geneid | 115548 |
---|---|
ensemblid | ENSG00000157107.14 |
hgncid | 25180 |
symbol | FCHO2 |
name | FCH and mu domain containing endocytic adaptor 2 |
refseq_nuc | NM_138782.3 |
refseq_prot | NP_620137.2 |
ensembl_nuc | ENST00000430046.7 |
ensembl_prot | ENSP00000393776.2 |
mane_status | MANE Select |
chr | chr5 |
start | 72956041 |
end | 73090522 |
strand | + |
ver | v1.2 |
region | chr5:72956041-73090522 |
region5000 | chr5:72951041-73095522 |
regionname0 | FCHO2_chr5_72956041_73090522 |
regionname5000 | FCHO2_chr5_72951041_73095522 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 810 | 211 | 42 | 39 | 101 | 5 | 22 | 73 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0002 | 0/0 | 810 | 71 | 24 | 9 | 30 | 1 | 7 | 20 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0003 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0004 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0005 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0006 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2433 | 115 | 15 | 25 | 57 | 2 | 15 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0002 | 0/0 | 2433 | 71 | 24 | 9 | 30 | 1 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0003 | 0/0 | 2433 | 51 | 25 | 10 | 7 | 2 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0004 | 0/1 | 2433 | 38 | 2 | 3 | 31 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0005 | 0/0 | 2433 | 5 | 0 | 0 | 5 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0006 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0007 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0008 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0009 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0010 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
c0011 | 0/0 | 2433 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2489 | 107 | 14 | 22 | 54 | 2 | 15 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0002 | 1/0 | 2489 | 72 | 24 | 9 | 30 | 1 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0003 | 0/0 | 2489 | 47 | 9 | 3 | 35 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0004 | 0/0 | 2489 | 27 | 1 | 9 | 7 | 2 | 8 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0005 | 0/0 | 2489 | 9 | 9 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0006 | 0/0 | 2489 | 4 | 4 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0007 | 0/0 | 2489 | 4 | 1 | 3 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0008 | 0/0 | 2489 | 3 | 3 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0009 | 0/1 | 2489 | 2 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0010 | 0/0 | 2489 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0011 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0012 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0013 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0014 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0015 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0016 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0017 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0018 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
t0019 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2433 | 115 | 15 | 25 | 57 | 2 | 15 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003 | 0/0 | 2433 | 51 | 25 | 10 | 7 | 2 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0004 | 0/1 | 2433 | 38 | 2 | 3 | 31 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0005 | 0/0 | 2433 | 5 | 0 | 0 | 5 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0009 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0010 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0002c0002 | 0/0 | 2433 | 71 | 24 | 9 | 30 | 1 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0003c0006 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0004c0008 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0005c0011 | 0/0 | 2433 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0006c0007 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4921 | 106 | 14 | 21 | 54 | 2 | 15 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0001t0002 | 1/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0001t0007 | 0/0 | 4921 | 4 | 1 | 3 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0001t0013 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0001t0015 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0001t0018 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0001t0019 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0003 | 0/0 | 4921 | 6 | 6 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0004 | 0/0 | 4921 | 26 | 1 | 9 | 7 | 2 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0005 | 0/0 | 4921 | 8 | 8 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0006 | 0/0 | 4921 | 4 | 4 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0008 | 0/0 | 4921 | 3 | 3 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0010 | 0/0 | 4921 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0011 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0003t0016 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0004t0003 | 0/0 | 4921 | 34 | 2 | 3 | 29 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0004t0009 | 0/1 | 4921 | 2 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0004t0012 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0004t0014 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0005t0003 | 0/0 | 4921 | 4 | 0 | 0 | 4 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0005t0017 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0009t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0001c0010t0003 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0002c0002t0002 | 0/0 | 4921 | 71 | 24 | 9 | 30 | 1 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0003c0006t0005 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0004c0008t0003 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0005c0011t0004 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
a0006c0007t0003 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | copy fasta | chr5 | 72951041 | 73095522 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0002g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0015g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0018g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0001t0019g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0003t0016g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0009g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0009g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0012g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0004t0014g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0005t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0005t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0005t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0005t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0005t0017g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0009t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0001c0010t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0003c0006t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0004c0008t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0005c0011t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
a0006c0007t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0004 | g0086 | EUR | GBR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | GBR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00423 | hp1 | a0001 | c0003 | t0004 | g0095 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00438 | hp2 | a0001 | c0003 | t0004 | g0096 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00558 | hp2 | a0001 | c0004 | t0003 | g0266 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00609 | hp1 | a0001 | c0004 | t0003 | g0264 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00609 | hp2 | a0001 | c0003 | t0004 | g0081 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00621 | hp2 | a0001 | c0004 | t0003 | g0239 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00735 | hp1 | a0001 | c0004 | t0003 | g0243 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01069 | hp2 | a0001 | c0003 | t0004 | g0073 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01071 | hp1 | a0001 | c0003 | t0004 | g0072 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01081 | hp1 | a0001 | c0004 | t0003 | g0246 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0231 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01099 | hp2 | a0001 | c0003 | t0004 | g0089 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01106 | hp2 | a0001 | c0003 | t0016 | g0097 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01168 | hp1 | a0001 | c0003 | t0004 | g0085 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01168 | hp2 | a0001 | c0009 | t0001 | g0127 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01169 | hp2 | a0001 | c0003 | t0004 | g0084 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01192 | hp1 | a0001 | c0001 | t0015 | g0167 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01192 | hp2 | a0001 | c0003 | t0004 | g0071 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01255 | hp2 | a0001 | c0003 | t0004 | g0076 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01261 | hp2 | a0001 | c0003 | t0004 | g0094 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01496 | hp2 | a0001 | c0001 | t0007 | g0228 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01934 | hp1 | a0001 | c0001 | t0007 | g0230 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01934 | hp2 | a0001 | c0004 | t0003 | g0267 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02027 | hp2 | a0001 | c0004 | t0003 | g0272 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02056 | hp1 | a0001 | c0004 | t0012 | g0265 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02071 | hp1 | a0001 | c0004 | t0003 | g0274 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02074 | hp1 | a0001 | c0003 | t0004 | g0082 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02074 | hp2 | a0001 | c0004 | t0003 | g0275 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02080 | hp1 | a0001 | c0004 | t0003 | g0270 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0061 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02145 | hp2 | a0001 | c0003 | t0003 | g0281 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | CDX | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02257 | hp1 | a0001 | c0003 | t0008 | g0110 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02280 | hp1 | a0001 | c0004 | t0003 | g0245 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02280 | hp2 | a0001 | c0003 | t0011 | g0232 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02451 | hp1 | a0001 | c0003 | t0005 | g0002 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02451 | hp2 | a0001 | c0003 | t0005 | g0106 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02523 | hp1 | a0001 | c0004 | t0003 | g0238 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02572 | hp1 | a0001 | c0003 | t0006 | g0103 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02602 | hp2 | a0001 | c0003 | t0004 | g0075 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02615 | hp1 | a0001 | c0003 | t0010 | g0010 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02615 | hp2 | a0001 | c0003 | t0004 | g0093 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02622 | hp1 | a0001 | c0003 | t0005 | g0234 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02630 | hp1 | a0001 | c0003 | t0005 | g0235 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02630 | hp2 | a0001 | c0003 | t0010 | g0009 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02723 | hp1 | a0003 | c0006 | t0005 | g0003 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02809 | hp2 | a0004 | c0008 | t0003 | g0280 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02818 | hp1 | a0001 | c0003 | t0006 | g0102 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02965 | hp2 | a0001 | c0003 | t0003 | g0100 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03017 | hp2 | a0005 | c0011 | t0004 | g0090 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03041 | hp2 | a0001 | c0003 | t0006 | g0101 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03098 | hp2 | a0001 | c0003 | t0005 | g0108 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0279 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03139 | hp2 | a0001 | c0003 | t0008 | g0112 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0277 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03486 | hp2 | a0001 | c0003 | t0005 | g0109 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03491 | hp1 | a0001 | c0003 | t0004 | g0087 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03516 | hp1 | a0001 | c0003 | t0008 | g0111 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03654 | hp2 | a0001 | c0003 | t0004 | g0091 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03710 | hp2 | a0001 | c0003 | t0004 | g0074 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0022 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04115 | hp2 | a0001 | c0003 | t0004 | g0088 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0039 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0092 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG04228 | hp2 | a0001 | c0003 | t0004 | g0080 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18747 | hp1 | a0001 | c0004 | t0003 | g0276 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18906 | hp1 | a0001 | c0003 | t0003 | g0099 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18939 | hp1 | a0001 | c0005 | t0003 | g0248 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18940 | hp2 | a0001 | c0004 | t0003 | g0255 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18941 | hp2 | a0001 | c0004 | t0003 | g0247 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18942 | hp2 | a0001 | c0004 | t0003 | g0256 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18945 | hp2 | a0001 | c0004 | t0003 | g0271 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18946 | hp1 | a0001 | c0004 | t0003 | g0261 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18951 | hp2 | a0001 | c0004 | t0014 | g0236 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18954 | hp2 | a0006 | c0007 | t0003 | g0268 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18960 | hp2 | a0001 | c0004 | t0003 | g0273 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18965 | hp2 | a0001 | c0004 | t0003 | g0249 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18966 | hp2 | a0001 | c0005 | t0003 | g0258 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18971 | hp1 | a0001 | c0005 | t0017 | g0253 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18982 | hp2 | a0001 | c0004 | t0003 | g0284 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18984 | hp1 | a0001 | c0003 | t0004 | g0079 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18984 | hp2 | a0001 | c0004 | t0003 | g0250 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18989 | hp2 | a0001 | c0010 | t0003 | g0251 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18992 | hp2 | a0001 | c0004 | t0003 | g0263 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18998 | hp1 | a0001 | c0005 | t0003 | g0254 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA18999 | hp2 | a0001 | c0005 | t0003 | g0257 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19001 | hp2 | a0001 | c0004 | t0003 | g0242 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19004 | hp2 | a0001 | c0004 | t0003 | g0240 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19005 | hp1 | a0001 | c0004 | t0003 | g0260 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19010 | hp1 | a0001 | c0004 | t0003 | g0244 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19030 | hp1 | a0001 | c0003 | t0006 | g0104 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0070 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19054 | hp2 | a0001 | c0004 | t0003 | g0262 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19060 | hp1 | a0001 | c0004 | t0003 | g0269 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19062 | hp1 | a0001 | c0004 | t0003 | g0285 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19064 | hp2 | a0001 | c0001 | t0019 | g0158 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19068 | hp1 | a0001 | c0001 | t0018 | g0226 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19068 | hp2 | a0001 | c0004 | t0003 | g0237 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19082 | hp1 | a0001 | c0004 | t0003 | g0241 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19082 | hp2 | a0001 | c0001 | t0013 | g0193 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19084 | hp1 | a0001 | c0003 | t0004 | g0083 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19090 | hp2 | a0001 | c0003 | t0004 | g0078 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA19091 | hp2 | a0001 | c0004 | t0003 | g0259 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20129 | hp1 | a0001 | c0003 | t0005 | g0105 | AFR | ASW | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20752 | hp2 | a0001 | c0004 | t0009 | g0282 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20805 | hp1 | a0001 | c0003 | t0004 | g0077 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | GIH | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | GIH | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01123 | hp1 | a0001 | c0003 | t0004 | g0098 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02109 | hp1 | a0001 | c0003 | t0005 | g0107 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0065 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | USA | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0229 | AFR | USA | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA21309 | hp1 | a0001 | c0004 | t0003 | g0252 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
NA21309 | hp2 | a0001 | c0003 | t0003 | g0278 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0009 | g0283 | REF | REF | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0023 | REF | REF | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72990838
|
G | A | 1 | a0006 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.469G>A | p.Gly157Arg | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/26 | 525/4921 | 469/2433 | 157/810 | chr5 | 72990838 | ||
chr5:73017229
|
A | G | 1 | a0005 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.717A>G | p.Ile239Met | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/26 | 773/4921 | 717/2433 | 239/810 | chr5 | 73017229 | ||
chr5:73017239
|
G | A | 1 | a0004 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.727G>A | p.Ala243Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/26 | 783/4921 | 727/2433 | 243/810 | chr5 | 73017239 | ||
chr5:73052445
|
A | G | 1 | a0002 | 71 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(68): Show |
missense_variant | MODERATE | c.1111A>G | p.Met371Val | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/26 | 1167/4921 | 1111/2433 | 371/810 | chr5 | 73052445 | ||
chr5:73081754
|
A | AACAATTG others(36): Show |
1 | a0001 | 1 | NA19082.hp2 | frameshift_variant | HIGH | c.1981-27_1996dupCAA others(40): Show |
p.Ile666fs | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/26 | 2053/4921 | 1997/2433 | 666/810 | INFO_REALIGN_3_PRIME | chr5 | 73081754 | |
chr5:73087637
|
A | G | 1 | a0003 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.2294A>G | p.Lys765Arg | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 25/26 | 2350/4921 | 2294/2433 | 765/810 | chr5 | 73087637 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72990586
|
G | A | 1 | a0003c0006 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.309G>A | p.Lys103Lys | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 4/26 | 365/4921 | 309/2433 | 103/810 | chr5 | 72990586 | ||
chr5:73051396
|
A | G | 8 | a0001c0003a0001c0004a0001c0005others(5): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
synonymous_variant | LOW | c.987A>G | p.Thr329Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/26 | 1043/4921 | 987/2433 | 329/810 | chr5 | 73051396 | ||
chr5:73056078
|
A | G | 4 | a0001c0004a0001c0005a0001c0010others(1): Show | 45 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
synonymous_variant | LOW | c.1224A>G | p.Thr408Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/26 | 1280/4921 | 1224/2433 | 408/810 | chr5 | 73056078 | ||
chr5:73058502
|
T | C | 2 | a0001c0005a0001c0010 | 6 | NA18939.hp1 NA18966.hp2 NA18971.hp1 others(3): Show |
synonymous_variant | LOW | c.1323T>C | p.Ser441Ser | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/26 | 1379/4921 | 1323/2433 | 441/810 | chr5 | 73058502 | ||
chr5:73081875
|
A | G | 1 | a0001c0010 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.2073A>G | p.Lys691Lys | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/26 | 2129/4921 | 2073/2433 | 691/810 | chr5 | 73081875 | ||
chr5:73087644
|
G | A | 1 | a0001c0009 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.2301G>A | p.Thr767Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 25/26 | 2357/4921 | 2301/2433 | 767/810 | chr5 | 73087644 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:73088233
|
C | G | 1 | a0001c0001t0019 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 143 | chr5 | 73088233 | |||||
chr5:73088427
|
C | T | 1 | a0001c0001t0018 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 337 | chr5 | 73088427 | |||||
chr5:73088428
|
A | G | 1 | a0001c0005t0017 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 338 | chr5 | 73088428 | |||||
chr5:73088435
|
C | T | 1 | a0001c0001t0007 | 4 | HG01081.hp2 HG01496.hp2 HG01934.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*345C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 345 | chr5 | 73088435 | |||||
chr5:73088441
|
C | T | 1 | a0001c0003t0008 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 351 | chr5 | 73088441 | |||||
chr5:73088496
|
A | G | 1 | a0001c0003t0010 | 2 | HG02615.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*406A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 406 | chr5 | 73088496 | |||||
chr5:73088496
|
A | T | 1 | a0001c0003t0006 | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*406A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 406 | chr5 | 73088496 | |||||
chr5:73088868
|
A | G | 1 | a0001c0003t0016 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 778 | chr5 | 73088868 | |||||
chr5:73089026
|
C | T | 4 | a0001c0001t0015a0001c0003t0004a0001c0003t0016others(1): Show | 29 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*936C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 936 | chr5 | 73089026 | |||||
chr5:73089176
|
A | G | 1 | a0001c0004t0014 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1086 | chr5 | 73089176 | |||||
chr5:73089231
|
A | G | 7 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(4): Show | 115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1141A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1141 | chr5 | 73089231 | |||||
chr5:73089317
|
T | C | 4 | a0001c0001t0015a0001c0003t0004a0001c0003t0016others(1): Show | 29 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1227T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1227 | chr5 | 73089317 | |||||
chr5:73089402
|
T | C | 1 | a0001c0003t0011 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1312T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1312 | chr5 | 73089402 | |||||
chr5:73089626
|
A | T | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1536 | chr5 | 73089626 | |||||
chr5:73089877
|
A | G | 1 | a0001c0003t0011 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1787 | chr5 | 73089877 | |||||
chr5:73090068
|
C | T | 1 | a0001c0004t0009 | 2 | NA20752.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1978C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1978 | chr5 | 73090068 | |||||
chr5:73090086
|
A | G | 1 | a0001c0004t0012 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1996 | chr5 | 73090086 | |||||
chr5:73090087
|
A | G | 20 | a0001c0001t0015a0001c0003t0003a0001c0003t0004others(17): Show | 100 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1997A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1997 | chr5 | 73090087 | |||||
chr5:73090124
|
A | T | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2034A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2034 | chr5 | 73090124 | |||||
chr5:73090226
|
T | A | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2136T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2136 | chr5 | 73090226 | |||||
chr5:73090231
|
A | T | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2141A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2141 | chr5 | 73090231 | |||||
chr5:73090232
|
T | C | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2142T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2142 | chr5 | 73090232 | |||||
chr5:73090312
|
A | G | 11 | a0001c0003t0003a0001c0003t0008a0001c0004t0003others(8): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2222A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2222 | chr5 | 73090312 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72956206
|
C | T | 2 | a0001c0004t0003g0284a0001c0004t0003g0285 | 2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.33+77C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956206 | ||||||
chr5:72956207
|
G | GGGC | 50 | a0001c0003t0003g0277a0001c0003t0003g0278a0001c0003t0003g0279others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.33+91_33+93dupGGC | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72956207 | |||||
chr5:72956294
|
C | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.33+165C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956294 | ||||||
chr5:72956480
|
C | T | 1 | a0002c0002t0002g0233 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.33+351C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956480 | ||||||
chr5:72956536
|
C | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.33+407C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956536 | ||||||
chr5:72956648
|
A | G | 118 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(115): Show | 118 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.33+519A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956648 | ||||||
chr5:72956787
|
C | T | 4 | a0001c0001t0001g0116a0002c0002t0002g0113a0002c0002t0002g0114others(1): Show | 4 | HG01928.hp2 HG02300.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+658C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956787 | ||||||
chr5:72956888
|
C | A | 1 | a0001c0004t0014g0236 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.33+759C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956888 | ||||||
chr5:72956896
|
G | GT | 12 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.33+778dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72956896 | |||||
chr5:72957232
|
A | AT | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.33+1106dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72957232 | |||||
chr5:72957236
|
C | T | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.33+1107C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957236 | ||||||
chr5:72957237
|
C | T | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.33+1108C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957237 | ||||||
chr5:72957391
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.33+1262T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957391 | ||||||
chr5:72957392
|
G | T | 1 | a0001c0001t0001g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.33+1263G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957392 | ||||||
chr5:72957393
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.33+1264C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957393 | ||||||
chr5:72957766
|
T | C | 1 | a0001c0004t0003g0237 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.33+1637T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957766 | ||||||
chr5:72958237
|
A | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+2108A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958237 | ||||||
chr5:72958395
|
G | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+2266G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958395 | ||||||
chr5:72958398
|
A | G | 4 | a0002c0002t0002g0067a0002c0002t0002g0068a0002c0002t0002g0069others(1): Show | 4 | HG01243.hp2 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+2269A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958398 | ||||||
chr5:72958543
|
C | T | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.33+2414C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958543 | ||||||
chr5:72958778
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.33+2649T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958778 | ||||||
chr5:72958814
|
C | G | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33+2685C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958814 | ||||||
chr5:72959098
|
A | C | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.33+2969A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959098 | ||||||
chr5:72959138
|
T | C | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+3009T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959138 | ||||||
chr5:72959183
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33+3054A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959183 | ||||||
chr5:72959474
|
T | C | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.33+3345T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959474 | ||||||
chr5:72959646
|
T | G | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.33+3517T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959646 | ||||||
chr5:72959660
|
A | T | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.33+3531A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959660 | ||||||
chr5:72959779
|
CT | C | 8 | a0001c0001t0001g0119a0001c0003t0004g0071a0001c0003t0005g0002others(5): Show | 8 | HG00099.hp2 HG01099.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.33+3666delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72959779 | |||||
chr5:72959783
|
T | C | 116 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(113): Show | 116 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.33+3654T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959783 | ||||||
chr5:72959784
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.33+3655T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959784 | ||||||
chr5:72959847
|
A | G | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33+3718A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959847 | ||||||
chr5:72959981
|
T | C | 117 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(114): Show | 117 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.33+3852T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959981 | ||||||
chr5:72960026
|
C | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.33+3897C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960026 | ||||||
chr5:72960257
|
A | G | 1 | a0001c0001t0007g0231 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.33+4128A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960257 | ||||||
chr5:72960262
|
A | C | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+4133A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960262 | ||||||
chr5:72960311
|
G | GA | 214 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(211): Show | 214 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.33+4187dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72960311 | |||||
chr5:72960328
|
C | T | 44 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.33+4199C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960328 | ||||||
chr5:72960483
|
A | AAAC | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.33+4357_33+4359dup others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72960483 | |||||
chr5:72960488
|
A | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+4359A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960488 | ||||||
chr5:72960607
|
C | T | 97 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.33+4478C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960607 | ||||||
chr5:72960800
|
A | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+4671A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960800 | ||||||
chr5:72960804
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33+4675C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960804 | ||||||
chr5:72961353
|
G | T | 88 | a0001c0001t0001g0117a0001c0001t0001g0145a0001c0001t0001g0146others(85): Show | 88 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.33+5224G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961353 | ||||||
chr5:72961431
|
A | G | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.33+5302A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961431 | ||||||
chr5:72961541
|
T | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG01106.hp1 HG01123.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+5412T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961541 | ||||||
chr5:72961617
|
G | A | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33+5488G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961617 | ||||||
chr5:72961625
|
G | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33+5496G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961625 | ||||||
chr5:72961834
|
G | A | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.33+5705G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961834 | ||||||
chr5:72961887
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.33+5758G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961887 | ||||||
chr5:72961964
|
A | G | 4 | a0001c0001t0007g0228a0001c0001t0007g0229a0001c0001t0007g0230others(1): Show | 4 | HG01081.hp2 HG01496.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+5835A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961964 | ||||||
chr5:72962003
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.33+5874T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962003 | ||||||
chr5:72962630
|
C | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.34-5868C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962630 | ||||||
chr5:72962657
|
A | G | 3 | a0001c0003t0010g0009a0001c0003t0010g0010a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.34-5841A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962657 | ||||||
chr5:72962695
|
C | T | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.34-5803C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962695 | ||||||
chr5:72962696
|
C | T | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.34-5802C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962696 | ||||||
chr5:72962891
|
C | CA | 60 | a0001c0001t0001g0153a0001c0003t0003g0099a0001c0003t0003g0100others(57): Show | 60 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.34-5595dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72962891 | |||||
chr5:72963074
|
A | G | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.34-5424A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963074 | ||||||
chr5:72963086
|
T | G | 2 | a0001c0004t0003g0284a0001c0004t0003g0285 | 2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.34-5412T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963086 | ||||||
chr5:72963185
|
C | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-5313C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963185 | ||||||
chr5:72963600
|
T | TG | 3 | a0002c0002t0002g0064a0002c0002t0002g0065a0002c0002t0002g0066 | 3 | HG03471.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.34-4896dupG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963600 | |||||
chr5:72963622
|
C | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.34-4876C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963622 | ||||||
chr5:72963694
|
G | A | 2 | a0002c0002t0002g0011a0002c0002t0002g0012 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.34-4804G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963694 | ||||||
chr5:72963729
|
T | A | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.34-4769T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963729 | ||||||
chr5:72963902
|
G | GT | 9 | a0002c0002t0002g0056a0002c0002t0002g0057a0002c0002t0002g0058others(6): Show | 9 | HG01884.hp2 HG02027.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.34-4569dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | |||||
chr5:72963902
|
GT | G | 28 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(25): Show | 28 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-4569delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | |||||
chr5:72963902
|
GTT | G | 115 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 115 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.34-4570_34-4569del others(2): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | |||||
chr5:72963902
|
GTTT | G | 61 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0155others(58): Show | 61 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.34-4571_34-4569del others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | |||||
chr5:72963902
|
GTTTT | G | 7 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(4): Show | 7 | HG02145.hp2 HG02809.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-4572_34-4569del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | |||||
chr5:72963902
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.34-4578_34-4569del others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | |||||
chr5:72963906
|
T | G | 43 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(40): Show | 43 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.34-4592T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963906 | ||||||
chr5:72963907
|
T | G | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.34-4591T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963907 | ||||||
chr5:72963911
|
T | G | 1 | a0001c0003t0010g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.34-4587T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963911 | ||||||
chr5:72963912
|
T | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.34-4586T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963912 | ||||||
chr5:72963918
|
T | G | 44 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(41): Show | 44 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.34-4580T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963918 | ||||||
chr5:72963919
|
T | G | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.34-4579T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963919 | ||||||
chr5:72963926
|
T | G | 1 | a0002c0002t0002g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.34-4572T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963926 | ||||||
chr5:72963934
|
A | G | 12 | a0002c0002t0002g0050a0002c0002t0002g0051a0002c0002t0002g0052others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.34-4564A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963934 | ||||||
chr5:72964416
|
C | T | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.34-4082C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964416 | ||||||
chr5:72964454
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0216 | 2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.34-4044C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964454 | ||||||
chr5:72964619
|
C | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-3879C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964619 | ||||||
chr5:72964677
|
C | T | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.34-3821C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964677 | ||||||
chr5:72964742
|
C | G | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.34-3756C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964742 | ||||||
chr5:72965002
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.34-3496A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965002 | ||||||
chr5:72965136
|
A | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.34-3362A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965136 | ||||||
chr5:72965210
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.34-3288A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965210 | ||||||
chr5:72965230
|
T | C | 1 | a0001c0003t0008g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.34-3268T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965230 | ||||||
chr5:72965635
|
A | G | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.34-2863A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965635 | ||||||
chr5:72965703
|
T | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-2795T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965703 | ||||||
chr5:72965855
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.34-2643A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965855 | ||||||
chr5:72966199
|
G | A | 1 | a0002c0002t0002g0018 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.34-2299G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966199 | ||||||
chr5:72966386
|
G | A | 88 | a0001c0001t0001g0117a0001c0001t0001g0145a0001c0001t0001g0146others(85): Show | 88 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.34-2112G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966386 | ||||||
chr5:72966527
|
T | C | 1 | a0001c0001t0015g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.34-1971T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966527 | ||||||
chr5:72966655
|
T | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.34-1843T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966655 | ||||||
chr5:72966741
|
T | G | 5 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.34-1757T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966741 | ||||||
chr5:72967124
|
A | G | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.34-1374A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72967124 | ||||||
chr5:72967655
|
T | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.34-843T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72967655 | ||||||
chr5:72967700
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0224 | 3 | HG00735.hp2 HG01928.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.34-798A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72967700 | ||||||
chr5:72968003
|
C | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.34-495C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968003 | ||||||
chr5:72968053
|
T | G | 3 | a0001c0003t0004g0072a0001c0003t0004g0073a0001c0003t0004g0074 | 3 | HG01069.hp2 HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.34-445T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968053 | ||||||
chr5:72968081
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.34-417C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968081 | ||||||
chr5:72968114
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.34-384C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968114 | ||||||
chr5:72968296
|
T | C | 1 | a0001c0003t0004g0092 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.34-202T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968296 | ||||||
chr5:72968337
|
A | G | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.34-161A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968337 | ||||||
chr5:72968912
|
C | G | 2 | a0001c0003t0004g0091a0005c0011t0004g0090 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.125+323C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72968912 | ||||||
chr5:72969001
|
A | G | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125+412A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969001 | ||||||
chr5:72969146
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | NA18998.hp2 NA19001.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.125+557A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969146 | ||||||
chr5:72969272
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0215 | 2 | HG00597.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.125+683A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969272 | ||||||
chr5:72969340
|
T | A | 14 | a0001c0001t0001g0151a0001c0001t0001g0168a0001c0001t0001g0169others(11): Show | 14 | HG00735.hp2 HG01928.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.125+751T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969340 | ||||||
chr5:72970036
|
C | T | 6 | a0001c0004t0003g0271a0001c0004t0003g0272a0001c0004t0003g0273others(3): Show | 6 | HG02027.hp2 HG02071.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+1447C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970036 | ||||||
chr5:72970128
|
A | G | 1 | a0001c0004t0003g0276 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.125+1539A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970128 | ||||||
chr5:72970143
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.125+1554T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970143 | ||||||
chr5:72970149
|
A | G | 1 | a0002c0002t0002g0049 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.125+1560A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970149 | ||||||
chr5:72970473
|
CT | C | 8 | a0001c0001t0001g0216a0001c0003t0004g0093a0001c0004t0003g0237others(5): Show | 8 | HG00621.hp2 HG02523.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+1896delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72970473 | |||||
chr5:72970585
|
T | A | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.125+1996T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970585 | ||||||
chr5:72970680
|
C | A | 1 | a0002c0002t0002g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.125+2091C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970680 | ||||||
chr5:72970790
|
G | A | 1 | a0002c0002t0002g0114 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.125+2201G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970790 | ||||||
chr5:72970969
|
T | A | 1 | a0001c0001t0001g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.125+2380T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970969 | ||||||
chr5:72970969
|
T | C | 5 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.125+2380T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970969 | ||||||
chr5:72970978
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.125+2389A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970978 | ||||||
chr5:72970998
|
G | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+2409G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970998 | ||||||
chr5:72971052
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.125+2463A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971052 | ||||||
chr5:72971163
|
A | G | 4 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0047others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2574A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971163 | ||||||
chr5:72971165
|
A | G | 4 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0047others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2576A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971165 | ||||||
chr5:72971289
|
G | C | 1 | a0001c0003t0005g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.125+2700G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971289 | ||||||
chr5:72971345
|
C | T | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.125+2756C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971345 | ||||||
chr5:72972022
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0144 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.125+3433A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972022 | ||||||
chr5:72972075
|
G | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+3486G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972075 | ||||||
chr5:72972176
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.125+3587C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972176 | ||||||
chr5:72972177
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125+3588G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972177 | ||||||
chr5:72972378
|
G | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+3789G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972378 | ||||||
chr5:72972526
|
G | T | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+3937G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972526 | ||||||
chr5:72972610
|
A | G | 1 | a0001c0004t0003g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.125+4021A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972610 | ||||||
chr5:72972684
|
G | A | 98 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(95): Show | 98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.125+4095G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972684 | ||||||
chr5:72972703
|
T | C | 8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+4114T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972703 | ||||||
chr5:72972718
|
G | T | 45 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(42): Show | 45 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.125+4129G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972718 | ||||||
chr5:72972720
|
T | C | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.125+4131T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972720 | ||||||
chr5:72972810
|
C | T | 4 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+4221C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972810 | ||||||
chr5:72972842
|
C | T | 5 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(2): Show | 5 | HG00621.hp2 HG02523.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+4253C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972842 | ||||||
chr5:72972880
|
A | G | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.125+4291A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972880 | ||||||
chr5:72973053
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+4464C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973053 | ||||||
chr5:72973096
|
C | T | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.125+4507C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973096 | ||||||
chr5:72973185
|
C | T | 6 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+4596C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973185 | ||||||
chr5:72973186
|
A | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.125+4597A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973186 | ||||||
chr5:72973249
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+4660A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973249 | ||||||
chr5:72973293
|
G | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+4704G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973293 | ||||||
chr5:72973488
|
G | A | 3 | a0001c0001t0001g0166a0001c0003t0010g0009a0001c0003t0010g0010 | 3 | HG02615.hp1 HG02630.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.125+4899G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973488 | ||||||
chr5:72973532
|
TG | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0139a0001c0001t0001g0144 | 3 | HG02559.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.125+4946delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72973532 | |||||
chr5:72973538
|
C | T | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125+4949C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973538 | ||||||
chr5:72973572
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.125+4983G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973572 | ||||||
chr5:72973914
|
G | A | 7 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(4): Show | 7 | HG00438.hp1 NA18747.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.125+5325G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973914 | ||||||
chr5:72974191
|
T | C | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125+5602T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974191 | ||||||
chr5:72974241
|
C | G | 12 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(9): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+5652C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974241 | ||||||
chr5:72974275
|
G | A | 12 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(9): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+5686G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974275 | ||||||
chr5:72974283
|
T | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.125+5694T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974283 | ||||||
chr5:72974340
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.125+5751G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974340 | ||||||
chr5:72974448
|
T | C | 97 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.125+5859T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974448 | ||||||
chr5:72974490
|
T | A | 8 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+5901T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974490 | ||||||
chr5:72974604
|
T | C | 96 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.125+6015T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974604 | ||||||
chr5:72974620
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125+6031T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974620 | ||||||
chr5:72974683
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.125+6094G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974683 | ||||||
chr5:72974716
|
G | A | 3 | a0001c0003t0010g0009a0001c0003t0010g0010a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+6127G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974716 | ||||||
chr5:72974719
|
G | T | 50 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.125+6130G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974719 | ||||||
chr5:72974761
|
G | T | 5 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+6172G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974761 | ||||||
chr5:72974875
|
G | A | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.125+6286G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974875 | ||||||
chr5:72974885
|
G | T | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.125+6296G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974885 | ||||||
chr5:72974908
|
A | C | 2 | a0002c0002t0002g0045a0002c0002t0002g0046 | 2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.125+6319A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974908 | ||||||
chr5:72974955
|
A | G | 8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+6366A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974955 | ||||||
chr5:72974989
|
C | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+6400C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974989 | ||||||
chr5:72974990
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.125+6401G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974990 | ||||||
chr5:72974990
|
G | T | 5 | a0001c0003t0003g0277a0001c0003t0003g0278a0002c0002t0002g0016others(2): Show | 5 | HG00544.hp2 HG00597.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+6401G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974990 | ||||||
chr5:72975238
|
G | T | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+6649G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975238 | ||||||
chr5:72975429
|
C | T | 1 | a0001c0004t0003g0267 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.125+6840C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975429 | ||||||
chr5:72975470
|
C | T | 1 | a0001c0004t0003g0267 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.125+6881C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975470 | ||||||
chr5:72975487
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125+6898C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975487 | ||||||
chr5:72975568
|
G | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+6979G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975568 | ||||||
chr5:72975631
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125+7042A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975631 | ||||||
chr5:72975683
|
T | C | 5 | a0001c0003t0003g0279a0001c0003t0003g0281a0001c0003t0010g0009others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+7094T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975683 | ||||||
chr5:72975797
|
G | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+7208G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975797 | ||||||
chr5:72975900
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.125+7311A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975900 | ||||||
chr5:72975946
|
G | A | 1 | a0001c0003t0004g0098 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.125+7357G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975946 | ||||||
chr5:72976094
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02040.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.125+7505A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976094 | ||||||
chr5:72976119
|
C | T | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.125+7530C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976119 | ||||||
chr5:72976266
|
G | A | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.125+7677G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976266 | ||||||
chr5:72976285
|
C | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+7696C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976285 | ||||||
chr5:72976298
|
C | T | 10 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(7): Show | 10 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+7709C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976298 | ||||||
chr5:72976299
|
G | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+7710G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976299 | ||||||
chr5:72976519
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.125+7930C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976519 | ||||||
chr5:72976625
|
T | A | 2 | a0001c0003t0003g0277a0001c0003t0003g0278 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+8036T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976625 | ||||||
chr5:72976626
|
A | T | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125+8037A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976626 | ||||||
chr5:72976667
|
G | A | 53 | a0001c0003t0003g0277a0001c0003t0003g0278a0001c0003t0003g0279others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.125+8078G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976667 | ||||||
chr5:72976686
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+8097A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976686 | ||||||
chr5:72976713
|
G | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+8124G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976713 | ||||||
chr5:72976885
|
G | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+8296G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976885 | ||||||
chr5:72976976
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+8387G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976976 | ||||||
chr5:72977144
|
A | T | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+8555A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72977144 | ||||||
chr5:72977239
|
C | G | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+8650C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72977239 | ||||||
chr5:72977658
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125+9069A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72977658 | ||||||
chr5:72978001
|
A | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+9412A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978001 | ||||||
chr5:72978023
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.125+9434A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978023 | ||||||
chr5:72978209
|
A | G | 1 | a0002c0002t0002g0113 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.125+9620A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978209 | ||||||
chr5:72978299
|
A | G | 12 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(9): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+9710A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978299 | ||||||
chr5:72978891
|
G | T | 7 | a0001c0004t0003g0262a0001c0004t0003g0263a0001c0004t0003g0264others(4): Show | 7 | HG00558.hp2 HG00609.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.125+10302G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978891 | ||||||
chr5:72978897
|
G | A | 1 | a0001c0009t0001g0127 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.125+10308G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978897 | ||||||
chr5:72978923
|
G | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+10334G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978923 | ||||||
chr5:72978977
|
TA | T | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.125+10390delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72978977 | |||||
chr5:72979000
|
A | G | 12 | a0002c0002t0002g0050a0002c0002t0002g0051a0002c0002t0002g0052others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+10411A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979000 | ||||||
chr5:72979004
|
G | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+10415G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979004 | ||||||
chr5:72979319
|
C | T | 3 | a0001c0003t0010g0009a0001c0003t0010g0010a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-10108C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979319 | ||||||
chr5:72979354
|
A | G | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.126-10073A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979354 | ||||||
chr5:72979378
|
C | CT | 63 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.126-10018dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | |||||
chr5:72979378
|
C | CTT | 39 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0124others(36): Show | 39 | HG00438.hp1 HG00735.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-10019_126-1001 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | |||||
chr5:72979378
|
C | CTTT | 23 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0155others(20): Show | 23 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.126-10020_126-1001 others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | |||||
chr5:72979378
|
C | CTTTT | 10 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0001g0154others(7): Show | 10 | HG01258.hp2 HG01884.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.126-10021_126-1001 others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | |||||
chr5:72979378
|
CT | C | 48 | a0001c0003t0003g0099a0001c0003t0003g0277a0001c0003t0003g0278others(45): Show | 48 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.126-10018delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | |||||
chr5:72979378
|
CTT | C | 39 | a0001c0001t0015g0167a0001c0003t0004g0071a0001c0003t0004g0072others(36): Show | 39 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.126-10019_126-1001 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | |||||
chr5:72979378
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-10027_126-1001 others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | |||||
chr5:72979392
|
T | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-10035T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979392 | ||||||
chr5:72979393
|
T | C | 1 | a0001c0003t0005g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.126-10034T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979393 | ||||||
chr5:72979394
|
T | C | 1 | a0001c0003t0005g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-10033T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979394 | ||||||
chr5:72979442
|
A | G | 1 | a0001c0003t0010g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126-9985A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979442 | ||||||
chr5:72979452
|
C | T | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126-9975C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979452 | ||||||
chr5:72979455
|
G | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-9972G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979455 | ||||||
chr5:72979460
|
C | T | 50 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.126-9967C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979460 | ||||||
chr5:72979537
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126-9890G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979537 | ||||||
chr5:72979686
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.126-9741C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979686 | ||||||
chr5:72979733
|
G | A | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126-9694G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979733 | ||||||
chr5:72979777
|
G | T | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.126-9650G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979777 | ||||||
chr5:72979795
|
C | G | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.126-9632C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979795 | ||||||
chr5:72980190
|
C | A | 97 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.126-9237C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980190 | ||||||
chr5:72980272
|
T | A | 97 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.126-9155T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980272 | ||||||
chr5:72980684
|
C | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-8743C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980684 | ||||||
chr5:72980685
|
C | G | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.126-8742C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980685 | ||||||
chr5:72980711
|
C | T | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-8716C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980711 | ||||||
chr5:72980794
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126-8633T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980794 | ||||||
chr5:72980849
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-8578G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980849 | ||||||
chr5:72980946
|
T | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-8481T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980946 | ||||||
chr5:72981295
|
G | GT | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.126-8129dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72981295 | |||||
chr5:72981310
|
T | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0138 | 3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.126-8117T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981310 | ||||||
chr5:72981598
|
C | T | 1 | a0001c0004t0003g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.126-7829C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981598 | ||||||
chr5:72981599
|
G | A | 4 | a0001c0003t0004g0086a0001c0003t0004g0087a0001c0003t0004g0098others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-7828G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981599 | ||||||
chr5:72981627
|
G | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-7800G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981627 | ||||||
chr5:72981733
|
G | A | 46 | a0001c0003t0003g0279a0001c0003t0003g0281a0001c0004t0003g0237others(43): Show | 46 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.126-7694G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981733 | ||||||
chr5:72981742
|
A | G | 12 | a0002c0002t0002g0050a0002c0002t0002g0051a0002c0002t0002g0052others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-7685A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981742 | ||||||
chr5:72981809
|
T | C | 1 | a0005c0011t0004g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.126-7618T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981809 | ||||||
chr5:72981897
|
C | A | 117 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(114): Show | 117 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.126-7530C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981897 | ||||||
chr5:72981992
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.126-7435G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981992 | ||||||
chr5:72982040
|
G | A | 2 | a0002c0002t0002g0035a0002c0002t0002g0061 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.126-7387G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982040 | ||||||
chr5:72982069
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.126-7358C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982069 | ||||||
chr5:72982081
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126-7346A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982081 | ||||||
chr5:72982095
|
G | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-7332G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982095 | ||||||
chr5:72982127
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | NA18998.hp2 NA19001.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.126-7300C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982127 | ||||||
chr5:72982206
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.126-7221C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982206 | ||||||
chr5:72982332
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.126-7095G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982332 | ||||||
chr5:72982380
|
T | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-7047T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982380 | ||||||
chr5:72982723
|
T | C | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-6704T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982723 | ||||||
chr5:72982762
|
A | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.126-6665A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982762 | ||||||
chr5:72982822
|
A | T | 2 | a0002c0002t0002g0015a0002c0002t0002g0064 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.126-6605A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982822 | ||||||
chr5:72982826
|
AT | A | 18 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0140others(15): Show | 18 | HG00558.hp1 HG02074.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-6581delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72982826 | |||||
chr5:72982826
|
ATT | A | 197 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(194): Show | 197 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.126-6582_126-6581d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72982826 | |||||
chr5:72982931
|
TCAGA | T | 23 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(20): Show | 23 | HG00597.hp2 HG01070.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.126-6491_126-6488d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72982931 | |||||
chr5:72982974
|
C | T | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.126-6453C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982974 | ||||||
chr5:72983037
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0227 | 2 | HG01978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.126-6390C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983037 | ||||||
chr5:72983062
|
C | T | 3 | a0001c0003t0004g0081a0001c0003t0004g0095a0002c0002t0002g0060 | 3 | HG00423.hp1 HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.126-6365C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983062 | ||||||
chr5:72983080
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.126-6347A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983080 | ||||||
chr5:72983126
|
A | T | 1 | a0002c0002t0002g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.126-6301A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983126 | ||||||
chr5:72983209
|
C | G | 46 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0152others(43): Show | 46 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.126-6218C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983209 | ||||||
chr5:72983236
|
C | T | 1 | a0002c0002t0002g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126-6191C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983236 | ||||||
chr5:72983335
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.126-6092G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983335 | ||||||
chr5:72983336
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.126-6091G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983336 | ||||||
chr5:72983482
|
G | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-5945G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983482 | ||||||
chr5:72983547
|
C | CT | 12 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0177others(9): Show | 12 | HG01243.hp1 HG02074.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-5858dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72983547 | |||||
chr5:72983547
|
CT | C | 12 | a0001c0001t0001g0166a0001c0001t0001g0213a0001c0003t0004g0081others(9): Show | 12 | HG00423.hp1 HG00609.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-5858delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72983547 | |||||
chr5:72983704
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.126-5723C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983704 | ||||||
chr5:72983733
|
A | C | 6 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-5694A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983733 | ||||||
chr5:72983810
|
T | A | 3 | a0001c0003t0010g0009a0001c0003t0010g0010a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-5617T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983810 | ||||||
chr5:72983886
|
A | G | 1 | a0001c0003t0003g0278 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126-5541A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983886 | ||||||
chr5:72983990
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.126-5437A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983990 | ||||||
chr5:72984117
|
T | G | 2 | a0002c0002t0002g0001a0002c0002t0002g0022 | 3 | HG01070.hp2 HG01071.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.126-5310T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984117 | ||||||
chr5:72984210
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126-5217C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984210 | ||||||
chr5:72984348
|
CT | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-5078delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984348 | ||||||
chr5:72984521
|
A | G | 5 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-4906A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984521 | ||||||
chr5:72984577
|
A | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-4850A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984577 | ||||||
chr5:72984937
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.126-4490A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984937 | ||||||
chr5:72985258
|
T | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0138 | 3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.126-4169T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985258 | ||||||
chr5:72985286
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126-4141C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985286 | ||||||
chr5:72985287
|
G | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.126-4140G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985287 | ||||||
chr5:72985488
|
T | A | 115 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(112): Show | 115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.126-3939T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985488 | ||||||
chr5:72985902
|
T | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.126-3525T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985902 | ||||||
chr5:72986131
|
A | T | 8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-3296A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986131 | ||||||
chr5:72986240
|
AT | A | 213 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(210): Show | 213 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.126-3177delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72986240 | |||||
chr5:72986254
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.126-3173T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986254 | ||||||
chr5:72986259
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-3168C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986259 | ||||||
chr5:72986347
|
A | G | 1 | a0002c0002t0002g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126-3080A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986347 | ||||||
chr5:72986418
|
A | G | 4 | a0001c0003t0004g0086a0001c0003t0004g0087a0001c0003t0004g0098others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-3009A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986418 | ||||||
chr5:72986626
|
A | T | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126-2801A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986626 | ||||||
chr5:72986640
|
A | G | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.126-2787A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986640 | ||||||
chr5:72986823
|
A | G | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.126-2604A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986823 | ||||||
chr5:72986885
|
C | CT | 10 | a0001c0001t0001g0175a0001c0004t0003g0260a0002c0002t0002g0050others(7): Show | 10 | HG01884.hp2 HG02809.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-2530dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72986885 | |||||
chr5:72987153
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-2274G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987153 | ||||||
chr5:72987171
|
C | T | 1 | a0002c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.126-2256C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987171 | ||||||
chr5:72987412
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-2015A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987412 | ||||||
chr5:72987460
|
T | C | 16 | a0001c0003t0005g0002a0001c0003t0005g0105a0001c0003t0005g0106others(13): Show | 16 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-1967T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987460 | ||||||
chr5:72987628
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0198 | 2 | NA18947.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.126-1799G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987628 | ||||||
chr5:72988109
|
C | G | 11 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(8): Show | 11 | HG00642.hp2 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.126-1318C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988109 | ||||||
chr5:72988166
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.126-1261G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988166 | ||||||
chr5:72988392
|
T | C | 217 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(214): Show | 217 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.126-1035T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988392 | ||||||
chr5:72988393
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.126-1034G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988393 | ||||||
chr5:72988742
|
A | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-685A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988742 | ||||||
chr5:72988776
|
GAATT | G | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-649_126-646del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72988776 | |||||
chr5:72988791
|
A | G | 5 | a0001c0004t0003g0271a0001c0004t0003g0272a0001c0004t0003g0273others(2): Show | 5 | HG02027.hp2 HG02071.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-636A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988791 | ||||||
chr5:72988856
|
G | T | 1 | a0001c0001t0007g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.126-571G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988856 | ||||||
chr5:72988986
|
A | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.126-441A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988986 | ||||||
chr5:72989012
|
T | C | 14 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(11): Show | 14 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.126-415T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72989012 | ||||||
chr5:72989026
|
T | G | 4 | a0002c0002t0002g0036a0002c0002t0002g0045a0002c0002t0002g0046others(1): Show | 4 | NA18964.hp2 NA18994.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-401T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72989026 | ||||||
chr5:72989339
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.126-88G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72989339 | ||||||
chr5:72989594
|
T | C | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.200+93T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989594 | ||||||
chr5:72989705
|
A | C | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.200+204A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989705 | ||||||
chr5:72989880
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.200+379T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989880 | ||||||
chr5:72989921
|
T | C | 4 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.200+420T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989921 | ||||||
chr5:72990057
|
G | C | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.201-421G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72990057 | ||||||
chr5:72990159
|
TAG | T | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.201-317_201-316del others(2): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 72990159 | |||||
chr5:72990387
|
A | G | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.201-91A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72990387 | ||||||
chr5:72990657
|
G | C | 3 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103 | 3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.342+38G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 4/25 | chr5 | 72990657 | ||||||
chr5:72991126
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+262G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991126 | ||||||
chr5:72991153
|
C | G | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.495+289C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991153 | ||||||
chr5:72991220
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+356A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991220 | ||||||
chr5:72991250
|
G | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+386G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991250 | ||||||
chr5:72991280
|
T | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+416T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991280 | ||||||
chr5:72991341
|
G | C | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(3): Show | 6 | HG00597.hp2 HG02040.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+477G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991341 | ||||||
chr5:72991353
|
T | C | 5 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+489T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991353 | ||||||
chr5:72991444
|
G | A | 1 | a0001c0004t0003g0271 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.495+580G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991444 | ||||||
chr5:72991801
|
A | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+937A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991801 | ||||||
chr5:72992903
|
T | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+2039T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72992903 | ||||||
chr5:72992903
|
T | G | 4 | a0002c0002t0002g0036a0002c0002t0002g0045a0002c0002t0002g0046others(1): Show | 4 | NA18964.hp2 NA18994.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+2039T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72992903 | ||||||
chr5:72992965
|
TA | T | 53 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.495+2113delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72992965 | |||||
chr5:72992986
|
C | T | 1 | a0002c0002t0002g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.495+2122C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72992986 | ||||||
chr5:72993264
|
T | G | 1 | a0001c0004t0003g0242 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.495+2400T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993264 | ||||||
chr5:72993591
|
C | A | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.495+2727C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993591 | ||||||
chr5:72993694
|
G | A | 50 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.495+2830G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993694 | ||||||
chr5:72993780
|
T | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+2916T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993780 | ||||||
chr5:72993844
|
G | T | 214 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(211): Show | 214 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.495+2980G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993844 | ||||||
chr5:72993902
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.495+3038A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993902 | ||||||
chr5:72994024
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+3160A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994024 | ||||||
chr5:72994078
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.495+3214A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994078 | ||||||
chr5:72994155
|
T | A | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.495+3291T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994155 | ||||||
chr5:72994265
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+3401A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994265 | ||||||
chr5:72994316
|
G | A | 2 | a0001c0003t0004g0084a0001c0003t0004g0085 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.495+3452G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994316 | ||||||
chr5:72994508
|
G | A | 1 | a0001c0004t0003g0259 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.495+3644G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994508 | ||||||
chr5:72994559
|
G | A | 6 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0018others(3): Show | 6 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+3695G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994559 | ||||||
chr5:72994617
|
C | A | 1 | a0001c0003t0003g0278 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.495+3753C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994617 | ||||||
chr5:72994621
|
C | A | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3757C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994621 | ||||||
chr5:72994634
|
A | G | 1 | a0001c0001t0018g0226 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.495+3770A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994634 | ||||||
chr5:72994696
|
A | T | 1 | a0001c0005t0003g0258 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.495+3832A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994696 | ||||||
chr5:72994800
|
A | G | 3 | a0001c0003t0010g0009a0001c0003t0010g0010a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+3936A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994800 | ||||||
chr5:72994830
|
G | A | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3966G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994830 | ||||||
chr5:72994922
|
T | G | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+4058T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994922 | ||||||
chr5:72995004
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.495+4140C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995004 | ||||||
chr5:72995125
|
A | G | 1 | a0001c0001t0007g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.495+4261A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995125 | ||||||
chr5:72995173
|
GAAAT | G | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.495+4312_495+4315d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72995173 | |||||
chr5:72995351
|
G | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+4487G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995351 | ||||||
chr5:72995380
|
C | T | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.495+4516C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995380 | ||||||
chr5:72995629
|
A | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+4765A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995629 | ||||||
chr5:72995640
|
G | A | 2 | a0001c0003t0011g0232a0003c0006t0005g0003 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.495+4776G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995640 | ||||||
chr5:72995658
|
G | C | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.495+4794G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995658 | ||||||
chr5:72995703
|
G | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+4839G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995703 | ||||||
chr5:72995868
|
C | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+5004C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995868 | ||||||
chr5:72995932
|
A | G | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.495+5068A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995932 | ||||||
chr5:72996230
|
C | T | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.495+5366C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996230 | ||||||
chr5:72996241
|
C | T | 1 | a0001c0004t0003g0237 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.495+5377C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996241 | ||||||
chr5:72996243
|
C | A | 1 | a0001c0004t0003g0237 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.495+5379C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996243 | ||||||
chr5:72996243
|
C | CA | 71 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0123others(68): Show | 71 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.495+5396dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996243
|
C | CAAAAAAA | 13 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(10): Show | 13 | HG00558.hp2 HG00609.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+5390_495+5396d others(9): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996243
|
C | CAAAAAAA others(1): Show |
37 | a0001c0003t0003g0281a0001c0003t0005g0002a0001c0003t0005g0106others(34): Show | 37 | HG00621.hp2 HG01081.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.495+5389_495+5396d others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996243
|
C | CAAAAAAA others(2): Show |
13 | a0001c0003t0005g0105a0001c0003t0005g0107a0001c0003t0005g0235others(10): Show | 13 | HG00735.hp1 HG02109.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+5388_495+5396d others(11): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996243
|
C | CAAAAAAA others(3): Show |
28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+5387_495+5396d others(12): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996243
|
C | CAAAAAAA others(4): Show |
4 | a0001c0003t0004g0081a0001c0003t0004g0094a0001c0003t0005g0108others(1): Show | 4 | HG00609.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+5386_495+5396d others(13): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996243
|
C | CAAAAAAA others(5): Show |
1 | a0001c0003t0016g0097 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.495+5385_495+5396d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996243
|
C | CAAAAAAA others(6): Show |
1 | a0001c0003t0010g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.495+5384_495+5396d others(15): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | |||||
chr5:72996439
|
A | C | 1 | a0001c0003t0008g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+5575A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996439 | ||||||
chr5:72996611
|
G | A | 3 | a0001c0001t0001g0184a0001c0003t0005g0234a0001c0003t0005g0235 | 3 | HG02622.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.495+5747G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996611 | ||||||
chr5:72996726
|
C | T | 2 | a0002c0002t0002g0035a0002c0002t0002g0061 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.495+5862C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996726 | ||||||
chr5:72996805
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+5941C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996805 | ||||||
chr5:72996847
|
C | T | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+5983C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996847 | ||||||
chr5:72996883
|
C | T | 30 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0003t0004g0071others(27): Show | 30 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.495+6019C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996883 | ||||||
chr5:72997279
|
G | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+6415G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997279 | ||||||
chr5:72997315
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG03017.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.495+6451G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997315 | ||||||
chr5:72997573
|
G | T | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.495+6709G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997573 | ||||||
chr5:72997574
|
G | T | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.495+6710G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997574 | ||||||
chr5:72997785
|
A | G | 3 | a0002c0002t0002g0041a0002c0002t0002g0065a0002c0002t0002g0066 | 3 | HG02559.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.495+6921A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997785 | ||||||
chr5:72997850
|
C | T | 1 | a0002c0002t0002g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.495+6986C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997850 | ||||||
chr5:72998213
|
C | T | 2 | a0002c0002t0002g0015a0002c0002t0002g0064 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.495+7349C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998213 | ||||||
chr5:72998343
|
C | T | 40 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(37): Show | 40 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.495+7479C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998343 | ||||||
chr5:72998345
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+7481G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998345 | ||||||
chr5:72998466
|
A | C | 1 | a0001c0003t0008g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+7602A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998466 | ||||||
chr5:72998631
|
A | G | 164 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.495+7767A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998631 | ||||||
chr5:72998815
|
A | G | 1 | a0001c0009t0001g0127 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.496-7630A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998815 | ||||||
chr5:72998887
|
G | A | 1 | a0002c0002t0002g0013 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.496-7558G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998887 | ||||||
chr5:72999241
|
C | T | 51 | a0001c0001t0001g0192a0001c0003t0003g0099a0001c0003t0003g0100others(48): Show | 51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.496-7204C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999241 | ||||||
chr5:72999277
|
T | A | 1 | a0002c0002t0002g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496-7168T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999277 | ||||||
chr5:72999329
|
T | C | 2 | a0001c0003t0003g0277a0001c0003t0003g0278 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.496-7116T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999329 | ||||||
chr5:72999378
|
C | CT | 8 | a0001c0001t0001g0131a0001c0001t0001g0177a0001c0001t0001g0192others(5): Show | 8 | HG01261.hp2 HG02615.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-7045dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999378 | |||||
chr5:72999378
|
CT | C | 33 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0194others(30): Show | 33 | HG01081.hp2 HG01169.hp2 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.496-7045delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999378 | |||||
chr5:72999378
|
CTT | C | 104 | a0001c0003t0003g0099a0001c0003t0003g0277a0001c0003t0003g0279others(101): Show | 105 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.496-7046_496-7045d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999378 | |||||
chr5:72999531
|
C | T | 7 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.496-6914C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999531 | ||||||
chr5:72999623
|
T | TA | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-6821dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999623 | |||||
chr5:72999630
|
G | A | 1 | a0002c0002t0002g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.496-6815G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999630 | ||||||
chr5:72999680
|
C | A | 1 | a0002c0002t0002g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.496-6765C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999680 | ||||||
chr5:72999709
|
C | CT | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-6734dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999709 | |||||
chr5:72999717
|
G | A | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-6728G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999717 | ||||||
chr5:72999750
|
C | T | 92 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(89): Show | 92 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.496-6695C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999750 | ||||||
chr5:72999799
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-6646G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999799 | ||||||
chr5:72999808
|
A | G | 3 | a0001c0003t0010g0009a0001c0003t0010g0010a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-6637A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999808 | ||||||
chr5:72999835
|
A | G | 1 | a0002c0002t0002g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.496-6610A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999835 | ||||||
chr5:72999881
|
G | C | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.496-6564G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999881 | ||||||
chr5:72999932
|
G | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-6513G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999932 | ||||||
chr5:73000183
|
A | T | 1 | a0002c0002t0002g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496-6262A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000183 | ||||||
chr5:73000189
|
C | T | 3 | a0001c0003t0010g0009a0001c0003t0010g0010a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-6256C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000189 | ||||||
chr5:73000458
|
T | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-5987T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000458 | ||||||
chr5:73000471
|
T | TA | 16 | a0001c0001t0001g0164a0001c0001t0001g0178a0001c0001t0001g0189others(13): Show | 16 | HG00438.hp1 HG00597.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-5951dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000471 | |||||
chr5:73000471
|
TA | T | 50 | a0001c0001t0001g0161a0001c0003t0003g0100a0001c0003t0003g0277others(47): Show | 50 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.496-5951delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000471 | |||||
chr5:73000471
|
TAA | T | 42 | a0001c0003t0003g0279a0001c0003t0003g0281a0001c0004t0003g0237others(39): Show | 42 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.496-5952_496-5951d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000471 | |||||
chr5:73000546
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.496-5899C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000546 | ||||||
chr5:73000558
|
T | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.496-5887T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000558 | ||||||
chr5:73000779
|
T | TA | 170 | a0001c0001t0001g0168a0001c0003t0003g0099a0001c0003t0003g0100others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.496-5656dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000779 | |||||
chr5:73001133
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.496-5312A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001133 | ||||||
chr5:73001202
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-5243G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001202 | ||||||
chr5:73001245
|
A | T | 3 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103 | 3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.496-5200A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001245 | ||||||
chr5:73001448
|
C | CA | 10 | a0001c0001t0001g0131a0001c0001t0001g0168a0001c0001t0001g0214others(7): Show | 10 | HG00735.hp2 HG02027.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.496-4974dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73001448 | |||||
chr5:73001448
|
CA | C | 91 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0201others(88): Show | 91 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.496-4974delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73001448 | |||||
chr5:73001467
|
A | G | 1 | a0002c0002t0002g0038 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.496-4978A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001467 | ||||||
chr5:73001674
|
G | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-4771G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001674 | ||||||
chr5:73001798
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.496-4647G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001798 | ||||||
chr5:73001943
|
T | A | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.496-4502T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001943 | ||||||
chr5:73002083
|
G | T | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.496-4362G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002083 | ||||||
chr5:73002255
|
G | T | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.496-4190G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002255 | ||||||
chr5:73002306
|
A | G | 5 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-4139A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002306 | ||||||
chr5:73002429
|
A | C | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.496-4016A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002429 | ||||||
chr5:73002802
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.496-3643G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002802 | ||||||
chr5:73002951
|
A | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-3494A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002951 | ||||||
chr5:73003086
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0216 | 2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.496-3359C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003086 | ||||||
chr5:73003117
|
A | T | 1 | a0002c0002t0002g0022 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.496-3328A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003117 | ||||||
chr5:73003212
|
C | T | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.496-3233C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003212 | ||||||
chr5:73003358
|
G | C | 8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.496-3087G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003358 | ||||||
chr5:73003425
|
G | C | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-3020G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003425 | ||||||
chr5:73003520
|
G | T | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.496-2925G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003520 | ||||||
chr5:73003908
|
C | T | 1 | a0002c0002t0002g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.496-2537C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003908 | ||||||
chr5:73003920
|
C | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-2525C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003920 | ||||||
chr5:73003949
|
G | A | 4 | a0002c0002t0002g0113a0002c0002t0002g0114a0002c0002t0002g0115others(1): Show | 4 | HG01928.hp2 HG02300.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-2496G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003949 | ||||||
chr5:73004047
|
C | CA | 38 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0145others(35): Show | 39 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.496-2372dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73004047 | |||||
chr5:73004047
|
CA | C | 9 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0209others(6): Show | 9 | HG00099.hp2 HG00558.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.496-2372delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73004047 | |||||
chr5:73004096
|
C | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.496-2349C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004096 | ||||||
chr5:73004393
|
A | G | 1 | a0001c0003t0006g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.496-2052A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004393 | ||||||
chr5:73004399
|
G | C | 1 | a0002c0002t0002g0016 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.496-2046G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004399 | ||||||
chr5:73004636
|
T | A | 110 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.496-1809T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004636 | ||||||
chr5:73004636
|
T | TA | 48 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(45): Show | 48 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.496-1801dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73004636 | |||||
chr5:73005091
|
C | T | 1 | a0002c0002t0002g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496-1354C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005091 | ||||||
chr5:73005198
|
A | G | 1 | a0001c0003t0004g0082 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.496-1247A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005198 | ||||||
chr5:73005710
|
T | A | 1 | a0001c0003t0003g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-735T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005710 | ||||||
chr5:73005874
|
G | A | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(3): Show | 6 | HG00597.hp2 HG02040.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-571G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005874 | ||||||
chr5:73005877
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.496-568A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005877 | ||||||
chr5:73006106
|
TTC | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-334_496-333del others(2): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73006106 | |||||
chr5:73006409
|
G | T | 6 | a0001c0004t0003g0241a0001c0004t0003g0247a0001c0004t0003g0249others(3): Show | 6 | NA18940.hp2 NA18941.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-36G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73006409 | ||||||
chr5:73006583
|
G | C | 3 | a0001c0004t0003g0242a0001c0004t0003g0284a0001c0004t0003g0285 | 3 | NA18982.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.600+34G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006583 | ||||||
chr5:73006603
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.600+54T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006603 | ||||||
chr5:73006697
|
G | T | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.600+148G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006697 | ||||||
chr5:73006922
|
A | G | 1 | a0001c0004t0003g0273 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.600+373A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006922 | ||||||
chr5:73006945
|
A | G | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+396A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006945 | ||||||
chr5:73007189
|
C | A | 1 | a0001c0001t0001g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.600+640C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007189 | ||||||
chr5:73007302
|
G | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+753G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007302 | ||||||
chr5:73007698
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.600+1149A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007698 | ||||||
chr5:73007717
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.600+1168A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007717 | ||||||
chr5:73007961
|
A | T | 70 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(67): Show | 71 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.600+1412A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007961 | ||||||
chr5:73008241
|
G | T | 5 | a0001c0005t0003g0248a0001c0005t0003g0254a0001c0005t0003g0257others(2): Show | 5 | NA18939.hp1 NA18966.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+1692G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008241 | ||||||
chr5:73008318
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.600+1769A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008318 | ||||||
chr5:73008650
|
A | G | 1 | a0001c0004t0003g0276 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.600+2101A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008650 | ||||||
chr5:73008984
|
A | T | 4 | a0001c0003t0004g0078a0001c0003t0004g0079a0001c0003t0004g0083others(1): Show | 4 | HG00438.hp2 NA18984.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+2435A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008984 | ||||||
chr5:73008990
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.600+2441G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008990 | ||||||
chr5:73009093
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.600+2544A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009093 | ||||||
chr5:73009115
|
G | A | 14 | a0001c0001t0001g0151a0001c0001t0001g0168a0001c0001t0001g0169others(11): Show | 14 | HG00735.hp2 HG01928.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+2566G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009115 | ||||||
chr5:73009273
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+2724C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009273 | ||||||
chr5:73009376
|
C | T | 166 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.600+2827C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009376 | ||||||
chr5:73009710
|
T | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.600+3161T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009710 | ||||||
chr5:73009780
|
G | C | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.600+3231G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009780 | ||||||
chr5:73010019
|
A | C | 79 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(76): Show | 80 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.600+3470A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010019 | ||||||
chr5:73010407
|
T | C | 1 | a0001c0003t0005g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.600+3858T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010407 | ||||||
chr5:73010626
|
C | T | 10 | a0002c0002t0002g0016a0002c0002t0002g0017a0002c0002t0002g0019others(7): Show | 10 | HG00544.hp2 HG00597.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+4077C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010626 | ||||||
chr5:73010746
|
G | A | 1 | a0001c0001t0015g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.600+4197G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010746 | ||||||
chr5:73010875
|
C | CA | 52 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0147others(49): Show | 52 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.600+4353dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | |||||
chr5:73010875
|
CA | C | 10 | a0001c0001t0001g0166a0001c0001t0001g0205a0001c0001t0001g0213others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+4353delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | |||||
chr5:73010875
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0005g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.600+4344_600+4353d others(12): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | |||||
chr5:73010875
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0005g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+4343_600+4353d others(13): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | |||||
chr5:73010875
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0007g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.600+4342_600+4353d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | |||||
chr5:73010875
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+4341_600+4353d others(15): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | |||||
chr5:73011049
|
T | G | 1 | a0002c0002t0002g0049 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.600+4500T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011049 | ||||||
chr5:73011114
|
A | C | 1 | a0002c0002t0002g0004 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.601-4512A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011114 | ||||||
chr5:73011167
|
A | G | 1 | a0001c0004t0003g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.601-4459A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011167 | ||||||
chr5:73011242
|
G | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-4384G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011242 | ||||||
chr5:73011315
|
G | T | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.601-4311G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011315 | ||||||
chr5:73011461
|
A | AT | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.601-4156dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73011461 | |||||
chr5:73011488
|
T | C | 1 | a0001c0003t0004g0083 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.601-4138T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011488 | ||||||
chr5:73011500
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.601-4126A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011500 | ||||||
chr5:73011523
|
A | T | 1 | a0001c0001t0007g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.601-4103A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011523 | ||||||
chr5:73011802
|
G | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.601-3824G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011802 | ||||||
chr5:73011867
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.601-3759G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011867 | ||||||
chr5:73011896
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-3730C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011896 | ||||||
chr5:73011938
|
G | T | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.601-3688G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011938 | ||||||
chr5:73012164
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.601-3462T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012164 | ||||||
chr5:73012195
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.601-3431C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012195 | ||||||
chr5:73012204
|
A | G | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-3422A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012204 | ||||||
chr5:73012316
|
T | C | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.601-3310T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012316 | ||||||
chr5:73012334
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.601-3292T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012334 | ||||||
chr5:73012360
|
C | T | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.601-3266C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012360 | ||||||
chr5:73012617
|
C | CA | 10 | a0001c0001t0001g0126a0001c0001t0001g0139a0001c0001t0001g0176others(7): Show | 10 | HG00597.hp2 HG01168.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-2988dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73012617 | |||||
chr5:73012617
|
CA | C | 150 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.601-2988delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73012617 | |||||
chr5:73012713
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.601-2913A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012713 | ||||||
chr5:73012925
|
T | C | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.601-2701T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012925 | ||||||
chr5:73013066
|
T | A | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.601-2560T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013066 | ||||||
chr5:73013213
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.601-2413T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013213 | ||||||
chr5:73013236
|
C | T | 1 | a0001c0004t0003g0263 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.601-2390C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013236 | ||||||
chr5:73013300
|
G | C | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.601-2326G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013300 | ||||||
chr5:73013591
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.601-2035G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013591 | ||||||
chr5:73013658
|
T | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-1968T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013658 | ||||||
chr5:73013670
|
C | G | 1 | a0001c0003t0006g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.601-1956C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013670 | ||||||
chr5:73013681
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0130 | 2 | HG00558.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.601-1945T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013681 | ||||||
chr5:73013844
|
C | G | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.601-1782C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013844 | ||||||
chr5:73013858
|
G | C | 1 | a0002c0002t0002g0017 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.601-1768G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013858 | ||||||
chr5:73013928
|
C | CTGGCCT | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.601-1697_601-1692d others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73013928 | |||||
chr5:73013935
|
C | T | 1 | a0002c0002t0002g0113 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.601-1691C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013935 | ||||||
chr5:73014098
|
C | T | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.601-1528C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014098 | ||||||
chr5:73014149
|
G | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.601-1477G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014149 | ||||||
chr5:73014159
|
G | A | 1 | a0001c0004t0003g0274 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.601-1467G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014159 | ||||||
chr5:73014258
|
T | C | 1 | a0001c0003t0004g0076 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601-1368T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014258 | ||||||
chr5:73014287
|
C | T | 49 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(46): Show | 49 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.601-1339C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014287 | ||||||
chr5:73014322
|
T | C | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-1304T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014322 | ||||||
chr5:73014446
|
G | A | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.601-1180G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014446 | ||||||
chr5:73014575
|
A | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-1051A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014575 | ||||||
chr5:73014630
|
A | G | 1 | a0002c0002t0002g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.601-996A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014630 | ||||||
chr5:73014763
|
G | A | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-863G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014763 | ||||||
chr5:73014934
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.601-692A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014934 | ||||||
chr5:73015071
|
G | A | 4 | a0001c0004t0003g0252a0002c0002t0002g0015a0002c0002t0002g0021others(1): Show | 4 | HG02109.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-555G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73015071 | ||||||
chr5:73015075
|
C | CA | 35 | a0001c0001t0001g0131a0001c0001t0001g0140a0001c0001t0001g0147others(32): Show | 35 | HG00735.hp2 HG01069.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.601-529dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73015075 | |||||
chr5:73015075
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0003g0237 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.601-539_601-529del others(11): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73015075 | |||||
chr5:73015231
|
G | GGTGTGTA others(3): Show |
1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601-393_601-392ins others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73015231 | |||||
chr5:73015323
|
C | T | 1 | a0001c0004t0003g0263 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.601-303C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73015323 | ||||||
chr5:73015465
|
G | A | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-161G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73015465 | ||||||
chr5:73015771
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.699+47A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73015771 | ||||||
chr5:73015953
|
A | T | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.699+229A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73015953 | ||||||
chr5:73016292
|
TTTAAAAA others(21): Show |
T | 73 | a0001c0001t0001g0153a0001c0001t0001g0183a0001c0003t0003g0277others(70): Show | 74 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.699+605_699+632del others(28): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016292 | |||||
chr5:73016301
|
T | TATTTTAA others(133): Show |
1 | a0002c0002t0002g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.699+604_699+605ins others(140): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016301 | |||||
chr5:73016311
|
TGTTTAAA others(189): Show |
T | 2 | a0001c0004t0003g0244a0001c0004t0003g0250 | 2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.699+605_700-688del | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016311 | |||||
chr5:73016329
|
T | G | 8 | a0001c0001t0001g0184a0001c0001t0001g0188a0001c0001t0001g0218others(5): Show | 8 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.699+605T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016329 | ||||||
chr5:73016329
|
T | TATTTTAA others(21): Show |
1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.700-733_700-706dup others(28): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016329 | |||||
chr5:73016329
|
T | TATTTTAA others(77): Show |
1 | a0001c0001t0001g0208 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.699+699_700-706dup others(84): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016329 | |||||
chr5:73016357
|
G | T | 37 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0004g0071others(34): Show | 37 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.699+633G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016357 | ||||||
chr5:73016367
|
TGTTTAAA others(133): Show |
T | 1 | a0001c0001t0001g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.700-705_700-566del | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016367 | |||||
chr5:73016385
|
G | T | 3 | a0001c0003t0004g0092a0001c0003t0010g0009a0001c0003t0010g0010 | 3 | HG02615.hp1 HG02630.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.699+661G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016385 | ||||||
chr5:73016395
|
TGTTTAAA others(105): Show |
T | 3 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0011g0232 | 3 | HG02280.hp2 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.700-705_700-594del | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016395 | |||||
chr5:73016413
|
G | T | 4 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0010g0009others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+689G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016413 | ||||||
chr5:73016423
|
TGTTTAAA others(77): Show |
T | 8 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0008g0110others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.700-705_700-622del others(84): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016423 | |||||
chr5:73016451
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.699+727T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016451 | ||||||
chr5:73016451
|
TGTTTAAA others(49): Show |
T | 60 | a0001c0003t0003g0277a0001c0003t0003g0278a0001c0003t0003g0279others(57): Show | 60 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.700-705_700-650del others(56): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016451 | |||||
chr5:73016479
|
TGTTTAAA others(21): Show |
T | 21 | a0001c0001t0001g0130a0001c0001t0001g0159a0001c0001t0001g0160others(18): Show | 21 | HG00621.hp1 HG01069.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.700-705_700-678del others(28): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016479 | |||||
chr5:73016507
|
A | T | 166 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.700-705A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016507 | ||||||
chr5:73016525
|
G | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.700-687G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016525 | ||||||
chr5:73017000
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.700-212G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73017000 | ||||||
chr5:73017204
|
T | C | 1 | a0001c0003t0006g0104 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.700-8T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73017204 | ||||||
chr5:73017852
|
TG | T | 4 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0047others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+546delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73017852 | |||||
chr5:73018006
|
CTATT | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG00642.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+703_796+706del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73018006 | |||||
chr5:73018041
|
T | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.796+733T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018041 | ||||||
chr5:73018047
|
T | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+739T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018047 | ||||||
chr5:73018063
|
A | T | 41 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(38): Show | 41 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.796+755A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018063 | ||||||
chr5:73018298
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.796+990C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018298 | ||||||
chr5:73018299
|
C | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.796+991C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018299 | ||||||
chr5:73018394
|
A | G | 1 | a0001c0004t0003g0274 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.796+1086A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018394 | ||||||
chr5:73018436
|
C | CT | 33 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(30): Show | 33 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.796+1128_796+1129i others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018436 | ||||||
chr5:73018491
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.796+1183C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018491 | ||||||
chr5:73018526
|
T | C | 1 | a0001c0003t0004g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.796+1218T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018526 | ||||||
chr5:73019132
|
A | G | 6 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0018others(3): Show | 6 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.796+1824A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019132 | ||||||
chr5:73019486
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.796+2178A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019486 | ||||||
chr5:73019501
|
A | G | 7 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0003t0005g0105others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+2193A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019501 | ||||||
chr5:73019623
|
C | T | 4 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+2315C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019623 | ||||||
chr5:73019663
|
C | T | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.796+2355C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019663 | ||||||
chr5:73019784
|
C | G | 1 | a0001c0004t0003g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.796+2476C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019784 | ||||||
chr5:73019870
|
G | T | 1 | a0001c0004t0003g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.796+2562G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019870 | ||||||
chr5:73019963
|
A | G | 14 | a0001c0001t0001g0151a0001c0001t0001g0168a0001c0001t0001g0169others(11): Show | 14 | HG00735.hp2 HG01928.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.796+2655A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019963 | ||||||
chr5:73020031
|
A | G | 44 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0003t0004g0071others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.796+2723A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020031 | ||||||
chr5:73020274
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.796+2966A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020274 | ||||||
chr5:73020473
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.796+3165C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020473 | ||||||
chr5:73020610
|
G | A | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.796+3302G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020610 | ||||||
chr5:73020774
|
T | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+3466T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020774 | ||||||
chr5:73020975
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.796+3667C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020975 | ||||||
chr5:73021092
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+3784G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021092 | ||||||
chr5:73021326
|
C | T | 1 | a0001c0003t0006g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.796+4018C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021326 | ||||||
chr5:73021410
|
A | G | 3 | a0002c0002t0002g0033a0002c0002t0002g0037a0002c0002t0002g0059 | 3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.796+4102A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021410 | ||||||
chr5:73021647
|
A | G | 2 | a0001c0003t0004g0081a0001c0003t0004g0095 | 2 | HG00423.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.796+4339A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021647 | ||||||
chr5:73021806
|
G | T | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.796+4498G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021806 | ||||||
chr5:73021809
|
A | C | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.796+4501A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021809 | ||||||
chr5:73021883
|
A | T | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.796+4575A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021883 | ||||||
chr5:73021895
|
G | A | 24 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0152others(21): Show | 24 | HG00544.hp1 HG01258.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.796+4587G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021895 | ||||||
chr5:73022090
|
A | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.796+4782A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022090 | ||||||
chr5:73022214
|
T | C | 1 | a0002c0002t0002g0025 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.796+4906T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022214 | ||||||
chr5:73022418
|
T | G | 1 | a0002c0002t0002g0007 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.796+5110T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022418 | ||||||
chr5:73022475
|
G | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0003t0005g0107others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.796+5167G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022475 | ||||||
chr5:73022498
|
C | T | 1 | a0006c0007t0003g0268 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.796+5190C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022498 | ||||||
chr5:73022552
|
G | A | 2 | a0001c0004t0009g0282a0001c0004t0009g0283 | 2 | NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.796+5244G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022552 | ||||||
chr5:73022571
|
C | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.796+5263C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022571 | ||||||
chr5:73022721
|
A | T | 6 | a0001c0003t0004g0078a0001c0003t0004g0079a0001c0003t0004g0081others(3): Show | 6 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.796+5413A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022721 | ||||||
chr5:73023437
|
C | G | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+6129C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023437 | ||||||
chr5:73023559
|
G | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+6251G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023559 | ||||||
chr5:73023625
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0003t0005g0109 | 3 | HG02559.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.796+6317G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023625 | ||||||
chr5:73023700
|
CA | C | 29 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.796+6406delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73023700 | |||||
chr5:73023731
|
A | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+6423A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023731 | ||||||
chr5:73023789
|
G | A | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.796+6481G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023789 | ||||||
chr5:73023856
|
T | G | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+6548T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023856 | ||||||
chr5:73023919
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0138 | 3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.796+6611A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023919 | ||||||
chr5:73024095
|
T | C | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.796+6787T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024095 | ||||||
chr5:73024146
|
A | T | 1 | a0001c0003t0004g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.796+6838A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024146 | ||||||
chr5:73024185
|
A | G | 101 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0003t0003g0099others(98): Show | 101 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.796+6877A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024185 | ||||||
chr5:73024475
|
C | T | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.796+7167C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024475 | ||||||
chr5:73024478
|
C | T | 1 | a0002c0002t0002g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.796+7170C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024478 | ||||||
chr5:73024576
|
T | C | 265 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.796+7268T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024576 | ||||||
chr5:73024629
|
G | T | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.796+7321G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024629 | ||||||
chr5:73024631
|
G | A | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+7323G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024631 | ||||||
chr5:73024731
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.796+7423G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024731 | ||||||
chr5:73024784
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.796+7476A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024784 | ||||||
chr5:73024967
|
A | G | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.796+7659A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024967 | ||||||
chr5:73025265
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.796+7957A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025265 | ||||||
chr5:73025351
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG01258.hp2 HG02148.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+8043G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025351 | ||||||
chr5:73025375
|
A | AT | 38 | a0001c0001t0001g0138a0001c0001t0001g0180a0001c0001t0001g0211others(35): Show | 38 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.796+8087dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73025375 | |||||
chr5:73025375
|
AT | A | 47 | a0001c0001t0001g0130a0001c0003t0003g0278a0001c0003t0003g0279others(44): Show | 47 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.796+8087delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73025375 | |||||
chr5:73025408
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.796+8100C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025408 | ||||||
chr5:73025506
|
A | G | 1 | a0002c0002t0002g0113 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.796+8198A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025506 | ||||||
chr5:73025577
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.796+8269C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025577 | ||||||
chr5:73025628
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.796+8320C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025628 | ||||||
chr5:73025707
|
G | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.796+8399G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025707 | ||||||
chr5:73026008
|
A | AT | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.797-8648dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73026008 | |||||
chr5:73026054
|
C | T | 49 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(46): Show | 49 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.797-8603C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026054 | ||||||
chr5:73026061
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.797-8596C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026061 | ||||||
chr5:73026082
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.797-8575A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026082 | ||||||
chr5:73026116
|
A | T | 1 | a0001c0001t0001g0217 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.797-8541A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026116 | ||||||
chr5:73026119
|
G | A | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.797-8538G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026119 | ||||||
chr5:73026554
|
A | G | 1 | a0002c0002t0002g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.797-8103A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026554 | ||||||
chr5:73026631
|
C | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.797-8026C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026631 | ||||||
chr5:73026787
|
G | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.797-7870G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026787 | ||||||
chr5:73026911
|
C | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.797-7746C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026911 | ||||||
chr5:73026924
|
T | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.797-7733T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026924 | ||||||
chr5:73026939
|
G | C | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.797-7718G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026939 | ||||||
chr5:73027006
|
T | G | 2 | a0001c0001t0001g0183a0001c0004t0003g0274 | 2 | HG01069.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.797-7651T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027006 | ||||||
chr5:73027021
|
T | G | 1 | a0001c0001t0015g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.797-7636T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027021 | ||||||
chr5:73027021
|
T | TG | 4 | a0001c0001t0001g0161a0001c0001t0001g0207a0002c0002t0002g0060others(1): Show | 4 | HG02027.hp1 HG02056.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-7636_797-7635i others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027021 | ||||||
chr5:73027021
|
T | TTG | 6 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(3): Show | 6 | HG00621.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.797-7635_797-7634i others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73027021 | |||||
chr5:73027022
|
T | G | 64 | a0001c0001t0001g0117a0001c0001t0001g0139a0001c0001t0001g0152others(61): Show | 65 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.797-7635T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027022 | ||||||
chr5:73027022
|
T | TG | 90 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(87): Show | 90 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.797-7635_797-7634i others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027022 | ||||||
chr5:73027030
|
T | G | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-7627T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027030 | ||||||
chr5:73027037
|
T | A | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.797-7620T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027037 | ||||||
chr5:73027077
|
G | A | 1 | a0001c0004t0003g0239 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.797-7580G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027077 | ||||||
chr5:73027303
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0133 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.797-7354A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027303 | ||||||
chr5:73027369
|
C | CT | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.797-7275dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73027369 | |||||
chr5:73027493
|
A | G | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.797-7164A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027493 | ||||||
chr5:73027523
|
A | G | 16 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-7134A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027523 | ||||||
chr5:73027876
|
A | G | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.797-6781A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027876 | ||||||
chr5:73027881
|
A | T | 96 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.797-6776A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027881 | ||||||
chr5:73028064
|
G | A | 1 | a0002c0002t0002g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.797-6593G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73028064 | ||||||
chr5:73028646
|
C | CT | 80 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0152others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.797-5990dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028646 | |||||
chr5:73028646
|
C | CTT | 11 | a0001c0003t0004g0078a0001c0003t0004g0079a0001c0003t0004g0081others(8): Show | 11 | HG00609.hp2 HG02080.hp1 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.797-5991_797-5990d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028646 | |||||
chr5:73028646
|
CT | C | 7 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(4): Show | 7 | HG00423.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.797-5990delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028646 | |||||
chr5:73028672
|
CA | C | 96 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.797-5983delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028672 | |||||
chr5:73028816
|
A | G | 1 | a0002c0002t0002g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.797-5841A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73028816 | ||||||
chr5:73029128
|
A | C | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-5529A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029128 | ||||||
chr5:73029468
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.797-5189A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029468 | ||||||
chr5:73029507
|
T | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.797-5150T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029507 | ||||||
chr5:73029544
|
A | G | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-5113A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029544 | ||||||
chr5:73029605
|
A | C | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.797-5052A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029605 | ||||||
chr5:73029999
|
T | C | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.797-4658T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029999 | ||||||
chr5:73030000
|
CTTTTT | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.797-4654_797-4650d others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73030000 | |||||
chr5:73030044
|
T | G | 1 | a0001c0003t0004g0095 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.797-4613T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030044 | ||||||
chr5:73030045
|
G | GT | 44 | a0001c0001t0001g0151a0001c0001t0001g0168a0001c0001t0001g0170others(41): Show | 44 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.797-4598dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73030045 | |||||
chr5:73030045
|
G | GTT | 60 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(57): Show | 60 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.797-4599_797-4598d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73030045 | |||||
chr5:73030045
|
G | T | 1 | a0001c0003t0004g0095 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.797-4612G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030045 | ||||||
chr5:73030103
|
A | G | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.797-4554A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030103 | ||||||
chr5:73030143
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.797-4514G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030143 | ||||||
chr5:73030278
|
G | A | 1 | a0001c0004t0003g0273 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.797-4379G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030278 | ||||||
chr5:73030304
|
A | G | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.797-4353A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030304 | ||||||
chr5:73030543
|
G | C | 1 | a0002c0002t0002g0018 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.797-4114G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030543 | ||||||
chr5:73030617
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.797-4040G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030617 | ||||||
chr5:73030842
|
A | C | 2 | a0001c0003t0004g0081a0001c0003t0004g0095 | 2 | HG00423.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.797-3815A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030842 | ||||||
chr5:73031090
|
AC | A | 5 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-3565delC | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73031090 | |||||
chr5:73031212
|
T | C | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.797-3445T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031212 | ||||||
chr5:73031316
|
G | T | 1 | a0002c0002t0002g0013 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.797-3341G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031316 | ||||||
chr5:73031530
|
G | C | 2 | a0001c0003t0003g0277a0001c0003t0003g0278 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.797-3127G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031530 | ||||||
chr5:73031626
|
G | A | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.797-3031G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031626 | ||||||
chr5:73031674
|
A | G | 2 | a0001c0003t0006g0101a0001c0003t0006g0103 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.797-2983A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031674 | ||||||
chr5:73031808
|
G | A | 2 | a0001c0003t0006g0101a0001c0003t0006g0103 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.797-2849G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031808 | ||||||
chr5:73031994
|
T | A | 1 | a0001c0001t0007g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.797-2663T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031994 | ||||||
chr5:73032233
|
G | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA18942.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.797-2424G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032233 | ||||||
chr5:73032348
|
G | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.797-2309G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032348 | ||||||
chr5:73032880
|
AG | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0019g0158 | 3 | NA18939.hp2 NA19060.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.797-1776delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032880 | ||||||
chr5:73032965
|
C | T | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.797-1692C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032965 | ||||||
chr5:73033057
|
G | C | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.797-1600G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033057 | ||||||
chr5:73033091
|
C | A | 1 | a0002c0002t0002g0025 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.797-1566C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033091 | ||||||
chr5:73033248
|
T | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.797-1409T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033248 | ||||||
chr5:73033384
|
G | T | 2 | a0001c0004t0003g0274a0001c0004t0003g0276 | 2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.797-1273G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033384 | ||||||
chr5:73033410
|
A | T | 1 | a0002c0002t0002g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.797-1247A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033410 | ||||||
chr5:73033430
|
C | T | 16 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-1227C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033430 | ||||||
chr5:73033707
|
A | C | 2 | a0001c0003t0004g0093a0001c0003t0004g0094 | 2 | HG01261.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.797-950A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033707 | ||||||
chr5:73033885
|
T | G | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.797-772T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033885 | ||||||
chr5:73033894
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.797-763T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033894 | ||||||
chr5:73033965
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.797-692T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033965 | ||||||
chr5:73034062
|
A | G | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.797-595A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034062 | ||||||
chr5:73034163
|
C | T | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.797-494C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034163 | ||||||
chr5:73034289
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0138 | 3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.797-368C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034289 | ||||||
chr5:73034504
|
T | TTAAC | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.797-151_797-150ins others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73034504 | |||||
chr5:73034545
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.797-112G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034545 | ||||||
chr5:73034904
|
G | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.841+203G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73034904 | ||||||
chr5:73035200
|
T | G | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.841+499T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035200 | ||||||
chr5:73035302
|
C | T | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.841+601C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035302 | ||||||
chr5:73035305
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.841+604G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035305 | ||||||
chr5:73035307
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.841+606T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035307 | ||||||
chr5:73035847
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.841+1146T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035847 | ||||||
chr5:73035860
|
T | C | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.841+1159T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035860 | ||||||
chr5:73035905
|
G | A | 41 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(38): Show | 41 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.841+1204G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035905 | ||||||
chr5:73035961
|
G | A | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.842-1182G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035961 | ||||||
chr5:73035967
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0138 | 3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.842-1176C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035967 | ||||||
chr5:73035995
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.842-1148A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035995 | ||||||
chr5:73036034
|
C | T | 1 | a0002c0002t0002g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.842-1109C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036034 | ||||||
chr5:73036037
|
G | C | 1 | a0001c0003t0004g0092 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.842-1106G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036037 | ||||||
chr5:73036081
|
G | C | 4 | a0001c0003t0004g0086a0001c0003t0004g0087a0001c0003t0004g0098others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.842-1062G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036081 | ||||||
chr5:73036083
|
T | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.842-1060T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036083 | ||||||
chr5:73036139
|
C | T | 1 | a0001c0003t0008g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.842-1004C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036139 | ||||||
chr5:73036233
|
A | T | 61 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(58): Show | 62 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.842-910A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036233 | ||||||
chr5:73036478
|
A | G | 6 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-665A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036478 | ||||||
chr5:73036498
|
C | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.842-645C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036498 | ||||||
chr5:73036645
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.842-498G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036645 | ||||||
chr5:73036667
|
C | T | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.842-476C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036667 | ||||||
chr5:73036856
|
G | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.842-287G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036856 | ||||||
chr5:73037315
|
C | CAAAAGTA others(296): Show |
2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.914+114_914+115ins others(303): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037315
|
C | CAAAAGTA others(289): Show |
2 | a0001c0003t0003g0279a0004c0008t0003g0280 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.914+114_914+115ins others(296): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037315
|
C | CAAAAGTA others(290): Show |
1 | a0001c0003t0003g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.914+114_914+115ins others(297): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037315
|
C | CAAAAGTA others(295): Show |
5 | a0001c0003t0003g0277a0001c0003t0003g0278a0001c0003t0008g0111others(2): Show | 5 | HG03139.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+114_914+115ins others(302): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037315
|
C | CAAAAGTA others(296): Show |
34 | a0001c0003t0008g0110a0001c0004t0003g0237a0001c0004t0003g0238others(31): Show | 34 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.914+114_914+115ins others(303): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037315
|
C | CAAAAGTA others(297): Show |
8 | a0001c0004t0003g0243a0001c0004t0003g0256a0001c0004t0003g0264others(5): Show | 8 | HG00609.hp1 HG00735.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.914+114_914+115ins others(304): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037315
|
C | CAAAAGTA others(299): Show |
2 | a0001c0004t0003g0263a0001c0004t0003g0270 | 2 | HG02080.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.914+114_914+115ins others(306): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037315
|
C | CAAAAGTA others(296): Show |
1 | a0001c0004t0003g0244 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.914+114_914+115ins others(303): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | |||||
chr5:73037322
|
A | G | 1 | a0002c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.914+107A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037322 | ||||||
chr5:73037544
|
C | G | 45 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(42): Show | 45 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.914+329C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037544 | ||||||
chr5:73037706
|
A | G | 4 | a0001c0001t0007g0228a0001c0001t0007g0229a0001c0001t0007g0230others(1): Show | 4 | HG01081.hp2 HG01496.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.914+491A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037706 | ||||||
chr5:73037720
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+505A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037720 | ||||||
chr5:73037904
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.914+689G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037904 | ||||||
chr5:73038150
|
TTTTG | T | 4 | a0002c0002t0002g0029a0002c0002t0002g0041a0002c0002t0002g0065others(1): Show | 4 | HG02559.hp1 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+951_914+954del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73038150 | |||||
chr5:73038187
|
T | A | 6 | a0001c0004t0003g0241a0001c0004t0003g0247a0001c0004t0003g0249others(3): Show | 6 | NA18940.hp2 NA18941.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.914+972T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038187 | ||||||
chr5:73038248
|
A | G | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.914+1033A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038248 | ||||||
chr5:73038434
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.914+1219C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038434 | ||||||
chr5:73038552
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18998.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.914+1337A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038552 | ||||||
chr5:73038733
|
A | G | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+1518A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038733 | ||||||
chr5:73038758
|
C | T | 1 | a0001c0004t0003g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.914+1543C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038758 | ||||||
chr5:73038765
|
C | T | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.914+1550C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038765 | ||||||
chr5:73039036
|
A | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.914+1821A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039036 | ||||||
chr5:73039320
|
A | T | 2 | a0001c0004t0003g0244a0001c0004t0003g0250 | 2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.915-1971A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039320 | ||||||
chr5:73039326
|
A | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.915-1965A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039326 | ||||||
chr5:73039348
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.915-1943A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039348 | ||||||
chr5:73039452
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.915-1839A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039452 | ||||||
chr5:73039500
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.915-1791A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039500 | ||||||
chr5:73039660
|
G | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0142others(1): Show | 4 | NA18942.hp1 NA18990.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-1631G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039660 | ||||||
chr5:73039681
|
AT | A | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.915-1606delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73039681 | |||||
chr5:73039812
|
C | T | 7 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.915-1479C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039812 | ||||||
chr5:73039864
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.915-1427G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039864 | ||||||
chr5:73039876
|
C | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.915-1415C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039876 | ||||||
chr5:73039881
|
C | T | 170 | a0001c0001t0001g0206a0001c0003t0003g0099a0001c0003t0003g0100others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.915-1410C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039881 | ||||||
chr5:73039918
|
TA | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-1371delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73039918 | |||||
chr5:73039931
|
C | T | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.915-1360C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039931 | ||||||
chr5:73039954
|
AAAG | A | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-1328_915-1326d others(5): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73039954 | |||||
chr5:73040012
|
G | A | 1 | a0001c0003t0006g0102 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.915-1279G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040012 | ||||||
chr5:73040203
|
A | T | 3 | a0001c0004t0003g0242a0001c0004t0003g0284a0001c0004t0003g0285 | 3 | NA18982.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.915-1088A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040203 | ||||||
chr5:73040591
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0184 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.915-700A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040591 | ||||||
chr5:73040792
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.915-499G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040792 | ||||||
chr5:73040998
|
A | T | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.915-293A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040998 | ||||||
chr5:73041043
|
T | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.915-248T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73041043 | ||||||
chr5:73041165
|
T | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.915-126T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73041165 | ||||||
chr5:73041202
|
A | G | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.915-89A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73041202 | ||||||
chr5:73041517
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.939+202A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041517 | ||||||
chr5:73041621
|
T | C | 3 | a0001c0004t0003g0262a0001c0004t0003g0266a0001c0004t0012g0265 | 3 | HG00558.hp2 HG02056.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.939+306T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041621 | ||||||
chr5:73041736
|
C | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+421C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041736 | ||||||
chr5:73041910
|
A | G | 6 | a0001c0004t0003g0241a0001c0004t0003g0247a0001c0004t0003g0249others(3): Show | 6 | NA18940.hp2 NA18941.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+595A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041910 | ||||||
chr5:73041919
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.939+604A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041919 | ||||||
chr5:73041937
|
G | A | 1 | a0001c0004t0003g0266 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.939+622G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041937 | ||||||
chr5:73041986
|
A | G | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.939+671A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041986 | ||||||
chr5:73042024
|
C | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.939+709C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042024 | ||||||
chr5:73042142
|
G | A | 1 | a0001c0004t0012g0265 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.939+827G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042142 | ||||||
chr5:73042143
|
G | A | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.939+828G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042143 | ||||||
chr5:73042216
|
G | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.939+901G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042216 | ||||||
chr5:73042284
|
C | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.939+969C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042284 | ||||||
chr5:73042348
|
A | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.939+1033A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042348 | ||||||
chr5:73042642
|
T | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.939+1327T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042642 | ||||||
chr5:73042900
|
C | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.939+1585C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042900 | ||||||
chr5:73042945
|
T | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.939+1630T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042945 | ||||||
chr5:73043106
|
CTTTTTTT others(5): Show |
C | 21 | a0001c0001t0001g0117a0001c0001t0001g0152a0001c0001t0001g0154others(18): Show | 21 | HG00544.hp1 HG01258.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.939+1793_939+1804d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73043106 | |||||
chr5:73043154
|
C | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.939+1839C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043154 | ||||||
chr5:73043282
|
T | C | 169 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.939+1967T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043282 | ||||||
chr5:73043283
|
G | A | 1 | a0001c0004t0003g0262 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.939+1968G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043283 | ||||||
chr5:73043336
|
A | G | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.939+2021A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043336 | ||||||
chr5:73043406
|
A | T | 1 | a0001c0003t0004g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.939+2091A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043406 | ||||||
chr5:73043409
|
TAC | T | 97 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.939+2110_939+2111d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73043409 | |||||
chr5:73043540
|
AATAG | A | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+2229_939+2232d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73043540 | |||||
chr5:73043725
|
G | A | 1 | a0004c0008t0003g0280 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.939+2410G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043725 | ||||||
chr5:73043749
|
G | A | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.939+2434G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043749 | ||||||
chr5:73043922
|
G | T | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.939+2607G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043922 | ||||||
chr5:73044251
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+2936C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044251 | ||||||
chr5:73044339
|
G | A | 1 | a0001c0004t0003g0264 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.939+3024G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044339 | ||||||
chr5:73044384
|
A | G | 1 | a0001c0003t0004g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+3069A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044384 | ||||||
chr5:73044430
|
A | G | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.939+3115A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044430 | ||||||
chr5:73044598
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+3283A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044598 | ||||||
chr5:73044854
|
G | A | 1 | a0002c0002t0002g0233 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.939+3539G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044854 | ||||||
chr5:73044957
|
A | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+3642A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044957 | ||||||
chr5:73045519
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.939+4204T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73045519 | ||||||
chr5:73045527
|
A | C | 1 | a0002c0002t0002g0004 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+4212A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73045527 | ||||||
chr5:73045691
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.939+4376A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73045691 | ||||||
chr5:73046089
|
G | C | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.939+4774G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046089 | ||||||
chr5:73046295
|
G | A | 1 | a0002c0002t0002g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.939+4980G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046295 | ||||||
chr5:73046393
|
G | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.940-4956G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046393 | ||||||
chr5:73046864
|
A | G | 16 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.940-4485A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046864 | ||||||
chr5:73046889
|
T | A | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.940-4460T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046889 | ||||||
chr5:73046972
|
G | C | 1 | a0001c0003t0004g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.940-4377G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046972 | ||||||
chr5:73047038
|
C | A | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.940-4311C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047038 | ||||||
chr5:73047157
|
CTGTT | C | 3 | a0001c0001t0001g0130a0001c0003t0005g0002a0003c0006t0005g0003 | 3 | HG02451.hp1 HG02723.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.940-4188_940-4185d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73047157 | |||||
chr5:73047159
|
G | C | 3 | a0002c0002t0002g0033a0002c0002t0002g0037a0002c0002t0002g0059 | 3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.940-4190G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047159 | ||||||
chr5:73047168
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-4181T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047168 | ||||||
chr5:73047209
|
C | T | 2 | a0001c0003t0003g0277a0001c0003t0003g0278 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.940-4140C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047209 | ||||||
chr5:73047400
|
T | G | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0204 | 3 | NA18971.hp2 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.940-3949T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047400 | ||||||
chr5:73047422
|
A | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940-3927A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047422 | ||||||
chr5:73047562
|
C | CT | 7 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0019g0158others(4): Show | 7 | HG02257.hp1 HG03098.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.940-3773dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73047562 | |||||
chr5:73047562
|
CT | C | 31 | a0001c0001t0001g0135a0001c0003t0004g0071a0001c0003t0004g0072others(28): Show | 31 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-3773delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73047562 | |||||
chr5:73047627
|
A | G | 1 | a0005c0011t0004g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.940-3722A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047627 | ||||||
chr5:73048029
|
A | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.940-3320A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048029 | ||||||
chr5:73048050
|
C | A | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.940-3299C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048050 | ||||||
chr5:73048051
|
T | G | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.940-3298T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048051 | ||||||
chr5:73048088
|
GC | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.940-3258delC | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048088 | |||||
chr5:73048108
|
C | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940-3241C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048108 | ||||||
chr5:73048215
|
C | T | 1 | a0001c0004t0003g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.940-3134C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048215 | ||||||
chr5:73048239
|
C | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.940-3110C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048239 | ||||||
chr5:73048243
|
A | G | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.940-3106A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048243 | ||||||
chr5:73048335
|
A | C | 2 | a0002c0002t0002g0049a0002c0002t0002g0187 | 2 | NA18947.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.940-3014A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048335 | ||||||
chr5:73048479
|
A | G | 1 | a0002c0002t0002g0013 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.940-2870A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048479 | ||||||
chr5:73048585
|
G | A | 1 | a0001c0004t0009g0283 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.940-2764G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048585 | ||||||
chr5:73048781
|
TTA | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.940-2566_940-2565d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048781 | |||||
chr5:73048833
|
C | CTA | 4 | a0001c0001t0001g0152a0001c0001t0001g0202a0001c0001t0001g0208others(1): Show | 4 | HG00544.hp1 NA18973.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-2515_940-2514d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048833 | |||||
chr5:73048843
|
A | C | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-2506A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048843 | ||||||
chr5:73048870
|
C | CT | 26 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(23): Show | 26 | HG00423.hp1 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.940-2455dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048870 | |||||
chr5:73048870
|
CT | C | 12 | a0001c0001t0001g0188a0001c0003t0004g0081a0001c0003t0005g0105others(9): Show | 12 | HG00609.hp2 HG01169.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.940-2455delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048870 | |||||
chr5:73048969
|
C | T | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.940-2380C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048969 | ||||||
chr5:73049095
|
C | T | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.940-2254C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049095 | ||||||
chr5:73049127
|
C | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.940-2222C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049127 | ||||||
chr5:73049444
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940-1905C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049444 | ||||||
chr5:73049540
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.940-1809C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049540 | ||||||
chr5:73049682
|
T | A | 90 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(87): Show | 90 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.940-1667T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049682 | ||||||
chr5:73049703
|
C | G | 1 | a0001c0003t0003g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.940-1646C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049703 | ||||||
chr5:73049765
|
T | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.940-1584T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049765 | ||||||
chr5:73049936
|
T | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.940-1413T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049936 | ||||||
chr5:73050144
|
A | G | 1 | a0002c0002t0002g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.940-1205A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050144 | ||||||
chr5:73050187
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-1162C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050187 | ||||||
chr5:73050293
|
G | GCTAT | 23 | a0001c0003t0003g0279a0001c0003t0003g0281a0001c0004t0003g0242others(20): Show | 23 | HG00735.hp1 HG01081.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.940-1055_940-1052d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050293 | |||||
chr5:73050294
|
C | CTATCTAT others(1): Show |
18 | a0001c0004t0003g0241a0001c0004t0003g0247a0001c0004t0003g0252others(15): Show | 18 | HG00558.hp2 HG00609.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.940-1052_940-1051i others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
C | CTATCTAT others(5): Show |
3 | a0001c0003t0003g0100a0001c0003t0003g0277a0001c0004t0003g0249 | 3 | HG02965.hp2 HG03225.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.940-1052_940-1051i others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
C | CTATCTAT others(9): Show |
2 | a0001c0003t0003g0099a0001c0003t0003g0278 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.940-1052_940-1051i others(18): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
C | CTATT | 31 | a0001c0001t0001g0119a0001c0001t0001g0174a0001c0001t0001g0178others(28): Show | 31 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.940-1013_940-1010d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
C | CTATTTAT others(1): Show |
20 | a0001c0001t0001g0141a0001c0001t0001g0151a0001c0001t0001g0168others(17): Show | 20 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.940-1017_940-1010d others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
C | CTATTTAT others(5): Show |
1 | a0001c0003t0004g0083 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.940-1021_940-1010d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
CTATT | C | 8 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-1013_940-1010d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
CTATTTAT others(1): Show |
C | 7 | a0001c0003t0005g0002a0001c0003t0005g0105a0001c0003t0005g0106others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-1017_940-1010d others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
CTATTTAT others(5): Show |
C | 15 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0155others(12): Show | 15 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.940-1021_940-1010d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050294
|
CTATTTAT others(9): Show |
C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.940-1025_940-1010d others(18): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | |||||
chr5:73050298
|
T | C | 6 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0004t0003g0239others(3): Show | 6 | HG00621.hp2 HG02071.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-1051T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050298 | ||||||
chr5:73050302
|
T | C | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.940-1047T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050302 | ||||||
chr5:73050411
|
TG | T | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-935delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050411 | |||||
chr5:73050564
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0184a0001c0001t0001g0188 | 3 | HG03041.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.940-785G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050564 | ||||||
chr5:73051263
|
A | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.940-86A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73051263 | ||||||
chr5:73051289
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.940-60A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73051289 | ||||||
chr5:73051516
|
A | C | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+110A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051516 | ||||||
chr5:73051586
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.997+180A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051586 | ||||||
chr5:73051700
|
T | G | 169 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.997+294T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051700 | ||||||
chr5:73051814
|
C | T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.997+408C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051814 | ||||||
chr5:73052084
|
G | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.998-248G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73052084 | ||||||
chr5:73052106
|
G | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998-226G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73052106 | ||||||
chr5:73052203
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.998-129G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73052203 | ||||||
chr5:73052619
|
C | T | 1 | a0001c0003t0004g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1173+112C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73052619 | ||||||
chr5:73052725
|
G | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1173+218G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73052725 | ||||||
chr5:73053038
|
C | T | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+531C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053038 | ||||||
chr5:73053039
|
C | A | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+532C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053039 | ||||||
chr5:73053040
|
A | T | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+533A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053040 | ||||||
chr5:73053041
|
G | A | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+534G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053041 | ||||||
chr5:73053042
|
T | C | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+535T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053042 | ||||||
chr5:73053044
|
A | T | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+537A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053044 | ||||||
chr5:73053046
|
T | G | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+539T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053046 | ||||||
chr5:73053048
|
T | G | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+541T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053048 | ||||||
chr5:73053049
|
T | A | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+542T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053049 | ||||||
chr5:73053051
|
T | G | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+544T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053051 | ||||||
chr5:73053052
|
C | T | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+545C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053052 | ||||||
chr5:73053053
|
C | T | 1 | a0001c0004t0003g0255 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+546C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053053 | ||||||
chr5:73053183
|
T | A | 2 | a0002c0002t0002g0011a0002c0002t0002g0012 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1173+676T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053183 | ||||||
chr5:73053260
|
T | C | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1173+753T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053260 | ||||||
chr5:73053275
|
C | A | 5 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+768C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053275 | ||||||
chr5:73053305
|
TTTTCTTC others(12): Show |
T | 1 | a0002c0002t0002g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1173+804_1173+822d others(21): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053305 | |||||
chr5:73053363
|
C | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1174-797C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053363 | ||||||
chr5:73053437
|
T | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1174-723T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053437 | ||||||
chr5:73053444
|
C | G | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1174-716C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053444 | ||||||
chr5:73053650
|
T | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1174-510T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053650 | ||||||
chr5:73053653
|
A | G | 2 | a0001c0003t0003g0277a0001c0003t0003g0278 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1174-507A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053653 | ||||||
chr5:73053657
|
C | G | 2 | a0001c0004t0003g0244a0001c0004t0003g0250 | 2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1174-503C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053657 | ||||||
chr5:73053695
|
CA | C | 96 | a0001c0001t0001g0129a0001c0003t0003g0099a0001c0003t0003g0100others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1174-449delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053695 | |||||
chr5:73053757
|
G | A | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1174-403G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053757 | ||||||
chr5:73053886
|
C | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1174-274C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053886 | ||||||
chr5:73053897
|
TAA | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1174-258_1174-257d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053897 | |||||
chr5:73053915
|
TATTA | T | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-241_1174-238d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053915 | |||||
chr5:73054323
|
G | A | 5 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185+152G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 14/25 | chr5 | 73054323 | ||||||
chr5:73054340
|
A | T | 1 | a0002c0002t0002g0115 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1185+169A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 14/25 | chr5 | 73054340 | ||||||
chr5:73054463
|
A | T | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1186-62A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 14/25 | chr5 | 73054463 | ||||||
chr5:73054705
|
G | A | 8 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1210+156G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054705 | ||||||
chr5:73054763
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1210+214A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054763 | ||||||
chr5:73054961
|
T | C | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210+412T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054961 | ||||||
chr5:73054969
|
G | T | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210+420G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054969 | ||||||
chr5:73055040
|
A | G | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1210+491A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055040 | ||||||
chr5:73055235
|
C | G | 169 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1210+686C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055235 | ||||||
chr5:73055353
|
T | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1211-712T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055353 | ||||||
chr5:73055577
|
C | T | 2 | a0002c0002t0002g0044a0002c0002t0002g0056 | 2 | NA18612.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1211-488C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055577 | ||||||
chr5:73055670
|
A | G | 1 | a0001c0003t0004g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1211-395A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055670 | ||||||
chr5:73055695
|
C | T | 1 | a0001c0003t0004g0082 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1211-370C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055695 | ||||||
chr5:73055706
|
C | T | 3 | a0001c0003t0005g0107a0001c0003t0005g0108a0001c0003t0005g0109 | 3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1211-359C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055706 | ||||||
chr5:73055806
|
G | A | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1211-259G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055806 | ||||||
chr5:73055881
|
T | A | 169 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1211-184T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055881 | ||||||
chr5:73055996
|
T | G | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1211-69T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055996 | ||||||
chr5:73056255
|
C | A | 1 | a0001c0003t0003g0277 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1253+148C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056255 | ||||||
chr5:73056447
|
C | G | 1 | a0001c0003t0005g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1253+340C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056447 | ||||||
chr5:73056461
|
A | G | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1253+354A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056461 | ||||||
chr5:73056487
|
T | C | 283 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.1253+380T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056487 | ||||||
chr5:73056884
|
T | C | 1 | a0002c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1253+777T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056884 | ||||||
chr5:73056941
|
C | T | 60 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(57): Show | 60 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1253+834C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056941 | ||||||
chr5:73056945
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02040.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1253+838C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056945 | ||||||
chr5:73057047
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1253+940C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057047 | ||||||
chr5:73057071
|
C | T | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1253+964C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057071 | ||||||
chr5:73057102
|
A | AT | 168 | a0001c0001t0001g0117a0001c0003t0003g0099a0001c0003t0003g0100others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1253+1007dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr5 | 73057102 | |||||
chr5:73057103
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1253+996T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057103 | ||||||
chr5:73057220
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1253+1113C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057220 | ||||||
chr5:73057321
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0133 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1254-1112G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057321 | ||||||
chr5:73057379
|
T | A | 2 | a0001c0003t0003g0277a0001c0003t0003g0278 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1254-1054T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057379 | ||||||
chr5:73057481
|
T | C | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1254-952T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057481 | ||||||
chr5:73057599
|
G | A | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1254-834G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057599 | ||||||
chr5:73058002
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1254-431T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73058002 | ||||||
chr5:73058399
|
G | A | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1254-34G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73058399 | ||||||
chr5:73058613
|
T | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1345+89T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058613 | ||||||
chr5:73058730
|
G | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+206G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058730 | ||||||
chr5:73058776
|
C | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1345+252C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058776 | ||||||
chr5:73058939
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1345+415G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058939 | ||||||
chr5:73059031
|
A | C | 2 | a0001c0003t0006g0101a0001c0003t0006g0103 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1345+507A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059031 | ||||||
chr5:73059060
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1345+536T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059060 | ||||||
chr5:73059070
|
T | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1345+546T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059070 | ||||||
chr5:73059107
|
TCAAAAAG others(7): Show |
T | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1345+590_1345+603d others(16): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73059107 | |||||
chr5:73059247
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1345+723C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059247 | ||||||
chr5:73059570
|
ATTGGTTT | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1345+1049_1345+105 others(11): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73059570 | |||||
chr5:73059622
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0198 | 2 | NA18947.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1345+1098A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059622 | ||||||
chr5:73059768
|
T | A | 1 | a0002c0002t0002g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1345+1244T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059768 | ||||||
chr5:73060162
|
A | G | 1 | a0001c0003t0003g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1345+1638A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060162 | ||||||
chr5:73060325
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1345+1801A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060325 | ||||||
chr5:73060354
|
A | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1345+1830A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060354 | ||||||
chr5:73060424
|
A | G | 1 | a0001c0003t0004g0095 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1345+1900A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060424 | ||||||
chr5:73060768
|
GTGT | G | 8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345+2249_1345+225 others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73060768 | |||||
chr5:73060963
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0138 | 3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1345+2439A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060963 | ||||||
chr5:73061007
|
C | CA | 71 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0130others(68): Show | 71 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1345+2497dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73061007 | |||||
chr5:73061007
|
C | CAA | 11 | a0001c0003t0003g0281a0001c0003t0005g0002a0001c0003t0005g0107others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1345+2496_1345+249 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73061007 | |||||
chr5:73061007
|
C | CAAA | 25 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.1345+2495_1345+249 others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73061007 | |||||
chr5:73061078
|
C | A | 278 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.1345+2554C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061078 | ||||||
chr5:73061124
|
C | G | 1 | a0001c0001t0007g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1345+2600C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061124 | ||||||
chr5:73061259
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1346-2582G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061259 | ||||||
chr5:73061493
|
C | T | 4 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0047others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-2348C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061493 | ||||||
chr5:73061612
|
A | G | 7 | a0001c0001t0001g0142a0001c0003t0005g0002a0001c0003t0006g0101others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-2229A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061612 | ||||||
chr5:73061690
|
A | G | 1 | a0001c0003t0003g0277 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1346-2151A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061690 | ||||||
chr5:73061821
|
G | A | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1346-2020G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061821 | ||||||
chr5:73061866
|
G | C | 1 | a0001c0001t0018g0226 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1346-1975G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061866 | ||||||
chr5:73061868
|
T | A | 1 | a0001c0001t0007g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1346-1973T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061868 | ||||||
chr5:73061914
|
T | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1346-1927T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061914 | ||||||
chr5:73062027
|
G | A | 1 | a0001c0003t0004g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1346-1814G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062027 | ||||||
chr5:73062051
|
C | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0166others(1): Show | 4 | NA18939.hp2 NA18957.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-1790C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062051 | ||||||
chr5:73062056
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1346-1785A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062056 | ||||||
chr5:73062303
|
A | G | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-1538A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062303 | ||||||
chr5:73062427
|
G | A | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1346-1414G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062427 | ||||||
chr5:73062962
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1346-879A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062962 | ||||||
chr5:73063008
|
T | A | 2 | a0001c0004t0009g0282a0001c0004t0009g0283 | 2 | NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1346-833T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063008 | ||||||
chr5:73063254
|
T | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0184a0001c0001t0001g0188 | 3 | HG03041.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1346-587T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063254 | ||||||
chr5:73063369
|
A | AT | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1346-471dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73063369 | |||||
chr5:73063596
|
G | C | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-245G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063596 | ||||||
chr5:73063604
|
T | C | 3 | a0001c0004t0003g0259a0001c0004t0003g0260a0006c0007t0003g0268 | 3 | NA18954.hp2 NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1346-237T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063604 | ||||||
chr5:73064011
|
A | G | 6 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+67A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064011 | ||||||
chr5:73064251
|
C | T | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1449+307C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064251 | ||||||
chr5:73064282
|
C | G | 55 | a0001c0003t0003g0277a0001c0003t0003g0278a0001c0003t0003g0279others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1449+338C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064282 | ||||||
chr5:73064538
|
A | T | 3 | a0002c0002t0002g0033a0002c0002t0002g0037a0002c0002t0002g0059 | 3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1449+594A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064538 | ||||||
chr5:73064675
|
C | T | 1 | a0001c0004t0009g0282 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1449+731C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064675 | ||||||
chr5:73064706
|
C | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1449+762C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064706 | ||||||
chr5:73064848
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1449+904A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064848 | ||||||
chr5:73064945
|
G | C | 1 | a0001c0001t0018g0226 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1449+1001G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064945 | ||||||
chr5:73064974
|
T | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1449+1030T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064974 | ||||||
chr5:73065095
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1449+1151G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065095 | ||||||
chr5:73065168
|
G | A | 1 | a0002c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1449+1224G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065168 | ||||||
chr5:73065257
|
T | C | 1 | a0001c0004t0003g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1449+1313T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065257 | ||||||
chr5:73065290
|
A | AT | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1449+1355dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73065290 | |||||
chr5:73065510
|
A | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1449+1566A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065510 | ||||||
chr5:73065624
|
T | A | 1 | a0002c0002t0002g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1449+1680T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065624 | ||||||
chr5:73065805
|
C | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1449+1861C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065805 | ||||||
chr5:73065857
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1449+1913C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065857 | ||||||
chr5:73066286
|
A | AT | 4 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0010g0009others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+2345dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73066286 | |||||
chr5:73066323
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1450-2327A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066323 | ||||||
chr5:73066462
|
A | G | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1450-2188A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066462 | ||||||
chr5:73066528
|
A | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0211 | 3 | HG00642.hp2 HG04184.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1450-2122A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066528 | ||||||
chr5:73066575
|
C | CT | 35 | a0001c0003t0003g0281a0001c0003t0004g0071a0001c0003t0004g0072others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1450-2056dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73066575 | |||||
chr5:73066575
|
CT | C | 118 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(115): Show | 118 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1450-2056delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73066575 | |||||
chr5:73066579
|
T | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1450-2071T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066579 | ||||||
chr5:73066739
|
G | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1450-1911G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066739 | ||||||
chr5:73066760
|
A | T | 1 | a0002c0002t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1450-1890A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066760 | ||||||
chr5:73067102
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1450-1548G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067102 | ||||||
chr5:73067104
|
A | C | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1450-1546A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067104 | ||||||
chr5:73067107
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0133 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1450-1543A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067107 | ||||||
chr5:73067170
|
C | A | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1450-1480C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067170 | ||||||
chr5:73067235
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1450-1415G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067235 | ||||||
chr5:73067387
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0211 | 3 | HG00642.hp2 HG04184.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1450-1263G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067387 | ||||||
chr5:73067576
|
A | G | 1 | a0001c0004t0003g0243 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1450-1074A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067576 | ||||||
chr5:73067978
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1450-672G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067978 | ||||||
chr5:73068000
|
A | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1450-650A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73068000 | ||||||
chr5:73068227
|
T | G | 2 | a0002c0002t0002g0050a0002c0002t0002g0051 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1450-423T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73068227 | ||||||
chr5:73068786
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | splice_region_variant&intron_variant | LOW | c.1579+7G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068786 | ||||||
chr5:73068831
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1579+52A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068831 | ||||||
chr5:73068834
|
C | G | 1 | a0002c0002t0002g0032 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1579+55C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068834 | ||||||
chr5:73068846
|
A | G | 115 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(112): Show | 115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1579+67A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068846 | ||||||
chr5:73068860
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1579+81G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068860 | ||||||
chr5:73068980
|
A | C | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579+201A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068980 | ||||||
chr5:73069037
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1579+258A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069037 | ||||||
chr5:73069090
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1579+311G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069090 | ||||||
chr5:73069469
|
T | A | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1579+690T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069469 | ||||||
chr5:73069504
|
G | A | 1 | a0001c0004t0003g0239 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1579+725G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069504 | ||||||
chr5:73069505
|
C | T | 115 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(112): Show | 115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1579+726C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069505 | ||||||
chr5:73069571
|
G | A | 1 | a0001c0003t0006g0102 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+792G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069571 | ||||||
chr5:73069573
|
T | C | 1 | a0001c0004t0003g0264 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1579+794T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069573 | ||||||
chr5:73069628
|
G | A | 4 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0047others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1579+849G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069628 | ||||||
chr5:73069630
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1579+851G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069630 | ||||||
chr5:73069673
|
CCTT | C | 60 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(57): Show | 60 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1579+897_1579+899d others(5): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 73069673 | |||||
chr5:73069724
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1579+945A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069724 | ||||||
chr5:73069734
|
A | G | 1 | a0001c0003t0004g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1579+955A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069734 | ||||||
chr5:73070023
|
A | G | 1 | a0002c0002t0002g0049 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1579+1244A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070023 | ||||||
chr5:73070029
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1579+1250A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070029 | ||||||
chr5:73070373
|
C | T | 1 | a0001c0004t0003g0266 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1579+1594C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070373 | ||||||
chr5:73070398
|
A | AT | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1579+1620dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 73070398 | |||||
chr5:73070565
|
GT | G | 18 | a0001c0001t0001g0132a0001c0003t0003g0099a0001c0003t0003g0100others(15): Show | 18 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1579+1802delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 73070565 | |||||
chr5:73070572
|
T | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+1793T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070572 | ||||||
chr5:73070597
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1579+1818T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070597 | ||||||
chr5:73070763
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1579+1984T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070763 | ||||||
chr5:73071044
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+2265A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071044 | ||||||
chr5:73071144
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+2365A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071144 | ||||||
chr5:73071308
|
A | T | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1579+2529A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071308 | ||||||
chr5:73071339
|
C | T | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1579+2560C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071339 | ||||||
chr5:73071345
|
T | C | 1 | a0001c0003t0005g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1579+2566T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071345 | ||||||
chr5:73071425
|
T | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1579+2646T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071425 | ||||||
chr5:73071512
|
A | G | 214 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(211): Show | 214 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.1579+2733A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071512 | ||||||
chr5:73071729
|
C | T | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+2950C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071729 | ||||||
chr5:73071790
|
G | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1580-2952G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071790 | ||||||
chr5:73071892
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1580-2850G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071892 | ||||||
chr5:73071892
|
G | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1580-2850G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071892 | ||||||
chr5:73071911
|
G | C | 1 | a0002c0002t0002g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1580-2831G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071911 | ||||||
chr5:73071918
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1580-2824G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071918 | ||||||
chr5:73071926
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-2816T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071926 | ||||||
chr5:73071974
|
A | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1580-2768A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071974 | ||||||
chr5:73072226
|
A | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1580-2516A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072226 | ||||||
chr5:73072264
|
G | A | 2 | a0001c0004t0003g0243a0001c0004t0003g0246 | 2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1580-2478G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072264 | ||||||
chr5:73072468
|
A | C | 2 | a0001c0004t0003g0263a0001c0004t0003g0270 | 2 | HG02080.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1580-2274A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072468 | ||||||
chr5:73072554
|
A | C | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1580-2188A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072554 | ||||||
chr5:73072812
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1580-1930G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072812 | ||||||
chr5:73073118
|
T | G | 2 | a0001c0003t0004g0093a0001c0003t0004g0094 | 2 | HG01261.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1580-1624T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073118 | ||||||
chr5:73073139
|
T | G | 48 | a0001c0003t0003g0279a0001c0003t0003g0281a0001c0004t0003g0237others(45): Show | 48 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1580-1603T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073139 | ||||||
chr5:73073526
|
G | A | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1580-1216G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073526 | ||||||
chr5:73073650
|
A | G | 1 | a0001c0003t0004g0081 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1580-1092A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073650 | ||||||
chr5:73073705
|
T | A | 94 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1580-1037T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073705 | ||||||
chr5:73073755
|
G | A | 1 | a0002c0002t0002g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1580-987G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073755 | ||||||
chr5:73073972
|
C | T | 4 | a0001c0003t0006g0101a0001c0003t0006g0102a0001c0003t0006g0103others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-770C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073972 | ||||||
chr5:73073974
|
C | T | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-768C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073974 | ||||||
chr5:73073994
|
G | A | 1 | a0002c0002t0002g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1580-748G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073994 | ||||||
chr5:73074038
|
C | G | 13 | a0001c0003t0004g0078a0001c0003t0004g0079a0001c0003t0004g0080others(10): Show | 13 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.1580-704C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074038 | ||||||
chr5:73074043
|
C | T | 82 | a0001c0003t0003g0277a0001c0003t0003g0278a0001c0003t0003g0279others(79): Show | 82 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1580-699C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074043 | ||||||
chr5:73074166
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1580-576G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074166 | ||||||
chr5:73074222
|
T | C | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1580-520T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074222 | ||||||
chr5:73074258
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1580-484A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074258 | ||||||
chr5:73074578
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1580-164A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074578 | ||||||
chr5:73074702
|
C | A | 15 | a0001c0001t0001g0151a0001c0001t0001g0168a0001c0001t0001g0169others(12): Show | 15 | HG00735.hp2 HG01192.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-40C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074702 | ||||||
chr5:73074918
|
C | T | 55 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1691+65C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73074918 | ||||||
chr5:73075072
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1691+219A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075072 | ||||||
chr5:73075146
|
G | C | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1691+293G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075146 | ||||||
chr5:73075318
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0133 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1691+465G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075318 | ||||||
chr5:73075542
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1691+689T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075542 | ||||||
chr5:73075704
|
C | T | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1691+851C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075704 | ||||||
chr5:73075745
|
A | G | 1 | a0002c0002t0002g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1691+892A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075745 | ||||||
chr5:73075844
|
A | G | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1691+991A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075844 | ||||||
chr5:73075900
|
A | AG | 94 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1691+1051dupG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 73075900 | |||||
chr5:73076046
|
T | A | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1691+1193T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076046 | ||||||
chr5:73076053
|
G | C | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1691+1200G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076053 | ||||||
chr5:73076058
|
A | G | 2 | a0002c0002t0002g0001a0002c0002t0002g0022 | 3 | HG01070.hp2 HG01071.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1691+1205A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076058 | ||||||
chr5:73076154
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1692-1184C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076154 | ||||||
chr5:73076157
|
G | T | 52 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(49): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1692-1181G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076157 | ||||||
chr5:73076179
|
G | C | 1 | a0001c0005t0003g0248 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1692-1159G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076179 | ||||||
chr5:73076313
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1692-1025A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076313 | ||||||
chr5:73076329
|
A | G | 1 | a0001c0003t0006g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1692-1009A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076329 | ||||||
chr5:73076333
|
C | A | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1692-1005C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076333 | ||||||
chr5:73076502
|
T | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1692-836T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076502 | ||||||
chr5:73077034
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1692-304A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077034 | ||||||
chr5:73077124
|
A | G | 1 | a0001c0003t0006g0102 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1692-214A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077124 | ||||||
chr5:73077144
|
A | G | 2 | a0001c0004t0003g0244a0001c0004t0003g0250 | 2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1692-194A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077144 | ||||||
chr5:73077208
|
G | C | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1692-130G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077208 | ||||||
chr5:73077260
|
G | A | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692-78G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077260 | ||||||
chr5:73077529
|
G | A | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1847+36G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077529 | ||||||
chr5:73077681
|
A | G | 4 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0047others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1847+188A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077681 | ||||||
chr5:73077683
|
A | AAAAAAC | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1847+193_1847+198d others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 73077683 | |||||
chr5:73077687
|
A | G | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1847+194A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077687 | ||||||
chr5:73077885
|
A | C | 100 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(97): Show | 100 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1848-295A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077885 | ||||||
chr5:73078324
|
G | A | 1 | a0002c0002t0002g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1980+12G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078324 | ||||||
chr5:73078463
|
G | A | 1 | a0002c0002t0002g0019 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1980+151G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078463 | ||||||
chr5:73078612
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | NA18612.hp2 NA18947.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1980+300A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078612 | ||||||
chr5:73078648
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1980+336A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078648 | ||||||
chr5:73078859
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1980+547C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078859 | ||||||
chr5:73078927
|
A | C | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1980+615A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078927 | ||||||
chr5:73079052
|
A | G | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1980+740A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079052 | ||||||
chr5:73079062
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0157 | 2 | HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1980+750C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079062 | ||||||
chr5:73079141
|
T | A | 1 | a0001c0003t0004g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1980+829T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079141 | ||||||
chr5:73079458
|
T | C | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1980+1146T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079458 | ||||||
chr5:73079953
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1980+1641A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079953 | ||||||
chr5:73080245
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1981-1538G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080245 | ||||||
chr5:73080306
|
T | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0142others(1): Show | 4 | NA18942.hp1 NA18990.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-1477T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080306 | ||||||
chr5:73080669
|
T | TTA | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1981-1113_1981-111 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 73080669 | |||||
chr5:73080806
|
G | A | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1981-977G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080806 | ||||||
chr5:73080881
|
C | T | 8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1981-902C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080881 | ||||||
chr5:73080889
|
T | C | 1 | a0001c0003t0005g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1981-894T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080889 | ||||||
chr5:73080913
|
C | T | 2 | a0001c0003t0005g0002a0003c0006t0005g0003 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1981-870C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080913 | ||||||
chr5:73080963
|
C | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1981-820C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080963 | ||||||
chr5:73081021
|
G | T | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1981-762G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081021 | ||||||
chr5:73081031
|
G | C | 1 | a0002c0002t0002g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1981-752G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081031 | ||||||
chr5:73081335
|
C | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1981-448C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081335 | ||||||
chr5:73081461
|
C | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1981-322C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081461 | ||||||
chr5:73081594
|
A | G | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1981-189A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081594 | ||||||
chr5:73081775
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.1981-8C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081775 | ||||||
chr5:73082050
|
A | G | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2180+68A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082050 | ||||||
chr5:73082188
|
A | C | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2180+206A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082188 | ||||||
chr5:73082260
|
C | CT | 202 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(199): Show | 202 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.2180+293dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr5 | 73082260 | |||||
chr5:73082260
|
CT | C | 6 | a0001c0003t0010g0009a0001c0003t0010g0010a0002c0002t0002g0029others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2180+293delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr5 | 73082260 | |||||
chr5:73082276
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0133 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2180+294C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082276 | ||||||
chr5:73082292
|
A | T | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2180+310A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082292 | ||||||
chr5:73082293
|
T | A | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2180+311T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082293 | ||||||
chr5:73082294
|
A | T | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2180+312A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082294 | ||||||
chr5:73082433
|
C | T | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2181-328C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082433 | ||||||
chr5:73082435
|
C | T | 3 | a0002c0002t0002g0033a0002c0002t0002g0037a0002c0002t0002g0059 | 3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2181-326C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082435 | ||||||
chr5:73082855
|
A | T | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2245+30A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73082855 | ||||||
chr5:73082876
|
AT | A | 96 | a0001c0001t0001g0162a0001c0001t0001g0199a0001c0003t0003g0099others(93): Show | 96 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2245+67delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73082876 | |||||
chr5:73082896
|
A | G | 1 | a0001c0003t0004g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2245+71A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73082896 | ||||||
chr5:73083009
|
G | C | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2245+184G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083009 | ||||||
chr5:73083021
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2245+196G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083021 | ||||||
chr5:73083036
|
A | G | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2245+211A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083036 | ||||||
chr5:73083055
|
T | G | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2245+230T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083055 | ||||||
chr5:73083086
|
A | G | 9 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2245+261A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083086 | ||||||
chr5:73083135
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2245+310C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083135 | ||||||
chr5:73083136
|
G | A | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2245+311G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083136 | ||||||
chr5:73083194
|
C | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2245+369C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083194 | ||||||
chr5:73083391
|
T | A | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2245+566T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083391 | ||||||
chr5:73083440
|
T | TAAGAAAC others(304): Show |
1 | a0001c0001t0015g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2245+624_2245+625i others(313): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73083440 | |||||
chr5:73083478
|
C | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2245+653C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083478 | ||||||
chr5:73083547
|
C | T | 2 | a0001c0003t0005g0107a0001c0003t0005g0108 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2245+722C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083547 | ||||||
chr5:73083614
|
C | T | 1 | a0001c0003t0011g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2245+789C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083614 | ||||||
chr5:73083615
|
G | C | 1 | a0003c0006t0005g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2245+790G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083615 | ||||||
chr5:73083619
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2245+794C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083619 | ||||||
chr5:73083892
|
C | CA | 17 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0130others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.2245+1087dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73083892 | |||||
chr5:73083892
|
CA | C | 92 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(89): Show | 92 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.2245+1087delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73083892 | |||||
chr5:73083898
|
A | T | 1 | a0001c0004t0003g0247 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+1073A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083898 | ||||||
chr5:73083914
|
C | G | 5 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2245+1089C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083914 | ||||||
chr5:73084127
|
T | C | 3 | a0002c0002t0002g0015a0002c0002t0002g0021a0002c0002t0002g0064 | 3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2245+1302T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084127 | ||||||
chr5:73084255
|
G | T | 3 | a0001c0001t0001g0131a0001c0003t0004g0093a0001c0003t0004g0094 | 3 | HG01261.hp2 HG02615.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2245+1430G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084255 | ||||||
chr5:73084395
|
A | T | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2245+1570A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084395 | ||||||
chr5:73084411
|
A | G | 217 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(214): Show | 217 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.2245+1586A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084411 | ||||||
chr5:73084486
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2245+1661G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084486 | ||||||
chr5:73084567
|
A | G | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2245+1742A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084567 | ||||||
chr5:73084575
|
A | G | 3 | a0001c0003t0003g0279a0001c0003t0003g0281a0004c0008t0003g0280 | 3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2245+1750A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084575 | ||||||
chr5:73084702
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2245+1877G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084702 | ||||||
chr5:73084758
|
A | G | 1 | a0002c0002t0002g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2245+1933A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084758 | ||||||
chr5:73085099
|
C | T | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.2245+2274C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085099 | ||||||
chr5:73085131
|
G | A | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2245+2306G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085131 | ||||||
chr5:73085143
|
G | C | 3 | a0001c0003t0008g0110a0001c0003t0008g0111a0001c0003t0008g0112 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2245+2318G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085143 | ||||||
chr5:73085194
|
C | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0168a0001c0001t0001g0170others(1): Show | 4 | NA18986.hp2 NA18992.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+2369C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085194 | ||||||
chr5:73085273
|
C | T | 99 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0003g0277others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2246-2316C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085273 | ||||||
chr5:73085511
|
A | AT | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2246-2076dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085511 | |||||
chr5:73085565
|
A | C | 28 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.2246-2024A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085565 | ||||||
chr5:73085777
|
A | AAAAT | 4 | a0002c0002t0002g0004a0002c0002t0002g0052a0002c0002t0002g0062others(1): Show | 4 | HG01169.hp1 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246-1765_2246-176 others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085777
|
AAAAT | A | 17 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0021others(14): Show | 17 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2246-1765_2246-176 others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085777
|
AAAATAAA others(1): Show |
A | 9 | a0001c0004t0003g0242a0002c0002t0002g0007a0002c0002t0002g0011others(6): Show | 9 | HG01099.hp1 HG02109.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.2246-1769_2246-176 others(12): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085777
|
AAAATAAA others(5): Show |
A | 61 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0133others(58): Show | 61 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2246-1773_2246-176 others(16): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085777
|
AAAATAAA others(9): Show |
A | 112 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0119others(109): Show | 112 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.2246-1777_2246-176 others(20): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085777
|
AAAATAAA others(13): Show |
A | 36 | a0001c0003t0004g0071a0001c0003t0004g0072a0001c0003t0004g0073others(33): Show | 36 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.2246-1781_2246-176 others(24): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085777
|
AAAATAAA others(21): Show |
A | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2246-1789_2246-176 others(32): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085777
|
AAAATAAA others(25): Show |
A | 6 | a0001c0003t0005g0002a0001c0003t0006g0101a0001c0003t0006g0102others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2246-1793_2246-176 others(36): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | |||||
chr5:73085781
|
T | C | 2 | a0002c0002t0002g0035a0002c0002t0002g0061 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2246-1808T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085781 | ||||||
chr5:73085783
|
AATAAATA others(11): Show |
A | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1804_2246-178 others(22): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085783 | |||||
chr5:73085802
|
A | T | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1787A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085802 | ||||||
chr5:73085818
|
A | T | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1771A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085818 | ||||||
chr5:73085972
|
A | G | 2 | a0001c0003t0010g0009a0001c0003t0010g0010 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2246-1617A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085972 | ||||||
chr5:73086040
|
T | G | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1549T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086040 | ||||||
chr5:73086095
|
C | T | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1494C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086095 | ||||||
chr5:73086096
|
T | A | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1493T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086096 | ||||||
chr5:73086138
|
C | A | 1 | a0001c0009t0001g0127 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2246-1451C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086138 | ||||||
chr5:73086608
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2246-981C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086608 | ||||||
chr5:73086654
|
G | T | 1 | a0002c0002t0002g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2246-935G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086654 | ||||||
chr5:73086670
|
A | T | 1 | a0001c0003t0003g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2246-919A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086670 | ||||||
chr5:73086745
|
G | T | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-844G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086745 | ||||||
chr5:73086751
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2246-838A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086751 | ||||||
chr5:73087167
|
A | G | 2 | a0001c0003t0005g0234a0001c0003t0005g0235 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2246-422A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73087167 | ||||||
chr5:73087362
|
C | A | 2 | a0001c0003t0003g0277a0001c0003t0003g0278 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2246-227C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73087362 | ||||||
chr5:73087775
|
T | C | 1 | a0001c0001t0013g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2410+22T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 25/25 | chr5 | 73087775 |