t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1161+1741C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454087 | ||||||
chr4:2454237
|
G | A | 1 | a0001c0006t0001g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1161+1891G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454237 | ||||||
chr4:2454335
|
CTG | C | 3 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030 | 3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1161+1993_1161+199 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454335 | |||||
chr4:2454528
|
GA | G | 73 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(70): Show | 81 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1161+2184delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454528 | |||||
chr4:2454531
|
C | T | 73 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(70): Show | 81 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1161+2185C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454531 | ||||||
chr4:2454581
|
C | T | 1 | a0002c0001t0001g0246 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1161+2235C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454581 | ||||||
chr4:2454581
|
CT | C | 109 | a0001c0002t0001g0056a0001c0002t0001g0219a0001c0003t0001g0019others(106): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1161+2247delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454581 | |||||
chr4:2454582
|
T | C | 1 | a0002c0001t0001g0246 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1161+2236T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454582 | ||||||
chr4:2454593
|
T | G | 20 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0004t0001g0041others(17): Show | 20 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1161+2247T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454593 | ||||||
chr4:2454593
|
T | TG | 6 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030others(3): Show | 6 | HG01074.hp1 HG01243.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+2248dupG | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454593 | |||||
chr4:2454594
|
G | T | 28 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0150others(25): Show | 28 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1161+2248G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454594 | ||||||
chr4:2454594
|
GT | G | 21 | a0001c0002t0001g0004a0001c0002t0001g0100a0001c0003t0001g0004others(18): Show | 22 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1161+2263delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454594 | |||||
chr4:2454595
|
T | C | 7 | a0001c0002t0001g0150a0001c0002t0001g0151a0001c0002t0001g0152others(4): Show | 7 | HG01358.hp2 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+2249T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454595 | ||||||
chr4:2454595
|
T | G | 70 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(67): Show | 78 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1161+2249T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454595 | ||||||
chr4:2454596
|
T | G | 17 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0002g0043others(14): Show | 18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1161+2250T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454596 | ||||||
chr4:2454701
|
A | G | 1 | a0001c0004t0001g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1161+2355A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454701 | ||||||
chr4:2454845
|
C | G | 10 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0006t0001g0029others(7): Show | 11 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1161+2499C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454845 | ||||||
chr4:2455075
|
T | G | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1161+2729T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455075 | ||||||
chr4:2455081
|
G | A | 1 | a0001c0003t0001g0133 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1161+2735G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455081 | ||||||
chr4:2455184
|
G | A | 2 | a0001c0006t0001g0167a0001c0006t0001g0168 | 2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1161+2838G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455184 | ||||||
chr4:2455228
|
A | C | 1 | a0003c0010t0001g0080 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1161+2882A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455228 | ||||||
chr4:2455262
|
T | G | 1 | a0001c0003t0001g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1161+2916T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455262 | ||||||
chr4:2455410
|
C | T | 2 | a0001c0003t0001g0087a0001c0003t0001g0119 | 2 | NA18961.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1161+3064C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455410 | ||||||
chr4:2455510
|
TA | T | 95 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(92): Show | 104 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1161+3171delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2455510 | |||||
chr4:2455795
|
T | A | 2 | a0001c0006t0001g0029a0001c0006t0001g0031 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1162-2928T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455795 | ||||||
chr4:2455964
|
G | C | 19 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0001g0178others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-2759G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455964 | ||||||
chr4:2456223
|
C | T | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1162-2500C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456223 | ||||||
chr4:2456351
|
A | G | 96 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(93): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1162-2372A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456351 | ||||||
chr4:2456372
|
G | GA | 96 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(93): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1162-2348dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456372 | |||||
chr4:2456408
|
G | A | 1 | a0001c0003t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1162-2315G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456408 | ||||||
chr4:2456508
|
G | A | 1 | a0001c0004t0001g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1162-2215G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456508 | ||||||
chr4:2456607
|
C | T | 5 | a0001c0018t0001g0130a0001c0018t0001g0162a0001c0035t0001g0030others(2): Show | 5 | HG01243.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-2116C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456607 | ||||||
chr4:2456666
|
T | G | 1 | a0002c0005t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1162-2057T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456666 | ||||||
chr4:2456763
|
C | T | 2 | a0001c0012t0001g0083a0001c0012t0001g0084 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1162-1960C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456763 | ||||||
chr4:2456808
|
C | T | 1 | a0001c0003t0001g0184 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1162-1915C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456808 | ||||||
chr4:2456810
|
C | T | 2 | a0002c0001t0001g0211a0002c0001t0001g0299 | 2 | NA18961.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1162-1913C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456810 | ||||||
chr4:2456813
|
C | T | 74 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(71): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1162-1910C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456813 | ||||||
chr4:2456846
|
C | T | 2 | a0001c0002t0001g0004a0001c0003t0001g0004 | 3 | HG02258.hp1 HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1162-1877C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456846 | ||||||
chr4:2456878
|
G | A | 320 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0018others(317): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1162-1845G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456878 | ||||||
chr4:2456923
|
A | T | 19 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0001g0178others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1800A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456923 | ||||||
chr4:2456950
|
C | CT | 64 | a0001c0002t0001g0011a0001c0002t0001g0055a0001c0002t0001g0057others(61): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1162-1753dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456950 | |||||
chr4:2456950
|
CT | C | 147 | a0001c0002t0001g0004a0001c0002t0001g0093a0001c0002t0001g0100others(144): Show | 162 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1162-1753delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456950 | |||||
chr4:2456950
|
CTT | C | 9 | a0001c0002t0001g0092a0002c0001t0001g0007a0002c0001t0001g0107others(6): Show | 10 | HG00609.hp2 HG01975.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1162-1754_1162-175 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456950 | |||||
chr4:2456957
|
T | C | 1 | a0001c0006t0001g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-1766T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456957 | ||||||
chr4:2457001
|
G | A | 19 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0001g0178others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1722G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457001 | ||||||
chr4:2457141
|
G | A | 1 | a0003c0007t0001g0297 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1162-1582G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457141 | ||||||
chr4:2457206
|
G | A | 1 | a0002c0001t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1162-1517G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457206 | ||||||
chr4:2457395
|
G | A | 19 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0001g0178others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1328G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457395 | ||||||
chr4:2457423
|
A | G | 96 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(93): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1162-1300A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457423 | ||||||
chr4:2457426
|
G | A | 19 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0004t0001g0178others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1297G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457426 | ||||||
chr4:2457473
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0004t0001g0188 | 3 | HG03491.hp2 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1162-1250C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457473 | ||||||
chr4:2457635
|
G | T | 1 | a0002c0001t0001g0228 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1162-1088G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457635 | ||||||
chr4:2457654
|
AC | A | 5 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(2): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162-1068delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457654 | ||||||
chr4:2457708
|
T | C | 74 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(71): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1162-1015T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457708 | ||||||
chr4:2457731
|
C | G | 22 | a0001c0002t0001g0004a0001c0003t0001g0004a0001c0003t0001g0025others(19): Show | 23 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1162-992C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457731 | ||||||
chr4:2457768
|
C | T | 5 | a0001c0002t0001g0100a0001c0004t0001g0206a0001c0012t0001g0083others(2): Show | 5 | HG02145.hp2 HG02647.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-955C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457768 | ||||||
chr4:2457781
|
C | T | 1 | a0002c0001t0001g0239 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1162-942C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457781 | ||||||
chr4:2457782
|
G | A | 2 | a0001c0012t0001g0083a0001c0012t0001g0084 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1162-941G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457782 | ||||||
chr4:2457839
|
G | T | 1 | a0001c0002t0001g0195 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1162-884G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457839 | ||||||
chr4:2457875
|
G | A | 9 | a0001c0003t0001g0016a0001c0003t0001g0021a0001c0003t0001g0126others(6): Show | 11 | HG01884.hp1 HG01975.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162-848G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457875 | ||||||
chr4:2458017
|
C | A | 4 | a0001c0006t0001g0012a0001c0006t0001g0098a0001c0006t0001g0099others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-706C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458017 | ||||||
chr4:2458083
|
C | G | 2 | a0001c0012t0001g0083a0001c0012t0001g0084 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1162-640C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458083 | ||||||
chr4:2458127
|
G | A | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1162-596G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458127 | ||||||
chr4:2458171
|
T | C | 48 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0049others(45): Show | 49 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1162-552T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458171 | ||||||
chr4:2458200
|
G | T | 1 | a0001c0002t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1162-523G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458200 | ||||||
chr4:2458295
|
T | A | 1 | a0001c0015t0001g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1162-428T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458295 | ||||||
chr4:2458316
|
A | G | 1 | a0001c0006t0001g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-407A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458316 | ||||||
chr4:2458450
|
A | G | 3 | a0001c0002t0001g0100a0001c0004t0001g0206a0001c0015t0001g0285 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1162-273A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458450 | ||||||
chr4:2458464
|
T | C | 23 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0003t0001g0028others(20): Show | 23 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1162-259T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458464 | ||||||
chr4:2458475
|
A | G | 1 | a0002c0001t0001g0279 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1162-248A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458475 | ||||||
chr4:2458542
|
C | T | 2 | a0001c0002t0001g0137a0001c0004t0001g0178 | 2 | HG00621.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1162-181C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458542 | ||||||
chr4:2458565
|
C | T | 66 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(63): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1162-158C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458565 | ||||||
chr4:2458574
|
T | C | 77 | a0001c0002t0001g0011a0001c0002t0001g0053a0001c0002t0001g0055others(74): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1162-149T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458574 | ||||||
chr4:2458636
|
C | A | 1 | a0001c0003t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1162-87C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458636 | ||||||
chr4:2458913
|
G | A | 1 | a0001c0002t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1303+49G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2458913 | ||||||
chr4:2459037
|
G | T | 1 | a0001c0003t0001g0315 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1304-70G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2459037 | ||||||
chr4:2459076
|
A | G | 219 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0053others(216): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1304-31A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2459076 | ||||||
chr4:2459098
|
G | A | 1 | a0001c0015t0001g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1304-9G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2459098 | ||||||
chr4:2459408
|
A | C | 2 | a0001c0003t0001g0097a0001c0004t0001g0086 | 2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1455+150A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459408 | ||||||
chr4:2459417
|
G | A | 1 | a0002c0005t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1455+159G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459417 | ||||||
chr4:2459452
|
C | T | 1 | a0001c0004t0001g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1455+194C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459452 | ||||||
chr4:2459482
|
A | C | 3 | a0001c0003t0001g0126a0001c0012t0001g0083a0001c0012t0001g0084 | 3 | HG02055.hp2 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1455+224A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459482 | ||||||
chr4:2459614
|
A | G | 2 | a0001c0003t0001g0072a0013c0020t0001g0073 | 2 | NA18946.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1455+356A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459614 | ||||||
chr4:2459664
|
T | A | 5 | a0001c0003t0001g0021a0001c0003t0001g0028a0001c0003t0001g0174others(2): Show | 6 | HG02723.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456-373T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459664 | ||||||
chr4:2459759
|
A | G | 304 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0022others(301): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1456-278A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459759 | ||||||
chr4:2459780
|
G | A | 1 | a0001c0003t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1456-257G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459780 | ||||||
chr4:2460268
|
C | A | 5 | a0001c0003t0001g0026a0001c0004t0001g0189a0001c0004t0001g0204others(2): Show | 5 | HG00639.hp1 HG02004.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661+26C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460268 | ||||||
chr4:2460422
|
A | G | 1 | a0001c0032t0001g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1661+180A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460422 | ||||||
chr4:2460522
|
C | T | 2 | a0001c0035t0001g0030a0016c0036t0002g0035 | 2 | HG01109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1661+280C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460522 | ||||||
chr4:2460899
|
C | T | 1 | a0002c0001t0001g0144 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1661+657C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460899 | ||||||
chr4:2460900
|
G | A | 1 | a0001c0003t0001g0133 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1661+658G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460900 | ||||||
chr4:2460921
|
C | G | 1 | a0001c0006t0001g0165 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1661+679C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460921 | ||||||
chr4:2460973
|
G | A | 5 | a0001c0002t0001g0199a0001c0002t0001g0205a0003c0010t0001g0080others(2): Show | 5 | HG02055.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1661+731G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460973 | ||||||
chr4:2461054
|
G | A | 9 | a0001c0002t0001g0022a0001c0002t0001g0142a0001c0002t0001g0287others(6): Show | 10 | HG01891.hp2 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1661+812G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461054 | ||||||
chr4:2461137
|
C | T | 2 | a0001c0003t0001g0028a0001c0003t0001g0174 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1661+895C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461137 | ||||||
chr4:2461233
|
G | A | 8 | a0001c0003t0001g0026a0001c0004t0001g0189a0001c0004t0001g0204others(5): Show | 8 | HG00639.hp1 HG02004.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1661+991G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461233 | ||||||
chr4:2461337
|
G | A | 267 | a0001c0002t0001g0004a0001c0002t0001g0022a0001c0002t0001g0033others(264): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1661+1095G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461337 | ||||||
chr4:2461361
|
G | A | 1 | a0001c0006t0001g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1662-1082G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461361 | ||||||
chr4:2461526
|
A | G | 4 | a0005c0009t0001g0156a0005c0009t0001g0158a0005c0009t0001g0159others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662-917A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461526 | ||||||
chr4:2461594
|
A | T | 15 | a0001c0003t0001g0028a0001c0003t0001g0174a0001c0004t0001g0086others(12): Show | 15 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1662-849A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461594 | ||||||
chr4:2461909
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1662-534G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461909 | ||||||
chr4:2461942
|
G | A | 12 | a0001c0003t0001g0028a0001c0003t0001g0174a0001c0004t0001g0086others(9): Show | 12 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1662-501G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461942 | ||||||
chr4:2461978
|
T | TA | 22 | a0001c0003t0001g0026a0001c0003t0001g0028a0001c0003t0001g0174others(19): Show | 22 | HG00639.hp1 HG01243.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.1662-458dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 2461978 | |||||
chr4:2461982
|
A | C | 5 | a0001c0003t0001g0058a0001c0003t0001g0089a0001c0003t0001g0097others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662-461A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461982 | ||||||
chr4:2462088
|
T | A | 1 | a0001c0024t0001g0185 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1662-355T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462088 | ||||||
chr4:2462117
|
A | G | 1 | a0001c0003t0001g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1662-326A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462117 | ||||||
chr4:2462248
|
T | C | 2 | a0002c0001t0001g0085a0002c0001t0001g0265 | 2 | HG02083.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1662-195T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462248 | ||||||
chr4:2462295
|
G | A | 3 | a0001c0004t0002g0043a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662-148G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462295 | ||||||
chr4:2462368
|
G | A | 2 | a0001c0003t0001g0028a0001c0003t0001g0174 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1662-75G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462368 | ||||||
chr4:2462657
|
T | A | 8 | a0003c0007t0001g0065a0003c0007t0001g0071a0003c0007t0001g0250others(5): Show | 8 | HG02698.hp1 HG02738.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1824+52T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462657 | ||||||
chr4:2462673
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1824+68G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462673 | ||||||
chr4:2462689
|
C | A | 1 | a0001c0002t0001g0154 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1824+84C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462689 | ||||||
chr4:2462689
|
C | G | 2 | a0001c0002t0001g0288a0001c0002t0001g0289 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1824+84C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462689 | ||||||
chr4:2462718
|
G | T | 1 | a0001c0003t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1825-92G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462718 |