geneid | 2222 |
---|---|
ensemblid | ENSG00000079459.14 |
hgncid | 3629 |
symbol | FDFT1 |
name | farnesyl-diphosphate farnesyltransferase 1 |
refseq_nuc | NM_004462.5 |
refseq_prot | NP_004453.3 |
ensembl_nuc | ENST00000220584.9 |
ensembl_prot | ENSP00000220584.4 |
mane_status | MANE Select |
chr | chr8 |
start | 11802741 |
end | 11839298 |
strand | + |
ver | v1.2 |
region | chr8:11802741-11839298 |
region5000 | chr8:11797741-11844298 |
regionname0 | FDFT1_chr8_11802741_11839298 |
regionname5000 | FDFT1_chr8_11797741_11844298 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 417 | 434 | 97 | 75 | 199 | 15 | 46 | 156 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0002 | 0/0 | 417 | 11 | 0 | 5 | 1 | 1 | 4 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0003 | 0/0 | 417 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0004 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0005 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0006 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0007 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0008 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0009 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0010 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0011 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0012 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1254 | 166 | 34 | 39 | 55 | 9 | 29 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0002 | 0/0 | 1254 | 112 | 6 | 15 | 77 | 1 | 13 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0003 | 0/0 | 1254 | 67 | 4 | 2 | 60 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0004 | 0/1 | 1254 | 42 | 27 | 11 | 0 | 2 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0005 | 0/0 | 1254 | 12 | 5 | 3 | 0 | 2 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0006 | 0/0 | 1254 | 11 | 2 | 2 | 6 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0007 | 0/0 | 1254 | 6 | 0 | 5 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0008 | 0/0 | 1254 | 5 | 5 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0009 | 0/0 | 1254 | 5 | 0 | 0 | 1 | 0 | 4 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0010 | 1/0 | 1254 | 5 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0011 | 0/0 | 1254 | 4 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0012 | 0/0 | 1254 | 4 | 0 | 0 | 4 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0013 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0014 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0015 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0016 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0017 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0018 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0019 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0020 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0021 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0022 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0023 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0024 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0025 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0026 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0027 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0028 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0029 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
c0030 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 782 | 207 | 32 | 34 | 114 | 6 | 21 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0002 | 1/1 | 782 | 104 | 42 | 26 | 8 | 8 | 18 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0003 | 0/0 | 782 | 99 | 1 | 15 | 72 | 2 | 9 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0004 | 0/0 | 782 | 10 | 3 | 1 | 6 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0005 | 0/0 | 782 | 10 | 0 | 0 | 10 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0006 | 0/0 | 782 | 8 | 8 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0007 | 0/0 | 782 | 3 | 0 | 3 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0008 | 0/0 | 782 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0009 | 0/0 | 782 | 2 | 0 | 0 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0010 | 0/0 | 782 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0011 | 0/0 | 782 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0012 | 0/0 | 782 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0013 | 0/0 | 782 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0014 | 0/0 | 782 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0015 | 0/0 | 782 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0016 | 0/0 | 782 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0017 | 0/0 | 782 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
t0018 | 0/0 | 782 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0007 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0396 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0397 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1254 | 166 | 34 | 39 | 55 | 9 | 29 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0002 | 0/0 | 1254 | 112 | 6 | 15 | 77 | 1 | 13 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0003 | 0/0 | 1254 | 67 | 4 | 2 | 60 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0004 | 0/1 | 1254 | 42 | 27 | 11 | 0 | 2 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0005 | 0/0 | 1254 | 12 | 5 | 3 | 0 | 2 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0006 | 0/0 | 1254 | 11 | 2 | 2 | 6 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0008 | 0/0 | 1254 | 5 | 5 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0010 | 1/0 | 1254 | 5 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0011 | 0/0 | 1254 | 4 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0013 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0014 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0015 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0016 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0017 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0018 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0021 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0025 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0028 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0002c0007 | 0/0 | 1254 | 6 | 0 | 5 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0002c0009 | 0/0 | 1254 | 5 | 0 | 0 | 1 | 0 | 4 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0003c0012 | 0/0 | 1254 | 4 | 0 | 0 | 4 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0004c0029 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0005c0024 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0006c0022 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0007c0020 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0008c0019 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0009c0026 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0010c0027 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0011c0023 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0012c0030 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2035 | 110 | 16 | 27 | 45 | 5 | 17 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0002 | 0/0 | 2035 | 41 | 11 | 11 | 5 | 4 | 10 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0003 | 0/0 | 2035 | 4 | 0 | 0 | 3 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0004 | 0/0 | 2035 | 2 | 0 | 1 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0006 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0008 | 0/0 | 2035 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0009 | 0/0 | 2035 | 2 | 0 | 0 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0010 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0001t0011 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0002t0001 | 0/0 | 2035 | 15 | 2 | 2 | 7 | 0 | 4 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0002t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0002t0003 | 0/0 | 2035 | 80 | 0 | 13 | 58 | 1 | 8 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0002t0004 | 0/0 | 2035 | 6 | 3 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0002t0005 | 0/0 | 2035 | 9 | 0 | 0 | 9 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0002t0015 | 0/0 | 2035 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0003t0001 | 0/0 | 2035 | 50 | 0 | 0 | 50 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0003t0002 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0003t0003 | 0/0 | 2035 | 12 | 1 | 1 | 9 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0003t0004 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0003t0013 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0003t0014 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0004t0001 | 0/0 | 2035 | 6 | 6 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0004t0002 | 0/1 | 2035 | 26 | 14 | 8 | 0 | 2 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0004t0006 | 0/0 | 2035 | 6 | 6 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0004t0007 | 0/0 | 2035 | 3 | 0 | 3 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0004t0010 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0005t0001 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0005t0002 | 0/0 | 2035 | 8 | 1 | 3 | 0 | 2 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0005t0012 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0006t0001 | 0/0 | 2035 | 5 | 1 | 1 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0006t0002 | 0/0 | 2035 | 4 | 0 | 1 | 2 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0006t0005 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0006t0006 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0008t0001 | 0/0 | 2035 | 4 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0008t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0010t0002 | 1/0 | 2035 | 5 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0011t0002 | 0/0 | 2035 | 4 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0013t0002 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0014t0016 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0015t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0016t0002 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0017t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0018t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0021t0001 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0025t0003 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0001c0028t0002 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0002c0007t0001 | 0/0 | 2035 | 5 | 0 | 4 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0002c0007t0002 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0002c0009t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0002c0009t0002 | 0/0 | 2035 | 4 | 0 | 0 | 0 | 0 | 4 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0003c0012t0001 | 0/0 | 2035 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0003c0012t0018 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0004c0029t0003 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0005c0024t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0006c0022t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0007c0020t0002 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0008c0019t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0009c0026t0004 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0010c0027t0003 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0011c0023t0017 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
a0012c0030t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | copy fasta | chr8 | 11797741 | 11844298 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0001g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0002g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0006g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0009g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0011g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0003g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0004g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0005g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0002t0015g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0002g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0004g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0013g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0003t0014g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0001 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0002g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0007g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0004t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0005t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0006t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0008t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0008t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0008t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0008t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0008t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0010t0002g0007 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0010t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0010t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0011t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0011t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0013t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0013t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0014t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0015t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0016t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0017t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0018t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0021t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0025t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0001c0028t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0007t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0007t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0007t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0007t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0007t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0009t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0009t0002g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0002c0009t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0003c0012t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0003c0012t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0003c0012t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0003c0012t0018g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0004c0029t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0005c0024t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0006c0022t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0007c0020t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0008c0019t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0009c0026t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0010c0027t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0011c0023t0017g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
a0012c0030t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00140 | hp1 | a0001 | c0003 | t0003 | g0308 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0377 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0360 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00323 | hp1 | a0002 | c0007 | t0001 | g0034 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00323 | hp2 | a0001 | c0005 | t0002 | g0093 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0124 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00423 | hp2 | a0010 | c0027 | t0003 | g0276 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00438 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0390 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0270 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00597 | hp2 | a0003 | c0012 | t0018 | g0340 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00609 | hp2 | a0001 | c0002 | t0005 | g0241 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00639 | hp1 | a0001 | c0003 | t0014 | g0145 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00642 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00642 | hp2 | a0002 | c0007 | t0001 | g0352 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00673 | hp2 | a0001 | c0002 | t0005 | g0220 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0221 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00735 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0219 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00741 | hp1 | a0001 | c0004 | t0002 | g0398 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG00741 | hp2 | a0001 | c0028 | t0002 | g0373 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0203 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01070 | hp2 | a0001 | c0004 | t0007 | g0024 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01071 | hp1 | a0001 | c0004 | t0007 | g0024 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01081 | hp2 | a0002 | c0007 | t0001 | g0314 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0366 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01106 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01109 | hp2 | a0001 | c0004 | t0002 | g0170 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0225 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01168 | hp2 | a0001 | c0005 | t0002 | g0156 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01169 | hp2 | a0001 | c0005 | t0002 | g0155 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01175 | hp2 | a0001 | c0004 | t0007 | g0176 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0378 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01243 | hp1 | a0001 | c0005 | t0002 | g0160 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01255 | hp1 | a0001 | c0016 | t0002 | g0169 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01255 | hp2 | a0001 | c0006 | t0001 | g0356 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01256 | hp2 | a0002 | c0007 | t0002 | g0297 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01261 | hp1 | a0001 | c0004 | t0002 | g0006 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0240 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01358 | hp1 | a0001 | c0002 | t0003 | g0204 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0384 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01361 | hp2 | a0001 | c0006 | t0002 | g0185 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01496 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01496 | hp2 | a0001 | c0004 | t0002 | g0172 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0350 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0396 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0136 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0397 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01891 | hp1 | a0001 | c0008 | t0001 | g0082 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01891 | hp2 | a0001 | c0011 | t0002 | g0014 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01943 | hp1 | a0001 | c0003 | t0003 | g0354 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0267 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0268 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0230 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0337 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01993 | hp1 | a0002 | c0007 | t0001 | g0037 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02004 | hp1 | a0002 | c0007 | t0001 | g0034 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0053 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02071 | hp2 | a0001 | c0003 | t0003 | g0130 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02074 | hp1 | a0001 | c0002 | t0003 | g0266 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0103 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02080 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02083 | hp2 | a0004 | c0029 | t0003 | g0265 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02129 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02129 | hp2 | a0001 | c0002 | t0003 | g0253 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0402 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0399 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02135 | hp2 | a0001 | c0002 | t0005 | g0262 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02145 | hp2 | a0001 | c0013 | t0002 | g0180 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02165 | hp1 | a0001 | c0006 | t0001 | g0400 | EAS | CDX | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0237 | EAS | CDX | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0367 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0078 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02273 | hp2 | a0001 | c0025 | t0003 | g0054 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02280 | hp1 | a0001 | c0006 | t0001 | g0383 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0052 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02451 | hp1 | a0001 | c0005 | t0012 | g0039 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0077 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02523 | hp2 | a0001 | c0003 | t0001 | g0117 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02602 | hp2 | a0001 | c0002 | t0015 | g0223 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02615 | hp1 | a0001 | c0008 | t0002 | g0065 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02622 | hp1 | a0001 | c0004 | t0006 | g0072 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0042 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02630 | hp1 | a0001 | c0011 | t0002 | g0025 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02630 | hp2 | a0001 | c0021 | t0001 | g0098 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02647 | hp1 | a0001 | c0004 | t0002 | g0171 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02647 | hp2 | a0001 | c0005 | t0012 | g0048 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0191 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02717 | hp1 | a0001 | c0004 | t0002 | g0064 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02723 | hp1 | a0001 | c0005 | t0002 | g0158 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02723 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0189 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0018 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02809 | hp1 | a0001 | c0003 | t0002 | g0164 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02809 | hp2 | a0001 | c0010 | t0002 | g0007 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02818 | hp2 | a0001 | c0011 | t0002 | g0014 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02886 | hp1 | a0001 | c0015 | t0002 | g0181 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0403 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02895 | hp1 | a0001 | c0004 | t0006 | g0165 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0150 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02896 | hp1 | a0001 | c0010 | t0002 | g0100 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02897 | hp2 | a0001 | c0004 | t0006 | g0166 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02922 | hp2 | a0001 | c0004 | t0006 | g0075 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02965 | hp2 | a0001 | c0010 | t0002 | g0092 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02970 | hp1 | a0001 | c0013 | t0002 | g0177 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0066 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02976 | hp2 | a0001 | c0008 | t0001 | g0067 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0184 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0248 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03041 | hp1 | a0001 | c0003 | t0013 | g0405 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03041 | hp2 | a0001 | c0006 | t0006 | g0193 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03098 | hp1 | a0001 | c0017 | t0002 | g0040 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03098 | hp2 | a0001 | c0004 | t0002 | g0016 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03130 | hp1 | a0001 | c0008 | t0001 | g0080 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03130 | hp2 | a0001 | c0004 | t0002 | g0091 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03139 | hp1 | a0001 | c0014 | t0016 | g0073 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03139 | hp2 | a0001 | c0004 | t0002 | g0023 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0168 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0404 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03225 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03225 | hp2 | a0011 | c0023 | t0017 | g0041 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0382 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0363 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03453 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0070 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03490 | hp1 | a0002 | c0009 | t0002 | g0005 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03492 | hp1 | a0002 | c0009 | t0002 | g0005 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03540 | hp1 | a0001 | c0004 | t0002 | g0063 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0069 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03579 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0361 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03669 | hp2 | a0002 | c0009 | t0002 | g0005 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03704 | hp2 | a0001 | c0004 | t0002 | g0173 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03710 | hp1 | a0001 | c0002 | t0003 | g0029 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03710 | hp2 | a0001 | c0005 | t0002 | g0022 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03831 | hp2 | a0001 | c0002 | t0003 | g0192 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03927 | hp2 | a0001 | c0006 | t0002 | g0234 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03942 | hp1 | a0001 | c0002 | t0003 | g0260 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0388 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0385 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0222 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04204 | hp1 | a0001 | c0005 | t0002 | g0022 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0359 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0394 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG04228 | hp2 | a0002 | c0009 | t0002 | g0167 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18522 | hp1 | a0001 | c0008 | t0001 | g0081 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18522 | hp2 | a0001 | c0011 | t0002 | g0025 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18612 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0290 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0108 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0252 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0068 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18940 | hp1 | a0001 | c0003 | t0004 | g0386 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18940 | hp2 | a0001 | c0002 | t0003 | g0401 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18943 | hp2 | a0001 | c0002 | t0005 | g0245 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18944 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0355 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18948 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18949 | hp1 | a0001 | c0006 | t0005 | g0235 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18949 | hp2 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18952 | hp2 | a0001 | c0006 | t0001 | g0242 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18953 | hp1 | a0001 | c0006 | t0001 | g0216 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18953 | hp2 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18956 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18956 | hp2 | a0001 | c0018 | t0001 | g0372 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0395 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18959 | hp2 | a0001 | c0002 | t0003 | g0218 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0129 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18962 | hp1 | a0003 | c0012 | t0001 | g0353 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18963 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18965 | hp1 | a0003 | c0012 | t0001 | g0330 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18966 | hp2 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18968 | hp1 | a0001 | c0003 | t0003 | g0127 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18970 | hp1 | a0001 | c0002 | t0005 | g0249 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18970 | hp2 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18971 | hp1 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18972 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18972 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18973 | hp1 | a0002 | c0009 | t0001 | g0174 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0247 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18981 | hp1 | a0001 | c0002 | t0003 | g0278 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18982 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18982 | hp2 | a0008 | c0019 | t0001 | g0336 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18985 | hp2 | a0001 | c0002 | t0003 | g0257 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18986 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18987 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18987 | hp2 | a0007 | c0020 | t0002 | g0058 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18988 | hp2 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18992 | hp2 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18995 | hp1 | a0001 | c0003 | t0003 | g0271 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18997 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18997 | hp2 | a0001 | c0003 | t0001 | g0299 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0255 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19001 | hp1 | a0006 | c0022 | t0001 | g0381 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19002 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19004 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0277 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19006 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19007 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0392 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19010 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19010 | hp2 | a0001 | c0002 | t0004 | g0232 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19012 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0380 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19043 | hp2 | a0001 | c0004 | t0002 | g0178 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19054 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19055 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19055 | hp2 | a0009 | c0026 | t0004 | g0263 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0393 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19060 | hp1 | a0001 | c0002 | t0003 | g0231 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0391 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19062 | hp1 | a0001 | c0003 | t0003 | g0061 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19062 | hp2 | a0005 | c0024 | t0001 | g0113 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19063 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19063 | hp2 | a0001 | c0002 | t0003 | g0250 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19066 | hp2 | a0001 | c0006 | t0002 | g0261 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19068 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19070 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19075 | hp1 | a0012 | c0030 | t0001 | g0157 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19076 | hp1 | a0001 | c0002 | t0003 | g0254 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19076 | hp2 | a0003 | c0012 | t0001 | g0341 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0279 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19080 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0259 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19081 | hp1 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19081 | hp2 | a0001 | c0006 | t0002 | g0236 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19082 | hp1 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19085 | hp1 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0287 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19086 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0375 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19088 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0289 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19091 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0047 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA19240 | hp2 | a0001 | c0004 | t0002 | g0016 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20129 | hp1 | a0001 | c0004 | t0002 | g0175 | AFR | ASW | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20129 | hp2 | a0001 | c0004 | t0006 | g0074 | AFR | ASW | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20752 | hp1 | a0001 | c0004 | t0002 | g0001 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20752 | hp2 | a0001 | c0005 | t0002 | g0159 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20805 | hp1 | a0001 | c0004 | t0002 | g0006 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0224 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | GIH | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0029 | SAS | GIH | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0045 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02109 | hp2 | a0001 | c0010 | t0002 | g0007 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0044 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02559 | hp1 | a0001 | c0004 | t0002 | g0023 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0079 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
HG06807 | hp2 | a0001 | c0004 | t0006 | g0076 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18955 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0387 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0038 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
NA21309 | hp2 | a0001 | c0004 | t0010 | g0179 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0002 | g0006 | REF | REF | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
homoSapiens_grch38 | hp1 | a0001 | c0010 | t0002 | g0007 | REF | REF | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11808828
|
A | G | 2 | a0002a0012 | 12 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(9): Show |
missense_variant | MODERATE | c.134A>G | p.Lys45Arg | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/8 | 226/2035 | 134/1254 | 45/417 | chr8 | 11808828 | ||
chr8:11809729
|
C | G | 1 | a0004 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.260C>G | p.Thr87Ser | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/8 | 352/2035 | 260/1254 | 87/417 | chr8 | 11809729 | ||
chr8:11821790
|
C | T | 1 | a0005 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.422C>T | p.Thr141Ile | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/8 | 514/2035 | 422/1254 | 141/417 | chr8 | 11821790 | ||
chr8:11830287
|
C | T | 1 | a0006 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.746C>T | p.Pro249Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/8 | 838/2035 | 746/1254 | 249/417 | chr8 | 11830287 | ||
chr8:11830330
|
A | G | 1 | a0011 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.789A>G | p.Ile263Met | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/8 | 881/2035 | 789/1254 | 263/417 | chr8 | 11830330 | ||
chr8:11838422
|
C | G | 3 | a0003a0007a0012 | 6 | HG00597.hp2 NA18962.hp1 NA18965.hp1 others(3): Show |
missense_variant | MODERATE | c.1067C>G | p.Ser356Cys | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1159/2035 | 1067/1254 | 356/417 | chr8 | 11838422 | ||
chr8:11838431
|
C | G | 1 | a0008 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1076C>G | p.Thr359Arg | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1168/2035 | 1076/1254 | 359/417 | chr8 | 11838431 | ||
chr8:11838526
|
A | G | 1 | a0010 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1171A>G | p.Met391Val | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1263/2035 | 1171/1254 | 391/417 | chr8 | 11838526 | ||
chr8:11838606
|
C | G | 3 | a0003a0009a0012 | 6 | HG00597.hp2 NA18962.hp1 NA18965.hp1 others(3): Show |
missense_variant | MODERATE | c.1251C>G | p.His417Gln | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1343/2035 | 1251/1254 | 417/417 | chr8 | 11838606 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11802853
|
T | C | 8 | a0001c0004a0001c0008a0001c0011others(5): Show | 61 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(58): Show |
synonymous_variant | LOW | c.21T>C | p.Leu7Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 113/2035 | 21/1254 | 7/417 | chr8 | 11802853 | ||
chr8:11808875
|
C | T | 1 | a0001c0011 | 4 | HG01891.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.181C>T | p.Leu61Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/8 | 273/2035 | 181/1254 | 61/417 | chr8 | 11808875 | ||
chr8:11809670
|
C | T | 7 | a0001c0002a0001c0006a0001c0025others(4): Show | 128 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(125): Show |
synonymous_variant | LOW | c.201C>T | p.Asn67Asn | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/8 | 293/2035 | 201/1254 | 67/417 | chr8 | 11809670 | ||
chr8:11826113
|
T | C | 3 | a0001c0005a0001c0008a0001c0014 | 18 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
synonymous_variant | LOW | c.600T>C | p.Asp200Asp | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/8 | 692/2035 | 600/1254 | 200/417 | chr8 | 11826113 | ||
chr8:11826144
|
T | C | 26 | a0001c0001a0001c0002a0001c0003others(23): Show | 449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
synonymous_variant | LOW | c.631T>C | p.Leu211Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/8 | 723/2035 | 631/1254 | 211/417 | chr8 | 11826144 | ||
chr8:11830288
|
G | A | 1 | a0001c0025 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.747G>A | p.Pro249Pro | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/8 | 839/2035 | 747/1254 | 249/417 | chr8 | 11830288 | ||
chr8:11831592
|
A | G | 1 | a0001c0016 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.954A>G | p.Lys318Lys | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/8 | 1046/2035 | 954/1254 | 318/417 | chr8 | 11831592 | ||
chr8:11831608
|
C | T | 1 | a0001c0021 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.970C>T | p.Leu324Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/8 | 1062/2035 | 970/1254 | 324/417 | chr8 | 11831608 | ||
chr8:11831610
|
G | C | 8 | a0001c0002a0001c0003a0001c0025others(5): Show | 185 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(182): Show |
synonymous_variant | LOW | c.972G>C | p.Leu324Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/8 | 1064/2035 | 972/1254 | 324/417 | chr8 | 11831610 | ||
chr8:11838504
|
C | T | 1 | a0001c0018 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.1149C>T | p.Ser383Ser | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1241/2035 | 1149/1254 | 383/417 | chr8 | 11838504 | ||
chr8:11838552
|
G | A | 3 | a0001c0014a0001c0015a0001c0017 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.1197G>A | p.Gln399Gln | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1289/2035 | 1197/1254 | 399/417 | chr8 | 11838552 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11802753
|
C | G | 3 | a0001c0001t0008a0001c0001t0011a0001c0005t0012 | 7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-80C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | chr8 | 11802753 | ||||||
chr8:11802756
|
C | G | 1 | a0003c0012t0018 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 77 | chr8 | 11802756 | |||||
chr8:11802760
|
T | C | 1 | a0001c0004t0007 | 3 | HG01070.hp2 HG01071.hp1 HG01175.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 73 | chr8 | 11802760 | |||||
chr8:11802761
|
C | T | 1 | a0011c0023t0017 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 72 | chr8 | 11802761 | |||||
chr8:11838758
|
C | T | 2 | a0001c0001t0010a0001c0004t0010 | 2 | HG02622.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 149 | chr8 | 11838758 | |||||
chr8:11838830
|
A | G | 2 | a0001c0001t0010a0001c0004t0010 | 2 | HG02622.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*221A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 221 | chr8 | 11838830 | |||||
chr8:11838843
|
T | C | 24 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(21): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*234T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 234 | chr8 | 11838843 | |||||
chr8:11838885
|
C | T | 3 | a0001c0001t0006a0001c0004t0006a0001c0006t0006 | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*276C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 276 | chr8 | 11838885 | |||||
chr8:11838914
|
A | C | 2 | a0001c0002t0005a0001c0006t0005 | 10 | HG00609.hp2 HG00673.hp2 HG02135.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*305A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 305 | chr8 | 11838914 | |||||
chr8:11838931
|
C | T | 1 | a0001c0014t0016 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 322 | chr8 | 11838931 | |||||
chr8:11838974
|
A | G | 1 | a0001c0002t0015 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 365 | chr8 | 11838974 | |||||
chr8:11838983
|
A | C | 14 | a0001c0001t0003a0001c0001t0004a0001c0002t0003others(11): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*374A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 374 | chr8 | 11838983 | |||||
chr8:11839024
|
A | G | 1 | a0001c0003t0014 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 415 | chr8 | 11839024 | |||||
chr8:11839056
|
G | T | 2 | a0001c0001t0009a0001c0001t0011 | 4 | HG02109.hp1 HG02129.hp1 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*447G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 447 | chr8 | 11839056 | |||||
chr8:11839107
|
T | G | 1 | a0001c0003t0013 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 498 | chr8 | 11839107 | |||||
chr8:11839168
|
G | C | 3 | a0001c0001t0006a0001c0004t0006a0001c0006t0006 | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*559G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 559 | chr8 | 11839168 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11802956
|
C | T | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.99+25C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11802956 | ||||||
chr8:11802994
|
C | T | 1 | a0001c0001t0001g0403 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+63C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11802994 | ||||||
chr8:11803070
|
C | G | 4 | a0001c0002t0003g0399a0001c0002t0003g0401a0001c0002t0003g0402others(1): Show | 4 | HG02132.hp1 HG02135.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+139C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803070 | ||||||
chr8:11803084
|
C | T | 1 | a0001c0004t0002g0398 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.99+153C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803084 | ||||||
chr8:11803105
|
C | T | 239 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(236): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.99+174C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803105 | ||||||
chr8:11803135
|
C | T | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.99+204C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803135 | ||||||
chr8:11803146
|
C | G | 2 | a0001c0001t0001g0396a0001c0001t0001g0397 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.99+215C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803146 | ||||||
chr8:11803176
|
G | A | 1 | a0001c0003t0003g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+245G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803176 | ||||||
chr8:11803201
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+270C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803201 | ||||||
chr8:11803219
|
C | T | 3 | a0001c0004t0010g0179a0001c0013t0002g0180a0001c0015t0002g0181 | 3 | HG02145.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+288C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803219 | ||||||
chr8:11803223
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+292C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803223 | ||||||
chr8:11803248
|
C | T | 1 | a0001c0001t0001g0395 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.99+317C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803248 | ||||||
chr8:11803255
|
G | C | 122 | a0001c0001t0001g0207a0001c0001t0001g0212a0001c0001t0001g0213others(119): Show | 137 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.99+324G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803255 | ||||||
chr8:11803266
|
T | G | 1 | a0001c0005t0012g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+335T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803266 | ||||||
chr8:11803285
|
C | T | 1 | a0001c0001t0001g0394 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+354C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803285 | ||||||
chr8:11803407
|
C | T | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(237): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.99+476C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803407 | ||||||
chr8:11803428
|
G | T | 1 | a0001c0002t0003g0279 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.99+497G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803428 | ||||||
chr8:11803463
|
T | G | 1 | a0001c0003t0001g0049 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.99+532T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803463 | ||||||
chr8:11803567
|
A | G | 2 | a0001c0013t0002g0180a0001c0015t0002g0181 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.99+636A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803567 | ||||||
chr8:11803582
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99+651G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803582 | ||||||
chr8:11803657
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG02056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.99+726G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803657 | ||||||
chr8:11803689
|
C | G | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.99+758C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803689 | ||||||
chr8:11803713
|
A | T | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+782A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803713 | ||||||
chr8:11803751
|
G | A | 1 | a0001c0011t0002g0014 | 2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.99+820G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803751 | ||||||
chr8:11803784
|
T | G | 1 | a0001c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.99+853T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803784 | ||||||
chr8:11803837
|
A | G | 3 | a0001c0002t0003g0277a0001c0002t0003g0278a0010c0027t0003g0276 | 3 | HG00423.hp2 NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.99+906A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803837 | ||||||
chr8:11803855
|
G | A | 3 | a0001c0001t0010g0042a0001c0017t0002g0040a0011c0023t0017g0041 | 3 | HG02622.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.99+924G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803855 | ||||||
chr8:11803855
|
G | T | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+924G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803855 | ||||||
chr8:11803958
|
T | A | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1027T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803958 | ||||||
chr8:11803993
|
T | A | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+1062T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803993 | ||||||
chr8:11804057
|
G | C | 111 | a0001c0001t0001g0207a0001c0001t0001g0212a0001c0001t0001g0213others(108): Show | 124 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.99+1126G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804057 | ||||||
chr8:11804138
|
C | A | 3 | a0001c0001t0010g0042a0001c0017t0002g0040a0011c0023t0017g0041 | 3 | HG02622.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.99+1207C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804138 | ||||||
chr8:11804165
|
G | A | 406 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(403): Show | 455 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(452): Show |
intron_variant | MODIFIER | c.99+1234G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804165 | ||||||
chr8:11804221
|
C | G | 18 | a0001c0004t0002g0001a0001c0004t0002g0006a0001c0004t0002g0023others(15): Show | 30 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.99+1290C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804221 | ||||||
chr8:11804250
|
C | G | 2 | a0001c0004t0006g0165a0001c0004t0006g0166 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.99+1319C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804250 | ||||||
chr8:11804258
|
G | T | 1 | a0001c0002t0003g0270 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.99+1327G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804258 | ||||||
chr8:11804312
|
G | A | 1 | a0002c0009t0002g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+1381G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804312 | ||||||
chr8:11804411
|
G | A | 312 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(309): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.99+1480G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804411 | ||||||
chr8:11804412
|
T | A | 1 | a0001c0003t0001g0288 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+1481T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804412 | ||||||
chr8:11804586
|
T | A | 4 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | HG02738.hp1 HG03490.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+1655T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804586 | ||||||
chr8:11804600
|
C | CT | 54 | a0001c0001t0001g0395a0001c0001t0008g0043a0001c0002t0003g0186others(51): Show | 68 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+1690dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804600 | |||||
chr8:11804600
|
C | CTT | 241 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(238): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.99+1689_99+1690dup others(2): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804600 | |||||
chr8:11804600
|
C | CTTT | 20 | a0001c0001t0001g0385a0001c0001t0001g0387a0001c0001t0001g0389others(17): Show | 20 | HG00544.hp2 HG01361.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+1688_99+1690dup others(3): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804600 | |||||
chr8:11804639
|
T | C | 13 | a0001c0004t0001g0066a0001c0004t0001g0079a0001c0004t0002g0015others(10): Show | 15 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+1708T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804639 | ||||||
chr8:11804647
|
A | T | 3 | a0001c0004t0010g0179a0001c0013t0002g0180a0001c0015t0002g0181 | 3 | HG02145.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+1716A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804647 | ||||||
chr8:11804685
|
C | T | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99+1754C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804685 | ||||||
chr8:11804692
|
C | T | 1 | a0001c0001t0001g0382 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+1761C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804692 | ||||||
chr8:11804697
|
C | G | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1766C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804697 | ||||||
chr8:11804714
|
C | T | 1 | a0006c0022t0001g0381 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.99+1783C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804714 | ||||||
chr8:11804745
|
T | C | 4 | a0001c0001t0010g0042a0001c0004t0010g0179a0001c0017t0002g0040others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1814T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804745 | ||||||
chr8:11804746
|
A | G | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1815A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804746 | ||||||
chr8:11804800
|
G | C | 2 | a0001c0005t0002g0155a0001c0005t0002g0156 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.99+1869G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804800 | ||||||
chr8:11804816
|
T | C | 316 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(313): Show | 355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.99+1885T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804816 | ||||||
chr8:11804840
|
C | G | 7 | a0001c0001t0008g0043a0001c0001t0008g0046a0001c0001t0008g0047others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+1909C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804840 | ||||||
chr8:11804867
|
C | T | 11 | a0001c0001t0006g0380a0001c0004t0001g0071a0001c0004t0001g0077others(8): Show | 11 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+1936C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804867 | ||||||
chr8:11804868
|
C | A | 2 | a0001c0005t0002g0155a0001c0005t0002g0156 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.99+1937C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804868 | ||||||
chr8:11804875
|
C | T | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1944C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804875 | ||||||
chr8:11804908
|
C | CT | 24 | a0001c0001t0001g0376a0001c0001t0001g0377a0001c0001t0001g0378others(21): Show | 28 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+1994dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804908 | |||||
chr8:11804908
|
CT | C | 32 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(29): Show | 33 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+1994delT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804908 | |||||
chr8:11804908
|
CTT | C | 8 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(5): Show | 8 | HG02145.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+1993_99+1994del others(2): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804908 | |||||
chr8:11804925
|
T | G | 5 | a0001c0002t0003g0191a0001c0002t0003g0192a0001c0003t0001g0288others(2): Show | 6 | HG01891.hp2 HG02698.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1994T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804925 | ||||||
chr8:11804926
|
G | A | 5 | a0001c0002t0003g0191a0001c0002t0003g0192a0001c0003t0001g0288others(2): Show | 6 | HG01891.hp2 HG02698.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1995G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804926 | ||||||
chr8:11804927
|
A | AG | 268 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(265): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.99+2004dupG | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804927 | |||||
chr8:11804927
|
A | G | 7 | a0001c0001t0001g0374a0001c0002t0003g0191a0001c0002t0003g0192others(4): Show | 8 | HG01109.hp1 HG01891.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+1996A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804927 | ||||||
chr8:11804930
|
G | GT | 7 | a0001c0001t0008g0043a0001c0001t0008g0046a0001c0001t0008g0047others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+1999_99+2000ins others(1): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804930 | ||||||
chr8:11804930
|
G | T | 1 | a0001c0002t0001g0062 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.99+1999G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804930 | ||||||
chr8:11804939
|
C | T | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+2008C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804939 | ||||||
chr8:11804974
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.99+2043A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804974 | ||||||
chr8:11805039
|
C | T | 314 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(311): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.99+2108C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805039 | ||||||
chr8:11805054
|
C | T | 2 | a0001c0001t0001g0368a0001c0001t0001g0369 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.99+2123C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805054 | ||||||
chr8:11805075
|
A | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+2144A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805075 | ||||||
chr8:11805077
|
G | A | 5 | a0001c0001t0003g0010a0001c0001t0003g0272a0001c0003t0001g0273others(2): Show | 7 | HG00438.hp1 HG03654.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+2146G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805077 | ||||||
chr8:11805090
|
A | AT | 290 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(287): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.99+2166dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11805090 | |||||
chr8:11805114
|
G | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+2183G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805114 | ||||||
chr8:11805141
|
T | A | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+2210T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805141 | ||||||
chr8:11805142
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+2211C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805142 | ||||||
chr8:11805176
|
A | C | 1 | a0001c0003t0001g0152 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.99+2245A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805176 | ||||||
chr8:11805261
|
C | T | 405 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(402): Show | 454 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(451): Show |
intron_variant | MODIFIER | c.99+2330C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805261 | ||||||
chr8:11805323
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.99+2392T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805323 | ||||||
chr8:11805356
|
T | G | 13 | a0001c0002t0001g0196a0001c0002t0001g0200a0001c0002t0001g0201others(10): Show | 17 | NA18948.hp1 NA18950.hp1 NA18952.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+2425T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805356 | ||||||
chr8:11805363
|
A | G | 5 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(2): Show | 5 | NA18963.hp2 NA18971.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+2432A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805363 | ||||||
chr8:11805373
|
G | A | 1 | a0001c0003t0001g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+2442G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805373 | ||||||
chr8:11805376
|
G | A | 62 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(59): Show | 76 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+2445G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805376 | ||||||
chr8:11805426
|
A | G | 1 | a0001c0003t0003g0021 | 2 | NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.99+2495A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805426 | ||||||
chr8:11805453
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0002g0090a0001c0005t0001g0150 | 3 | HG02559.hp2 HG02895.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.99+2522C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805453 | ||||||
chr8:11805455
|
C | A | 1 | a0001c0003t0001g0049 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.99+2524C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805455 | ||||||
chr8:11805482
|
G | A | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.99+2551G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805482 | ||||||
chr8:11805490
|
T | C | 2 | a0001c0001t0002g0095a0001c0001t0002g0096 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.99+2559T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805490 | ||||||
chr8:11805504
|
T | C | 7 | a0001c0001t0008g0043a0001c0001t0008g0046a0001c0001t0008g0047others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+2573T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805504 | ||||||
chr8:11805512
|
G | C | 1 | a0001c0002t0003g0384 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99+2581G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805512 | ||||||
chr8:11805558
|
C | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+2627C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805558 | ||||||
chr8:11805566
|
C | T | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+2635C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805566 | ||||||
chr8:11805590
|
G | C | 1 | a0001c0001t0002g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+2659G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805590 | ||||||
chr8:11805600
|
T | C | 1 | a0001c0002t0003g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.99+2669T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805600 | ||||||
chr8:11805609
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0374 | 2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.99+2678G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805609 | ||||||
chr8:11805661
|
G | C | 237 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(234): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.99+2730G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805661 | ||||||
chr8:11805662
|
A | T | 304 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(301): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.99+2731A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805662 | ||||||
chr8:11805664
|
T | A | 304 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(301): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.99+2733T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805664 | ||||||
chr8:11805675
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99+2744G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805675 | ||||||
chr8:11805778
|
C | T | 43 | a0001c0001t0006g0380a0001c0004t0001g0066a0001c0004t0001g0070others(40): Show | 57 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+2847C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805778 | ||||||
chr8:11805885
|
G | T | 2 | a0001c0001t0001g0182a0001c0002t0003g0366 | 2 | HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-2909G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805885 | ||||||
chr8:11806025
|
T | C | 1 | a0001c0005t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-2769T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806025 | ||||||
chr8:11806038
|
T | C | 7 | a0001c0001t0008g0043a0001c0001t0008g0046a0001c0001t0008g0047others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-2756T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806038 | ||||||
chr8:11806075
|
C | A | 4 | a0001c0001t0010g0042a0001c0004t0010g0179a0001c0017t0002g0040others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2719C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806075 | ||||||
chr8:11806141
|
C | T | 6 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-2653C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806141 | ||||||
chr8:11806160
|
G | A | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-2634G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806160 | ||||||
chr8:11806202
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0147a0001c0001t0001g0148others(4): Show | 8 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-2592A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806202 | ||||||
chr8:11806224
|
C | T | 1 | a0001c0004t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100-2570C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806224 | ||||||
chr8:11806245
|
A | G | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.100-2549A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806245 | ||||||
chr8:11806254
|
C | T | 20 | a0001c0004t0001g0070a0001c0004t0002g0001a0001c0004t0002g0006others(17): Show | 32 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.100-2540C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806254 | ||||||
chr8:11806392
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100-2402T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806392 | ||||||
chr8:11806397
|
C | T | 1 | a0001c0002t0003g0270 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.100-2397C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806397 | ||||||
chr8:11806437
|
G | T | 1 | a0001c0001t0001g0365 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.100-2357G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806437 | ||||||
chr8:11806605
|
C | G | 1 | a0001c0002t0003g0384 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.100-2189C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806605 | ||||||
chr8:11806626
|
G | A | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-2168G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806626 | ||||||
chr8:11806767
|
A | G | 1 | a0001c0004t0002g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.100-2027A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806767 | ||||||
chr8:11806779
|
G | C | 6 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-2015G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806779 | ||||||
chr8:11806790
|
A | T | 7 | a0001c0001t0008g0043a0001c0001t0008g0046a0001c0001t0008g0047others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-2004A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806790 | ||||||
chr8:11806938
|
A | G | 1 | a0001c0001t0004g0258 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.100-1856A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806938 | ||||||
chr8:11807023
|
TACAAATA others(3): Show |
T | 245 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(242): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.100-1766_100-1757d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807023 | |||||
chr8:11807044
|
T | G | 1 | a0001c0002t0003g0204 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.100-1750T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807044 | ||||||
chr8:11807048
|
T | A | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.100-1746T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807048 | ||||||
chr8:11807072
|
G | A | 2 | a0001c0001t0011g0044a0001c0001t0011g0045 | 2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.100-1722G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807072 | ||||||
chr8:11807078
|
T | TGTTACCA others(18): Show |
1 | a0001c0005t0002g0022 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.100-1715_100-1691d others(27): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807078 | |||||
chr8:11807097
|
CTA | C | 238 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(235): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.100-1695_100-1694d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807097 | |||||
chr8:11807164
|
A | C | 2 | a0001c0013t0002g0180a0001c0015t0002g0181 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.100-1630A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807164 | ||||||
chr8:11807228
|
C | G | 1 | a0001c0002t0003g0257 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.100-1566C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807228 | ||||||
chr8:11807229
|
C | T | 257 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(254): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.100-1565C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807229 | ||||||
chr8:11807303
|
A | C | 1 | a0001c0003t0001g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.100-1491A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807303 | ||||||
chr8:11807309
|
C | G | 270 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(267): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.100-1485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807309 | ||||||
chr8:11807325
|
ATTTTTTA others(5): Show |
A | 270 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(267): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.100-1461_100-1450d others(14): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807325 | |||||
chr8:11807355
|
G | C | 2 | a0001c0003t0003g0038a0001c0021t0001g0098 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100-1439G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807355 | ||||||
chr8:11807359
|
C | G | 1 | a0001c0003t0014g0145 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-1435C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807359 | ||||||
chr8:11807386
|
T | C | 314 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(311): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.100-1408T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807386 | ||||||
chr8:11807393
|
G | T | 1 | a0001c0001t0001g0364 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100-1401G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807393 | ||||||
chr8:11807422
|
C | A | 1 | a0001c0001t0001g0294 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-1372C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807422 | ||||||
chr8:11807422
|
C | T | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-1372C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807422 | ||||||
chr8:11807443
|
G | A | 1 | a0001c0004t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100-1351G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807443 | ||||||
chr8:11807507
|
A | G | 319 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(316): Show | 358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.100-1287A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807507 | ||||||
chr8:11807511
|
CTG | C | 4 | a0001c0001t0010g0042a0001c0004t0010g0179a0001c0017t0002g0040others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-1280_100-1279d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807511 | |||||
chr8:11807514
|
T | G | 44 | a0001c0001t0006g0380a0001c0004t0001g0066a0001c0004t0001g0070others(41): Show | 58 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.100-1280T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807514 | ||||||
chr8:11807548
|
C | T | 1 | a0001c0002t0001g0256 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.100-1246C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807548 | ||||||
chr8:11807586
|
TA | T | 241 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(238): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.100-1202delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807586 | |||||
chr8:11807638
|
A | C | 1 | a0001c0005t0002g0160 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.100-1156A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807638 | ||||||
chr8:11807708
|
G | A | 241 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(238): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.100-1086G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807708 | ||||||
chr8:11807816
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.100-978T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807816 | ||||||
chr8:11807818
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.100-976G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807818 | ||||||
chr8:11807999
|
A | G | 1 | a0001c0002t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.100-795A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807999 | ||||||
chr8:11808003
|
G | T | 2 | a0001c0013t0002g0180a0001c0015t0002g0181 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.100-791G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808003 | ||||||
chr8:11808009
|
A | G | 315 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(312): Show | 354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.100-785A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808009 | ||||||
chr8:11808049
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.100-745G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808049 | ||||||
chr8:11808152
|
C | T | 264 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(261): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.100-642C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808152 | ||||||
chr8:11808166
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-628G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808166 | ||||||
chr8:11808195
|
C | T | 20 | a0001c0001t0002g0019a0001c0001t0002g0095a0001c0001t0002g0096others(17): Show | 21 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-599C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808195 | ||||||
chr8:11808296
|
C | T | 259 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(256): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.100-498C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808296 | ||||||
chr8:11808350
|
T | A | 14 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(11): Show | 14 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-444T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808350 | ||||||
chr8:11808399
|
G | T | 6 | a0001c0003t0001g0128a0001c0003t0001g0131a0001c0003t0003g0021others(3): Show | 7 | HG02071.hp2 HG02080.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-395G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808399 | ||||||
chr8:11808419
|
G | A | 3 | a0001c0004t0002g0001a0001c0004t0002g0173a0001c0004t0002g0398 | 7 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-375G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808419 | ||||||
chr8:11808444
|
C | G | 2 | a0001c0001t0002g0126a0001c0003t0002g0164 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100-350C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808444 | ||||||
chr8:11808450
|
C | T | 258 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(255): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.100-344C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808450 | ||||||
chr8:11808474
|
G | C | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.100-320G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808474 | ||||||
chr8:11808493
|
A | G | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-301A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808493 | ||||||
chr8:11808498
|
C | T | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-296C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808498 | ||||||
chr8:11808562
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-232G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808562 | ||||||
chr8:11808599
|
G | A | 1 | a0001c0005t0001g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-195G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808599 | ||||||
chr8:11808638
|
C | T | 1 | a0001c0001t0001g0362 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.100-156C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808638 | ||||||
chr8:11808647
|
G | T | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-147G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808647 | ||||||
chr8:11808649
|
C | G | 6 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-145C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808649 | ||||||
chr8:11808692
|
T | G | 1 | a0001c0003t0001g0205 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.100-102T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808692 | ||||||
chr8:11808709
|
G | GTCCCACT others(5): Show |
13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-57_100-46dupCA others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | |||||
chr8:11808709
|
G | GTCCCACT others(11): Show |
5 | a0001c0005t0002g0093a0001c0005t0002g0155a0001c0005t0002g0156others(2): Show | 5 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-63_100-46dupCA others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | |||||
chr8:11808709
|
G | GTCCCACT others(17): Show |
1 | a0001c0005t0002g0022 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.100-69_100-46dupCA others(22): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | |||||
chr8:11808709
|
GTCCCAC | G | 369 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(366): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.100-51_100-46delCA others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | |||||
chr8:11808709
|
GTCCCACT others(5): Show |
G | 8 | a0001c0001t0001g0361a0001c0001t0001g0392a0001c0002t0003g0255others(5): Show | 8 | HG02080.hp2 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-57_100-46delCA others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | |||||
chr8:11808709
|
GTCCCACT others(11): Show |
G | 3 | a0001c0001t0001g0020a0001c0001t0001g0148a0001c0001t0001g0149 | 4 | HG02257.hp1 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-63_100-46delCA others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | |||||
chr8:11808738
|
A | C | 9 | a0001c0004t0001g0071a0001c0004t0001g0077a0001c0004t0006g0072others(6): Show | 9 | HG02451.hp2 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-56A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808738 | ||||||
chr8:11808942
|
C | T | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(241): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.197+51C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11808942 | ||||||
chr8:11808991
|
C | A | 1 | a0001c0002t0003g0210 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.197+100C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11808991 | ||||||
chr8:11809015
|
A | C | 1 | a0001c0003t0001g0393 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.197+124A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809015 | ||||||
chr8:11809107
|
A | C | 70 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(67): Show | 83 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.197+216A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809107 | ||||||
chr8:11809107
|
A | G | 254 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(251): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.197+216A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809107 | ||||||
chr8:11809108
|
G | T | 1 | a0001c0002t0003g0384 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.197+217G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809108 | ||||||
chr8:11809109
|
G | T | 2 | a0001c0002t0003g0254a0001c0003t0001g0124 | 2 | HG00423.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.197+218G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809109 | ||||||
chr8:11809145
|
T | C | 23 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(20): Show | 23 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(20): Show |
intron_variant | MODIFIER | c.197+254T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809145 | ||||||
chr8:11809205
|
T | C | 1 | a0001c0001t0001g0385 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.197+314T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809205 | ||||||
chr8:11809220
|
A | G | 1 | a0001c0002t0001g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197+329A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809220 | ||||||
chr8:11809224
|
T | C | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.197+333T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809224 | ||||||
chr8:11809249
|
C | T | 17 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(14): Show | 17 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.197+358C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809249 | ||||||
chr8:11809259
|
C | G | 270 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(267): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.197+368C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809259 | ||||||
chr8:11809261
|
T | C | 34 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(31): Show | 47 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.197+370T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809261 | ||||||
chr8:11809282
|
A | C | 4 | a0001c0001t0001g0357a0001c0001t0001g0358a0001c0001t0001g0359others(1): Show | 4 | HG00280.hp2 HG01975.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-385A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809282 | ||||||
chr8:11809308
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.198-359A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809308 | ||||||
chr8:11809343
|
T | G | 2 | a0001c0004t0002g0091a0001c0013t0002g0177 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.198-324T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809343 | ||||||
chr8:11809466
|
A | T | 1 | a0001c0001t0001g0369 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198-201A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809466 | ||||||
chr8:11809518
|
C | A | 1 | a0001c0001t0001g0370 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198-149C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809518 | ||||||
chr8:11809535
|
G | T | 6 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-132G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809535 | ||||||
chr8:11809540
|
A | T | 2 | a0001c0004t0002g0091a0001c0013t0002g0177 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.198-127A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809540 | ||||||
chr8:11809594
|
G | C | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198-73G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809594 | ||||||
chr8:11809646
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.198-21A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809646 | ||||||
chr8:11809903
|
C | T | 9 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(6): Show | 9 | HG00733.hp2 HG02145.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+53C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11809903 | ||||||
chr8:11809976
|
G | A | 1 | a0001c0002t0003g0188 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.381+126G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11809976 | ||||||
chr8:11809987
|
C | T | 142 | a0001c0001t0002g0013a0001c0001t0002g0050a0001c0001t0002g0056others(139): Show | 157 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.381+137C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11809987 | ||||||
chr8:11810064
|
C | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0148a0001c0001t0001g0149 | 4 | HG02257.hp1 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+214C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810064 | ||||||
chr8:11810074
|
C | G | 1 | a0001c0001t0002g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+224C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810074 | ||||||
chr8:11810105
|
G | C | 1 | a0001c0004t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+255G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810105 | ||||||
chr8:11810107
|
GTAA | G | 124 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(121): Show | 135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.381+264_381+266del others(3): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810107 | |||||
chr8:11810114
|
T | C | 3 | a0001c0002t0003g0277a0001c0002t0003g0278a0010c0027t0003g0276 | 3 | HG00423.hp2 NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.381+264T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810114 | ||||||
chr8:11810130
|
G | A | 1 | a0001c0005t0002g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.381+280G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810130 | ||||||
chr8:11810172
|
G | C | 1 | a0001c0001t0001g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.381+322G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810172 | ||||||
chr8:11810191
|
TATTATC | T | 15 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(12): Show | 15 | HG00733.hp2 HG02145.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+343_381+348del others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810191 | |||||
chr8:11810193
|
T | C | 1 | a0002c0007t0002g0297 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.381+343T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810193 | ||||||
chr8:11810214
|
T | C | 13 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(10): Show | 13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.381+364T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810214 | ||||||
chr8:11810230
|
A | T | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.381+380A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810230 | ||||||
chr8:11810234
|
C | A | 1 | a0001c0001t0010g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.381+384C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810234 | ||||||
chr8:11810373
|
G | T | 1 | a0001c0002t0003g0188 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.381+523G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810373 | ||||||
chr8:11810386
|
C | T | 9 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(6): Show | 9 | HG00733.hp2 HG02145.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+536C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810386 | ||||||
chr8:11810510
|
A | C | 2 | a0001c0013t0002g0180a0001c0015t0002g0181 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.381+660A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810510 | ||||||
chr8:11810534
|
G | C | 1 | a0001c0002t0003g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.381+684G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810534 | ||||||
chr8:11810537
|
C | T | 1 | a0001c0003t0003g0354 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.381+687C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810537 | ||||||
chr8:11810563
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.381+713G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810563 | ||||||
chr8:11810588
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.381+738T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810588 | ||||||
chr8:11810644
|
T | C | 117 | a0001c0001t0001g0212a0001c0001t0001g0298a0001c0002t0001g0031others(114): Show | 130 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.381+794T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810644 | ||||||
chr8:11810655
|
G | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0057a0007c0020t0002g0058 | 3 | NA18939.hp2 NA18987.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.381+805G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810655 | ||||||
chr8:11810670
|
T | C | 7 | a0001c0002t0003g0215a0001c0002t0003g0217a0001c0002t0003g0218others(4): Show | 7 | HG00558.hp2 HG02074.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+820T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810670 | ||||||
chr8:11810693
|
A | G | 1 | a0011c0023t0017g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.381+843A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810693 | ||||||
chr8:11810718
|
C | T | 6 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+868C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810718 | ||||||
chr8:11810768
|
G | A | 6 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+918G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810768 | ||||||
chr8:11810854
|
G | C | 2 | a0001c0001t0001g0396a0001c0001t0001g0397 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.381+1004G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810854 | ||||||
chr8:11810878
|
G | C | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+1028G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810878 | ||||||
chr8:11810923
|
G | T | 1 | a0001c0003t0001g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.381+1073G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810923 | ||||||
chr8:11810933
|
T | TA | 12 | a0001c0002t0001g0202a0001c0002t0003g0183a0001c0002t0003g0199others(9): Show | 13 | HG01255.hp1 HG01361.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.381+1108dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | |||||
chr8:11810933
|
T | TAA | 98 | a0001c0001t0001g0298a0001c0002t0001g0031a0001c0002t0001g0055others(95): Show | 111 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.381+1107_381+1108d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | |||||
chr8:11810933
|
T | TAAA | 9 | a0001c0002t0002g0275a0001c0002t0003g0051a0001c0002t0003g0195others(6): Show | 9 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+1106_381+1108d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | |||||
chr8:11810933
|
TA | T | 163 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(160): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.381+1108delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | |||||
chr8:11810933
|
TAA | T | 73 | a0001c0001t0001g0037a0001c0001t0001g0207a0001c0001t0001g0282others(70): Show | 79 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.381+1107_381+1108d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | |||||
chr8:11811040
|
T | C | 1 | a0001c0004t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.381+1190T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811040 | ||||||
chr8:11811050
|
T | G | 47 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(44): Show | 60 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.381+1200T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811050 | ||||||
chr8:11811087
|
G | A | 1 | a0002c0007t0002g0297 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.381+1237G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811087 | ||||||
chr8:11811115
|
A | T | 1 | a0001c0003t0013g0405 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.381+1265A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811115 | ||||||
chr8:11811181
|
T | G | 1 | a0001c0003t0002g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381+1331T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811181 | ||||||
chr8:11811242
|
C | G | 11 | a0001c0004t0001g0066a0001c0004t0001g0079a0001c0004t0002g0015others(8): Show | 13 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+1392C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811242 | ||||||
chr8:11811258
|
C | T | 116 | a0001c0001t0001g0212a0001c0002t0001g0031a0001c0002t0001g0055others(113): Show | 129 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.381+1408C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811258 | ||||||
chr8:11811275
|
G | A | 3 | a0001c0001t0010g0042a0001c0004t0010g0179a0011c0023t0017g0041 | 3 | HG02622.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.381+1425G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811275 | ||||||
chr8:11811370
|
C | G | 2 | a0001c0008t0001g0067a0001c0008t0001g0082 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.381+1520C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811370 | ||||||
chr8:11811456
|
G | C | 1 | a0001c0004t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.381+1606G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811456 | ||||||
chr8:11811552
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.381+1702T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811552 | ||||||
chr8:11811617
|
T | A | 1 | a0001c0005t0002g0158 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+1767T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811617 | ||||||
chr8:11811757
|
C | A | 1 | a0001c0001t0001g0394 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.381+1907C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811757 | ||||||
chr8:11811855
|
G | A | 1 | a0001c0006t0002g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.381+2005G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811855 | ||||||
chr8:11811931
|
G | C | 114 | a0001c0001t0001g0212a0001c0002t0001g0031a0001c0002t0001g0055others(111): Show | 127 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.381+2081G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811931 | ||||||
chr8:11811944
|
A | G | 5 | a0001c0001t0001g0212a0001c0002t0003g0252a0001c0002t0003g0399others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+2094A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811944 | ||||||
chr8:11811976
|
C | G | 1 | a0001c0001t0002g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+2126C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811976 | ||||||
chr8:11812006
|
C | G | 1 | a0001c0001t0002g0144 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.381+2156C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812006 | ||||||
chr8:11812015
|
A | T | 1 | a0001c0002t0003g0257 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.381+2165A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812015 | ||||||
chr8:11812064
|
G | A | 1 | a0001c0001t0001g0349 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.381+2214G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812064 | ||||||
chr8:11812088
|
G | A | 1 | a0001c0002t0003g0221 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.381+2238G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812088 | ||||||
chr8:11812140
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.381+2290C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812140 | ||||||
chr8:11812153
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+2303G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812153 | ||||||
chr8:11812167
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.381+2317G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812167 | ||||||
chr8:11812222
|
C | T | 2 | a0001c0008t0001g0067a0001c0008t0001g0082 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.381+2372C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812222 | ||||||
chr8:11812237
|
T | G | 6 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(3): Show | 6 | HG00733.hp2 HG02738.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+2387T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812237 | ||||||
chr8:11812400
|
G | A | 1 | a0001c0003t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.381+2550G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812400 | ||||||
chr8:11812415
|
C | T | 2 | a0001c0006t0006g0193a0001c0028t0002g0373 | 2 | HG00741.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.381+2565C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812415 | ||||||
chr8:11812509
|
C | T | 1 | a0001c0002t0005g0249 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.381+2659C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812509 | ||||||
chr8:11812585
|
T | A | 1 | a0001c0018t0001g0372 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.381+2735T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812585 | ||||||
chr8:11812596
|
A | T | 54 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(51): Show | 67 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.381+2746A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812596 | ||||||
chr8:11812635
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.381+2785G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812635 | ||||||
chr8:11812677
|
T | C | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.381+2827T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812677 | ||||||
chr8:11812678
|
A | G | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.381+2828A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812678 | ||||||
chr8:11812679
|
G | T | 1 | a0001c0001t0001g0300 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+2829G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812679 | ||||||
chr8:11812709
|
C | G | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.381+2859C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812709 | ||||||
chr8:11812749
|
T | A | 1 | a0001c0003t0001g0105 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.381+2899T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812749 | ||||||
chr8:11812763
|
T | C | 55 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(52): Show | 68 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.381+2913T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812763 | ||||||
chr8:11812772
|
G | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 8 | HG01074.hp2 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+2922G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812772 | ||||||
chr8:11812781
|
T | C | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+2931T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812781 | ||||||
chr8:11812815
|
A | G | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.381+2965A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812815 | ||||||
chr8:11812874
|
G | T | 1 | a0001c0002t0003g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381+3024G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812874 | ||||||
chr8:11812886
|
G | A | 3 | a0001c0001t0010g0042a0001c0004t0010g0179a0011c0023t0017g0041 | 3 | HG02622.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.381+3036G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812886 | ||||||
chr8:11812889
|
A | G | 1 | a0001c0001t0001g0348 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.381+3039A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812889 | ||||||
chr8:11812911
|
A | G | 3 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202 | 3 | NA18971.hp2 NA18998.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.381+3061A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812911 | ||||||
chr8:11812931
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.381+3081C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812931 | ||||||
chr8:11812933
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.381+3083C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812933 | ||||||
chr8:11813020
|
T | C | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+3170T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813020 | ||||||
chr8:11813038
|
TCCAAGGC | T | 51 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(48): Show | 64 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.381+3189_381+3195d others(9): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813038 | ||||||
chr8:11813080
|
C | T | 1 | a0001c0002t0003g0247 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.381+3230C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813080 | ||||||
chr8:11813089
|
A | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+3239A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813089 | ||||||
chr8:11813149
|
G | A | 2 | a0001c0004t0001g0066a0001c0004t0001g0070 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.381+3299G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813149 | ||||||
chr8:11813157
|
A | T | 1 | a0001c0003t0002g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381+3307A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813157 | ||||||
chr8:11813197
|
C | G | 2 | a0001c0002t0003g0217a0001c0002t0003g0218 | 2 | NA18959.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.381+3347C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813197 | ||||||
chr8:11813275
|
T | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.381+3425T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813275 | ||||||
chr8:11813352
|
G | C | 1 | a0001c0001t0001g0351 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.381+3502G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813352 | ||||||
chr8:11813376
|
A | G | 6 | a0001c0004t0001g0079a0001c0008t0001g0067a0001c0008t0001g0080others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3526A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813376 | ||||||
chr8:11813423
|
C | T | 57 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(54): Show | 70 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.381+3573C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813423 | ||||||
chr8:11813440
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.381+3590A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813440 | ||||||
chr8:11813514
|
C | G | 1 | a0001c0002t0003g0246 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.381+3664C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813514 | ||||||
chr8:11813532
|
G | A | 123 | a0001c0001t0001g0306a0001c0001t0003g0010a0001c0001t0003g0272others(120): Show | 138 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.381+3682G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813532 | ||||||
chr8:11813554
|
A | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+3704A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813554 | ||||||
chr8:11813578
|
G | T | 1 | a0001c0003t0003g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.381+3728G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813578 | ||||||
chr8:11813599
|
C | T | 6 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0057others(3): Show | 6 | HG00733.hp2 HG02738.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3749C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813599 | ||||||
chr8:11813632
|
G | A | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+3782G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813632 | ||||||
chr8:11813637
|
A | G | 10 | a0001c0004t0001g0079a0001c0004t0002g0015a0001c0004t0002g0016others(7): Show | 12 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+3787A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813637 | ||||||
chr8:11813670
|
C | T | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+3820C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813670 | ||||||
chr8:11813711
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.381+3861G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813711 | ||||||
chr8:11813803
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+3953G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813803 | ||||||
chr8:11813853
|
T | C | 203 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(200): Show | 236 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.381+4003T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813853 | ||||||
chr8:11813886
|
G | A | 1 | a0001c0004t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+4036G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813886 | ||||||
chr8:11813892
|
A | G | 1 | a0001c0001t0001g0347 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.381+4042A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813892 | ||||||
chr8:11813906
|
CA | C | 36 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(33): Show | 49 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.381+4057delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813906 | ||||||
chr8:11813957
|
C | G | 7 | a0001c0005t0002g0022a0001c0005t0002g0093a0001c0005t0002g0155others(4): Show | 8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+4107C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813957 | ||||||
chr8:11814095
|
C | G | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381+4245C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814095 | ||||||
chr8:11814097
|
C | G | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.381+4247C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814097 | ||||||
chr8:11814150
|
A | G | 34 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(31): Show | 45 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+4300A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814150 | ||||||
chr8:11814280
|
G | A | 5 | a0001c0005t0002g0093a0001c0005t0002g0155a0001c0005t0002g0156others(2): Show | 5 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+4430G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814280 | ||||||
chr8:11814291
|
A | C | 2 | a0001c0001t0002g0126a0001c0003t0002g0164 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.381+4441A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814291 | ||||||
chr8:11814300
|
G | GT | 67 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(64): Show | 71 | HG00544.hp2 HG00639.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.381+4467dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814300 | |||||
chr8:11814300
|
G | GTT | 71 | a0001c0001t0001g0125a0001c0001t0001g0182a0001c0001t0001g0207others(68): Show | 80 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.381+4466_381+4467d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814300 | |||||
chr8:11814300
|
GT | G | 7 | a0001c0001t0001g0307a0001c0001t0001g0348a0001c0001t0001g0349others(4): Show | 9 | HG01169.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+4467delT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814300 | |||||
chr8:11814353
|
C | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.381+4503C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814353 | ||||||
chr8:11814380
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.381+4530G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814380 | ||||||
chr8:11814422
|
C | G | 1 | a0001c0001t0010g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.381+4572C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814422 | ||||||
chr8:11814423
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.381+4573T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814423 | ||||||
chr8:11814433
|
G | A | 2 | a0001c0006t0006g0193a0001c0028t0002g0373 | 2 | HG00741.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.381+4583G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814433 | ||||||
chr8:11814462
|
T | A | 3 | a0001c0001t0010g0042a0001c0004t0010g0179a0011c0023t0017g0041 | 3 | HG02622.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.381+4612T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814462 | ||||||
chr8:11814475
|
A | AC | 11 | a0001c0004t0001g0079a0001c0004t0002g0015a0001c0004t0002g0016others(8): Show | 13 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+4627dupC | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814475 | |||||
chr8:11814488
|
C | T | 1 | a0007c0020t0002g0058 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.381+4638C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814488 | ||||||
chr8:11814496
|
C | G | 1 | a0001c0004t0002g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.381+4646C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814496 | ||||||
chr8:11814502
|
T | C | 1 | a0001c0005t0002g0022 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.381+4652T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814502 | ||||||
chr8:11814519
|
C | T | 28 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(25): Show | 33 | HG00741.hp2 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.381+4669C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814519 | ||||||
chr8:11814714
|
C | G | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.381+4864C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814714 | ||||||
chr8:11814748
|
A | T | 1 | a0001c0002t0003g0051 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.381+4898A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814748 | ||||||
chr8:11814774
|
A | G | 1 | a0001c0002t0003g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.381+4924A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814774 | ||||||
chr8:11814805
|
GAT | G | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.381+4957_381+4958d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814805 | |||||
chr8:11814844
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381+4994T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814844 | ||||||
chr8:11814925
|
T | G | 5 | a0001c0004t0010g0179a0001c0006t0001g0383a0001c0013t0002g0180others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+5075T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814925 | ||||||
chr8:11814943
|
T | C | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+5093T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814943 | ||||||
chr8:11814972
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182 | 3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.381+5122A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814972 | ||||||
chr8:11815005
|
C | G | 2 | a0001c0001t0001g0292a0001c0001t0001g0374 | 2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.381+5155C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815005 | ||||||
chr8:11815020
|
C | T | 1 | a0009c0026t0004g0263 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.381+5170C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815020 | ||||||
chr8:11815041
|
C | A | 1 | a0001c0005t0012g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+5191C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815041 | ||||||
chr8:11815042
|
C | T | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.381+5192C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815042 | ||||||
chr8:11815061
|
C | G | 1 | a0001c0001t0002g0144 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.381+5211C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815061 | ||||||
chr8:11815065
|
G | A | 1 | a0001c0002t0003g0267 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.381+5215G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815065 | ||||||
chr8:11815089
|
A | C | 5 | a0001c0003t0001g0119a0001c0003t0001g0120a0001c0003t0001g0121others(2): Show | 5 | NA18962.hp2 NA18968.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+5239A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815089 | ||||||
chr8:11815114
|
T | C | 3 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0003t0003g0061 | 3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.381+5264T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815114 | ||||||
chr8:11815130
|
G | A | 2 | a0001c0004t0002g0023a0001c0004t0002g0168 | 3 | HG02559.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+5280G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815130 | ||||||
chr8:11815133
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+5283G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815133 | ||||||
chr8:11815150
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.381+5300A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815150 | ||||||
chr8:11815181
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.381+5331C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815181 | ||||||
chr8:11815203
|
C | G | 1 | a0001c0001t0001g0342 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.381+5353C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815203 | ||||||
chr8:11815211
|
A | G | 27 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(24): Show | 39 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.381+5361A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815211 | ||||||
chr8:11815263
|
C | A | 1 | a0001c0001t0001g0387 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.381+5413C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815263 | ||||||
chr8:11815364
|
T | C | 1 | a0001c0010t0002g0092 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5514T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815364 | ||||||
chr8:11815390
|
T | C | 27 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(24): Show | 39 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.381+5540T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815390 | ||||||
chr8:11815451
|
T | G | 24 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(21): Show | 36 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.381+5601T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815451 | ||||||
chr8:11815508
|
T | G | 1 | a0001c0002t0003g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381+5658T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815508 | ||||||
chr8:11815524
|
A | G | 58 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0001t0002g0083others(55): Show | 73 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.381+5674A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815524 | ||||||
chr8:11815546
|
T | A | 35 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(32): Show | 47 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.381+5696T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815546 | ||||||
chr8:11815659
|
T | A | 3 | a0001c0004t0007g0024a0001c0004t0007g0176a0001c0016t0002g0169 | 4 | HG01070.hp2 HG01071.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+5809T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815659 | ||||||
chr8:11815769
|
C | T | 2 | a0001c0001t0002g0126a0001c0003t0002g0164 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.381+5919C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815769 | ||||||
chr8:11815879
|
C | T | 5 | a0001c0001t0008g0043a0001c0001t0008g0046a0001c0001t0008g0047others(2): Show | 5 | HG02451.hp1 HG02647.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5871C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815879 | ||||||
chr8:11815907
|
A | G | 26 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(23): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.382-5843A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815907 | ||||||
chr8:11815923
|
T | C | 1 | a0007c0020t0002g0058 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.382-5827T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815923 | ||||||
chr8:11815970
|
G | A | 26 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0001t0002g0083others(23): Show | 29 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5780G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815970 | ||||||
chr8:11815976
|
T | C | 193 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(190): Show | 215 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.382-5774T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815976 | ||||||
chr8:11815992
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.382-5758C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815992 | ||||||
chr8:11815994
|
G | T | 4 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5756G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815994 | ||||||
chr8:11816081
|
C | T | 7 | a0001c0005t0002g0022a0001c0005t0002g0093a0001c0005t0002g0155others(4): Show | 8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-5669C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816081 | ||||||
chr8:11816092
|
C | G | 26 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0001t0002g0083others(23): Show | 29 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5658C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816092 | ||||||
chr8:11816143
|
G | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0391 | 3 | HG02056.hp2 NA19060.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.382-5607G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816143 | ||||||
chr8:11816191
|
T | C | 5 | a0001c0004t0002g0091a0001c0006t0001g0383a0001c0013t0002g0180others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5559T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816191 | ||||||
chr8:11816245
|
G | C | 8 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(5): Show | 8 | HG00544.hp2 NA18941.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-5505G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816245 | ||||||
chr8:11816310
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.382-5440C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816310 | ||||||
chr8:11816449
|
T | G | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0125others(1): Show | 4 | HG02970.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5301T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816449 | ||||||
chr8:11816476
|
G | C | 24 | a0001c0001t0001g0125a0001c0001t0002g0019a0001c0001t0002g0050others(21): Show | 25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.382-5274G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816476 | ||||||
chr8:11816480
|
C | T | 23 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(20): Show | 26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-5270C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816480 | ||||||
chr8:11816566
|
T | C | 23 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(20): Show | 26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-5184T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816566 | ||||||
chr8:11816568
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182 | 3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.382-5182T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816568 | ||||||
chr8:11816610
|
G | A | 3 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0003t0003g0061 | 3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.382-5140G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816610 | ||||||
chr8:11816628
|
C | G | 41 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(38): Show | 53 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.382-5122C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816628 | ||||||
chr8:11816683
|
G | A | 1 | a0001c0002t0003g0217 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.382-5067G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816683 | ||||||
chr8:11816689
|
G | C | 34 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(31): Show | 46 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.382-5061G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816689 | ||||||
chr8:11816749
|
T | G | 134 | a0001c0001t0001g0212a0001c0001t0001g0281a0001c0001t0001g0282others(131): Show | 147 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.382-5001T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816749 | ||||||
chr8:11816755
|
T | G | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0125others(1): Show | 4 | HG02970.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-4995T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816755 | ||||||
chr8:11816780
|
G | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-4970G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816780 | ||||||
chr8:11816782
|
G | C | 4 | a0001c0006t0001g0383a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4968G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816782 | ||||||
chr8:11816783
|
G | A | 3 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0003t0003g0061 | 3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.382-4967G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816783 | ||||||
chr8:11816792
|
A | G | 23 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(20): Show | 26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-4958A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816792 | ||||||
chr8:11816830
|
T | A | 1 | a0001c0001t0001g0306 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.382-4920T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816830 | ||||||
chr8:11816852
|
C | T | 4 | a0001c0006t0001g0383a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4898C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816852 | ||||||
chr8:11816871
|
C | A | 1 | a0001c0003t0001g0375 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.382-4879C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816871 | ||||||
chr8:11816904
|
G | T | 1 | a0001c0002t0005g0241 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.382-4846G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816904 | ||||||
chr8:11816963
|
G | T | 4 | a0001c0006t0001g0383a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4787G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816963 | ||||||
chr8:11816969
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-4781A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816969 | ||||||
chr8:11817039
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-4711G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817039 | ||||||
chr8:11817276
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.382-4474T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817276 | ||||||
chr8:11817284
|
A | C | 59 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(56): Show | 74 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.382-4466A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817284 | ||||||
chr8:11817388
|
TG | T | 4 | a0002c0007t0001g0034a0002c0007t0001g0314a0002c0007t0001g0352others(1): Show | 5 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-4361delG | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817388 | ||||||
chr8:11817446
|
G | T | 8 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(5): Show | 8 | HG00544.hp2 NA18941.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-4304G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817446 | ||||||
chr8:11817502
|
T | C | 10 | a0001c0002t0003g0184a0001c0002t0003g0189a0001c0002t0003g0203others(7): Show | 10 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-4248T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817502 | ||||||
chr8:11817685
|
T | A | 1 | a0001c0001t0001g0385 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.382-4065T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817685 | ||||||
chr8:11817694
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-4056G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817694 | ||||||
chr8:11817739
|
T | A | 265 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(262): Show | 303 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.382-4011T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817739 | ||||||
chr8:11817790
|
T | A | 1 | a0001c0002t0003g0028 | 2 | NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.382-3960T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817790 | ||||||
chr8:11817795
|
T | A | 3 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0003t0003g0061 | 3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.382-3955T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817795 | ||||||
chr8:11817809
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.382-3941C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817809 | ||||||
chr8:11817822
|
A | AT | 194 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(191): Show | 215 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.382-3917dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11817822 | |||||
chr8:11817822
|
A | ATT | 50 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(47): Show | 65 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.382-3918_382-3917d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11817822 | |||||
chr8:11817854
|
A | G | 266 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(263): Show | 305 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(302): Show |
intron_variant | MODIFIER | c.382-3896A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817854 | ||||||
chr8:11817907
|
T | A | 3 | a0001c0013t0002g0180a0001c0015t0002g0181a0011c0023t0017g0041 | 3 | HG02145.hp2 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.382-3843T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817907 | ||||||
chr8:11817936
|
C | G | 10 | a0001c0003t0002g0404a0001c0003t0013g0405a0001c0005t0001g0069others(7): Show | 11 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-3814C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817936 | ||||||
chr8:11818008
|
A | G | 4 | a0001c0004t0002g0091a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-3742A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818008 | ||||||
chr8:11818018
|
A | C | 1 | a0001c0002t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3732A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818018 | ||||||
chr8:11818022
|
A | T | 187 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(184): Show | 207 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.382-3728A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818022 | ||||||
chr8:11818089
|
T | A | 54 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(51): Show | 69 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.382-3661T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818089 | ||||||
chr8:11818161
|
A | T | 1 | a0001c0002t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3589A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818161 | ||||||
chr8:11818164
|
T | A | 1 | a0001c0002t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3586T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818164 | ||||||
chr8:11818166
|
T | C | 1 | a0001c0002t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3584T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818166 | ||||||
chr8:11818377
|
C | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0125others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.382-3373C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818377 | ||||||
chr8:11818391
|
G | A | 20 | a0001c0003t0002g0404a0001c0003t0013g0405a0001c0004t0001g0079others(17): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-3359G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818391 | ||||||
chr8:11818409
|
A | G | 1 | a0001c0004t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-3341A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818409 | ||||||
chr8:11818534
|
T | C | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.382-3216T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818534 | ||||||
chr8:11818554
|
G | GT | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182 | 3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.382-3195dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11818554 | |||||
chr8:11818561
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.382-3189T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818561 | ||||||
chr8:11818572
|
T | C | 4 | a0001c0004t0002g0091a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-3178T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818572 | ||||||
chr8:11818585
|
T | C | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.382-3165T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818585 | ||||||
chr8:11818609
|
T | A | 5 | a0001c0001t0011g0044a0001c0001t0011g0045a0001c0004t0001g0078others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-3141T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818609 | ||||||
chr8:11818667
|
G | C | 1 | a0001c0001t0002g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.382-3083G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818667 | ||||||
chr8:11818692
|
T | C | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | NA18957.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.382-3058T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818692 | ||||||
chr8:11818752
|
C | T | 1 | a0001c0006t0001g0356 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.382-2998C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818752 | ||||||
chr8:11818759
|
G | A | 4 | a0001c0004t0002g0091a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2991G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818759 | ||||||
chr8:11818762
|
G | A | 7 | a0001c0005t0002g0022a0001c0005t0002g0093a0001c0005t0002g0155others(4): Show | 8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-2988G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818762 | ||||||
chr8:11818800
|
T | C | 2 | a0001c0001t0001g0213a0001c0006t0001g0400 | 2 | HG00544.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.382-2950T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818800 | ||||||
chr8:11818802
|
T | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-2948T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818802 | ||||||
chr8:11818813
|
C | G | 4 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(1): Show | 4 | NA18971.hp2 NA18998.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2937C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818813 | ||||||
chr8:11818821
|
C | T | 1 | a0001c0005t0002g0158 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-2929C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818821 | ||||||
chr8:11818880
|
A | G | 4 | a0001c0004t0002g0091a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2870A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818880 | ||||||
chr8:11818886
|
T | G | 3 | a0001c0002t0003g0026a0001c0002t0003g0197a0001c0002t0003g0198 | 4 | NA18948.hp1 NA18966.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2864T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818886 | ||||||
chr8:11818920
|
A | G | 3 | a0003c0012t0001g0341a0003c0012t0018g0340a0012c0030t0001g0157 | 3 | HG00597.hp2 NA19075.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.382-2830A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818920 | ||||||
chr8:11818946
|
C | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(11): Show | 15 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.382-2804C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818946 | ||||||
chr8:11818955
|
C | G | 2 | a0001c0001t0001g0396a0001c0001t0001g0397 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.382-2795C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818955 | ||||||
chr8:11818984
|
C | T | 1 | a0001c0002t0003g0239 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.382-2766C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818984 | ||||||
chr8:11819004
|
C | G | 1 | a0001c0004t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.382-2746C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819004 | ||||||
chr8:11819010
|
T | G | 56 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(53): Show | 71 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.382-2740T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819010 | ||||||
chr8:11819025
|
G | T | 2 | a0001c0004t0002g0023a0001c0004t0002g0168 | 3 | HG02559.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.382-2725G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819025 | ||||||
chr8:11819057
|
A | G | 1 | a0001c0004t0002g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.382-2693A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819057 | ||||||
chr8:11819083
|
A | G | 238 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(235): Show | 272 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.382-2667A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819083 | ||||||
chr8:11819173
|
G | A | 52 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(49): Show | 67 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.382-2577G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819173 | ||||||
chr8:11819193
|
A | T | 238 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(235): Show | 272 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.382-2557A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819193 | ||||||
chr8:11819272
|
C | A | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.382-2478C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819272 | ||||||
chr8:11819350
|
A | G | 238 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(235): Show | 272 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.382-2400A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819350 | ||||||
chr8:11819396
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.382-2354C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819396 | ||||||
chr8:11819455
|
T | G | 53 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(50): Show | 68 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.382-2295T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819455 | ||||||
chr8:11819458
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.382-2292C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819458 | ||||||
chr8:11819460
|
TTCTG | T | 10 | a0001c0003t0002g0404a0001c0003t0013g0405a0001c0005t0001g0069others(7): Show | 11 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-2286_382-2283d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11819460 | |||||
chr8:11819485
|
C | A | 51 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(48): Show | 66 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.382-2265C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819485 | ||||||
chr8:11819487
|
A | G | 53 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(50): Show | 68 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.382-2263A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819487 | ||||||
chr8:11819516
|
C | G | 2 | a0001c0002t0001g0222a0001c0002t0001g0238 | 2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.382-2234C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819516 | ||||||
chr8:11819549
|
A | T | 1 | a0001c0001t0001g0339 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.382-2201A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819549 | ||||||
chr8:11819601
|
C | T | 24 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(21): Show | 36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.382-2149C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819601 | ||||||
chr8:11819612
|
A | G | 1 | a0001c0002t0003g0237 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.382-2138A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819612 | ||||||
chr8:11819615
|
C | A | 4 | a0001c0004t0002g0091a0001c0013t0002g0180a0001c0015t0002g0181others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2135C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819615 | ||||||
chr8:11819741
|
T | A | 171 | a0001c0001t0001g0207a0001c0001t0001g0212a0001c0001t0001g0306others(168): Show | 187 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.382-2009T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819741 | ||||||
chr8:11819781
|
C | G | 263 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(260): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.382-1969C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819781 | ||||||
chr8:11819791
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.382-1959G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819791 | ||||||
chr8:11819796
|
G | C | 210 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(207): Show | 232 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.382-1954G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819796 | ||||||
chr8:11819853
|
C | T | 1 | a0001c0002t0001g0196 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.382-1897C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819853 | ||||||
chr8:11819914
|
A | G | 1 | a0001c0001t0001g0378 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.382-1836A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819914 | ||||||
chr8:11819915
|
G | A | 1 | a0001c0001t0009g0018 | 2 | HG02129.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.382-1835G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819915 | ||||||
chr8:11819949
|
C | T | 253 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(250): Show | 288 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.382-1801C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819949 | ||||||
chr8:11819959
|
T | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-1791T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819959 | ||||||
chr8:11819963
|
T | G | 238 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0101others(235): Show | 272 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.382-1787T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819963 | ||||||
chr8:11819976
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.382-1774T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819976 | ||||||
chr8:11820009
|
G | C | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.382-1741G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820009 | ||||||
chr8:11820013
|
C | T | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-1737C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820013 | ||||||
chr8:11820015
|
T | C | 27 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(24): Show | 39 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.382-1735T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820015 | ||||||
chr8:11820054
|
T | C | 1 | a0001c0002t0003g0253 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.382-1696T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820054 | ||||||
chr8:11820104
|
G | T | 1 | a0001c0005t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.382-1646G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820104 | ||||||
chr8:11820131
|
G | A | 1 | a0001c0001t0001g0394 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.382-1619G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820131 | ||||||
chr8:11820135
|
A | C | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(110): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.382-1615A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820135 | ||||||
chr8:11820142
|
A | G | 8 | a0001c0005t0001g0069a0001c0005t0002g0022a0001c0005t0002g0093others(5): Show | 9 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-1608A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820142 | ||||||
chr8:11820215
|
G | C | 2 | a0001c0002t0001g0222a0001c0002t0001g0238 | 2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.382-1535G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820215 | ||||||
chr8:11820241
|
A | G | 6 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0194others(3): Show | 6 | NA18939.hp2 NA18950.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-1509A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820241 | ||||||
chr8:11820265
|
C | G | 7 | a0001c0005t0002g0022a0001c0005t0002g0093a0001c0005t0002g0155others(4): Show | 8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-1485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820265 | ||||||
chr8:11820294
|
C | A | 3 | a0001c0003t0002g0404a0001c0003t0013g0405a0001c0005t0001g0069 | 3 | HG03041.hp1 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-1456C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820294 | ||||||
chr8:11820296
|
T | A | 56 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0147others(53): Show | 69 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.382-1454T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820296 | ||||||
chr8:11820396
|
A | C | 31 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0125others(28): Show | 34 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.382-1354A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820396 | ||||||
chr8:11820419
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182 | 3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.382-1331C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820419 | ||||||
chr8:11820456
|
A | C | 1 | a0001c0003t0003g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.382-1294A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820456 | ||||||
chr8:11820470
|
G | T | 1 | a0001c0002t0003g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382-1280G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820470 | ||||||
chr8:11820471
|
G | T | 2 | a0001c0013t0002g0180a0011c0023t0017g0041 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.382-1279G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820471 | ||||||
chr8:11820481
|
TTGCTGAG others(1): Show |
T | 195 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(192): Show | 215 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.382-1265_382-1258d others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11820481 | |||||
chr8:11820493
|
G | A | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-1257G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820493 | ||||||
chr8:11820558
|
C | G | 2 | a0001c0001t0001g0338a0001c0001t0001g0378 | 2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.382-1192C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820558 | ||||||
chr8:11820658
|
G | A | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.382-1092G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820658 | ||||||
chr8:11820665
|
G | A | 2 | a0001c0001t0001g0347a0001c0001t0001g0379 | 2 | NA19057.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.382-1085G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820665 | ||||||
chr8:11820712
|
C | A | 1 | a0001c0001t0001g0316 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.382-1038C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820712 | ||||||
chr8:11820766
|
A | G | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-984A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820766 | ||||||
chr8:11820776
|
G | A | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.382-974G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820776 | ||||||
chr8:11820806
|
C | A | 1 | a0001c0001t0011g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-944C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820806 | ||||||
chr8:11820878
|
C | G | 1 | a0001c0002t0001g0201 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.382-872C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820878 | ||||||
chr8:11820895
|
G | A | 262 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(259): Show | 298 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.382-855G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820895 | ||||||
chr8:11820938
|
C | A | 1 | a0001c0004t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-812C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820938 | ||||||
chr8:11820992
|
A | G | 255 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(252): Show | 291 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.382-758A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820992 | ||||||
chr8:11820996
|
C | G | 1 | a0001c0001t0011g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-754C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820996 | ||||||
chr8:11821055
|
C | G | 7 | a0001c0005t0002g0022a0001c0005t0002g0093a0001c0005t0002g0155others(4): Show | 8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-695C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821055 | ||||||
chr8:11821064
|
T | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.382-686T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821064 | ||||||
chr8:11821082
|
T | A | 1 | a0001c0001t0002g0059 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.382-668T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821082 | ||||||
chr8:11821159
|
A | C | 255 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(252): Show | 291 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.382-591A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821159 | ||||||
chr8:11821190
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.382-560A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821190 | ||||||
chr8:11821208
|
G | C | 3 | a0001c0001t0001g0343a0001c0001t0001g0396a0001c0001t0001g0397 | 3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.382-542G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821208 | ||||||
chr8:11821235
|
G | C | 1 | a0001c0003t0003g0354 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.382-515G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821235 | ||||||
chr8:11821315
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.382-435G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821315 | ||||||
chr8:11821420
|
A | C | 9 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(6): Show | 11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-330A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821420 | ||||||
chr8:11821523
|
G | A | 1 | a0001c0002t0003g0259 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.382-227G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821523 | ||||||
chr8:11821608
|
C | G | 1 | a0001c0004t0006g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.382-142C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821608 | ||||||
chr8:11821648
|
C | T | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-102C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821648 | ||||||
chr8:11821668
|
C | T | 9 | a0001c0001t0002g0144a0001c0004t0002g0001a0001c0004t0002g0006others(6): Show | 16 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-82C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821668 | ||||||
chr8:11821728
|
G | C | 8 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(5): Show | 8 | HG00544.hp2 NA18941.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-22G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821728 | ||||||
chr8:11821735
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.382-15C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821735 | ||||||
chr8:11821936
|
A | G | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510+58A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11821936 | ||||||
chr8:11821955
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+77G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11821955 | ||||||
chr8:11821963
|
G | A | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.510+85G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11821963 | ||||||
chr8:11822022
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+144C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822022 | ||||||
chr8:11822049
|
C | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0298 | 2 | HG02015.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.510+171C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822049 | ||||||
chr8:11822056
|
A | C | 1 | a0001c0006t0005g0235 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.510+178A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822056 | ||||||
chr8:11822173
|
G | C | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.510+295G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822173 | ||||||
chr8:11822201
|
G | T | 9 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(6): Show | 11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+323G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822201 | ||||||
chr8:11822265
|
T | A | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+387T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822265 | ||||||
chr8:11822272
|
CA | C | 9 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(6): Show | 11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+395delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822272 | ||||||
chr8:11822274
|
G | A | 35 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(32): Show | 47 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.510+396G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822274 | ||||||
chr8:11822284
|
G | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+406G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822284 | ||||||
chr8:11822326
|
C | T | 1 | a0001c0005t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.510+448C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822326 | ||||||
chr8:11822331
|
C | CT | 37 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(34): Show | 49 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.510+456dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11822331 | |||||
chr8:11822494
|
A | G | 2 | a0001c0004t0002g0063a0001c0004t0002g0064 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.510+616A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822494 | ||||||
chr8:11822519
|
A | G | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510+641A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822519 | ||||||
chr8:11822608
|
G | A | 2 | a0001c0013t0002g0180a0011c0023t0017g0041 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.510+730G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822608 | ||||||
chr8:11822625
|
G | GC | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.510+748dupC | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11822625 | |||||
chr8:11822639
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+761C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822639 | ||||||
chr8:11822769
|
T | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+891T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822769 | ||||||
chr8:11822793
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.510+915G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822793 | ||||||
chr8:11822828
|
G | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+950G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822828 | ||||||
chr8:11822897
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.510+1019T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822897 | ||||||
chr8:11822959
|
A | T | 55 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(52): Show | 70 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.510+1081A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822959 | ||||||
chr8:11822966
|
A | T | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510+1088A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822966 | ||||||
chr8:11823001
|
C | T | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+1123C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823001 | ||||||
chr8:11823026
|
C | T | 194 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(191): Show | 214 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.510+1148C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823026 | ||||||
chr8:11823032
|
G | A | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1154G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823032 | ||||||
chr8:11823101
|
A | C | 2 | a0001c0004t0006g0165a0001c0004t0006g0166 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.510+1223A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823101 | ||||||
chr8:11823160
|
T | A | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1282T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823160 | ||||||
chr8:11823161
|
G | T | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+1283G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823161 | ||||||
chr8:11823193
|
CAGTCCTC others(28): Show |
C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1317_510+1351d others(37): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11823193 | |||||
chr8:11823210
|
C | T | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.510+1332C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823210 | ||||||
chr8:11823236
|
T | A | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1358T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823236 | ||||||
chr8:11823250
|
T | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1372T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823250 | ||||||
chr8:11823251
|
T | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1373T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823251 | ||||||
chr8:11823254
|
A | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1376A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823254 | ||||||
chr8:11823255
|
A | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1377A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823255 | ||||||
chr8:11823256
|
G | GGTCCCCC others(85): Show |
1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1379_510+1380i others(94): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11823256 | |||||
chr8:11823260
|
T | G | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1382T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823260 | ||||||
chr8:11823377
|
C | G | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1499C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823377 | ||||||
chr8:11823541
|
G | C | 1 | a0001c0003t0001g0111 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.510+1663G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823541 | ||||||
chr8:11823543
|
T | C | 9 | a0001c0002t0003g0226a0001c0002t0003g0252a0001c0002t0003g0277others(6): Show | 9 | HG00423.hp2 HG02132.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1665T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823543 | ||||||
chr8:11823623
|
G | C | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510+1745G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823623 | ||||||
chr8:11823626
|
A | T | 1 | a0001c0004t0006g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510+1748A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823626 | ||||||
chr8:11823655
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+1777C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823655 | ||||||
chr8:11823672
|
A | G | 2 | a0001c0003t0003g0021a0001c0003t0003g0127 | 3 | NA18968.hp1 NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.510+1794A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823672 | ||||||
chr8:11823694
|
T | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1816T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823694 | ||||||
chr8:11823737
|
A | G | 110 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(107): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.510+1859A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823737 | ||||||
chr8:11823758
|
T | A | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1880T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823758 | ||||||
chr8:11823805
|
A | G | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+1927A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823805 | ||||||
chr8:11823831
|
C | T | 9 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(6): Show | 11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+1953C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823831 | ||||||
chr8:11823837
|
G | T | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.510+1959G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823837 | ||||||
chr8:11823844
|
A | C | 1 | a0001c0001t0001g0343 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.510+1966A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823844 | ||||||
chr8:11823879
|
G | A | 29 | a0001c0001t0001g0125a0001c0001t0002g0087a0001c0001t0002g0088others(26): Show | 41 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.510+2001G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823879 | ||||||
chr8:11823883
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.510+2005A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823883 | ||||||
chr8:11823943
|
A | T | 24 | a0001c0001t0010g0042a0001c0004t0002g0015a0001c0004t0002g0016others(21): Show | 27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.510+2065A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823943 | ||||||
chr8:11823946
|
G | C | 1 | a0001c0001t0001g0318 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.510+2068G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823946 | ||||||
chr8:11823956
|
G | A | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.511-2068G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823956 | ||||||
chr8:11824007
|
G | C | 1 | a0001c0003t0001g0273 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.511-2017G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824007 | ||||||
chr8:11824027
|
G | C | 1 | a0001c0005t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-1997G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824027 | ||||||
chr8:11824028
|
C | A | 1 | a0001c0005t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-1996C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824028 | ||||||
chr8:11824078
|
G | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-1946G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824078 | ||||||
chr8:11824089
|
T | C | 1 | a0001c0002t0003g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.511-1935T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824089 | ||||||
chr8:11824106
|
C | G | 2 | a0001c0013t0002g0180a0011c0023t0017g0041 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.511-1918C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824106 | ||||||
chr8:11824227
|
T | TA | 9 | a0001c0005t0001g0069a0001c0005t0002g0022a0001c0005t0002g0093others(6): Show | 10 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-1795dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11824227 | |||||
chr8:11824304
|
A | C | 1 | a0001c0002t0003g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.511-1720A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824304 | ||||||
chr8:11824316
|
C | T | 258 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(255): Show | 295 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.511-1708C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824316 | ||||||
chr8:11824329
|
T | C | 180 | a0001c0001t0001g0283a0001c0001t0001g0291a0001c0001t0001g0317others(177): Show | 199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.511-1695T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824329 | ||||||
chr8:11824385
|
C | G | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02738.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.511-1639C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824385 | ||||||
chr8:11824402
|
A | G | 9 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(6): Show | 11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-1622A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824402 | ||||||
chr8:11824482
|
A | T | 1 | a0001c0006t0005g0235 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.511-1542A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824482 | ||||||
chr8:11824484
|
C | T | 17 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(14): Show | 18 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.511-1540C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824484 | ||||||
chr8:11824541
|
C | T | 1 | a0001c0021t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.511-1483C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824541 | ||||||
chr8:11824606
|
T | TC | 141 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(138): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.511-1417dupC | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11824606 | |||||
chr8:11824638
|
G | C | 2 | a0001c0001t0001g0396a0001c0001t0001g0397 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.511-1386G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824638 | ||||||
chr8:11824659
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-1365C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824659 | ||||||
chr8:11824664
|
T | C | 1 | a0001c0005t0012g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.511-1360T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824664 | ||||||
chr8:11824738
|
CTGT | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-1275_511-1273d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11824738 | |||||
chr8:11824758
|
C | T | 174 | a0001c0001t0001g0317a0001c0001t0001g0335a0001c0001t0001g0390others(171): Show | 191 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.511-1266C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824758 | ||||||
chr8:11824767
|
A | G | 1 | a0001c0005t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-1257A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824767 | ||||||
chr8:11824794
|
G | T | 1 | a0001c0002t0001g0196 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.511-1230G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824794 | ||||||
chr8:11824796
|
C | T | 2 | a0001c0001t0002g0126a0001c0003t0002g0164 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.511-1228C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824796 | ||||||
chr8:11824797
|
G | A | 2 | a0001c0002t0003g0248a0001c0002t0003g0290 | 2 | HG03017.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.511-1227G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824797 | ||||||
chr8:11824821
|
C | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(5): Show | 10 | HG02258.hp1 HG02486.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-1203C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824821 | ||||||
chr8:11824837
|
G | A | 1 | a0001c0002t0003g0204 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.511-1187G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824837 | ||||||
chr8:11824909
|
G | C | 9 | a0001c0001t0002g0144a0001c0004t0002g0001a0001c0004t0002g0006others(6): Show | 16 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-1115G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824909 | ||||||
chr8:11824936
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.511-1088C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824936 | ||||||
chr8:11824937
|
G | T | 7 | a0001c0004t0006g0072a0001c0004t0006g0074a0001c0004t0006g0075others(4): Show | 7 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-1087G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824937 | ||||||
chr8:11824939
|
C | G | 171 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(168): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.511-1085C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824939 | ||||||
chr8:11824967
|
T | C | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(222): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.511-1057T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824967 | ||||||
chr8:11824968
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.511-1056C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824968 | ||||||
chr8:11825047
|
T | C | 15 | a0001c0005t0001g0069a0001c0005t0002g0022a0001c0005t0002g0093others(12): Show | 16 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.511-977T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825047 | ||||||
chr8:11825057
|
C | A | 224 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(221): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.511-967C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825057 | ||||||
chr8:11825097
|
A | G | 1 | a0001c0002t0003g0290 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.511-927A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825097 | ||||||
chr8:11825142
|
G | C | 1 | a0001c0006t0002g0261 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.511-882G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825142 | ||||||
chr8:11825146
|
A | G | 1 | a0001c0004t0002g0064 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.511-878A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825146 | ||||||
chr8:11825161
|
A | G | 6 | a0001c0001t0010g0042a0001c0004t0002g0015a0001c0004t0002g0016others(3): Show | 8 | HG02622.hp2 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-863A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825161 | ||||||
chr8:11825189
|
C | T | 4 | a0001c0001t0001g0333a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG00597.hp1 HG03831.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-835C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825189 | ||||||
chr8:11825213
|
T | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-811T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825213 | ||||||
chr8:11825262
|
G | C | 192 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(189): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.511-762G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825262 | ||||||
chr8:11825263
|
C | T | 6 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0118others(3): Show | 6 | HG02129.hp2 NA18939.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-761C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825263 | ||||||
chr8:11825280
|
G | T | 1 | a0001c0001t0001g0332 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.511-744G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825280 | ||||||
chr8:11825349
|
G | C | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.511-675G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825349 | ||||||
chr8:11825369
|
C | G | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-655C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825369 | ||||||
chr8:11825369
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.511-655C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825369 | ||||||
chr8:11825392
|
T | A | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.511-632T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825392 | ||||||
chr8:11825405
|
G | C | 3 | a0001c0002t0003g0227a0001c0002t0003g0228a0001c0002t0005g0249 | 3 | HG02080.hp1 NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.511-619G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825405 | ||||||
chr8:11825431
|
T | C | 1 | a0001c0002t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.511-593T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825431 | ||||||
chr8:11825501
|
G | C | 401 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(398): Show | 450 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(447): Show |
intron_variant | MODIFIER | c.511-523G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825501 | ||||||
chr8:11825539
|
CA | C | 321 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(318): Show | 354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.511-464delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11825539 | |||||
chr8:11825539
|
CAA | C | 43 | a0001c0001t0001g0379a0001c0001t0001g0385a0001c0001t0001g0394others(40): Show | 54 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.511-465_511-464del others(2): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11825539 | |||||
chr8:11825560
|
A | C | 1 | a0001c0004t0002g0064 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.511-464A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825560 | ||||||
chr8:11825584
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.511-440G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825584 | ||||||
chr8:11825601
|
C | A | 1 | a0001c0002t0003g0270 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.511-423C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825601 | ||||||
chr8:11825635
|
T | C | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-389T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825635 | ||||||
chr8:11825655
|
C | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-369C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825655 | ||||||
chr8:11825685
|
T | A | 1 | a0001c0001t0002g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.511-339T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825685 | ||||||
chr8:11825686
|
C | A | 1 | a0001c0001t0002g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.511-338C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825686 | ||||||
chr8:11825686
|
C | CA | 353 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(350): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.511-328dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11825686 | |||||
chr8:11825697
|
T | A | 26 | a0001c0001t0001g0125a0001c0001t0002g0013a0001c0001t0002g0019others(23): Show | 29 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.511-327T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825697 | ||||||
chr8:11825821
|
C | T | 5 | a0001c0005t0001g0069a0001c0008t0001g0067a0001c0008t0001g0080others(2): Show | 5 | HG01891.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-203C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825821 | ||||||
chr8:11825836
|
A | G | 403 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(400): Show | 452 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(449): Show |
intron_variant | MODIFIER | c.511-188A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825836 | ||||||
chr8:11825882
|
G | C | 1 | a0001c0002t0003g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.511-142G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825882 | ||||||
chr8:11825893
|
T | A | 1 | a0001c0001t0002g0144 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.511-131T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825893 | ||||||
chr8:11825940
|
G | C | 6 | a0001c0003t0001g0187a0001c0003t0001g0264a0001c0003t0001g0273others(3): Show | 6 | NA18951.hp1 NA18979.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-84G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825940 | ||||||
chr8:11825987
|
T | G | 4 | a0001c0002t0003g0229a0001c0003t0003g0021a0001c0003t0003g0127others(1): Show | 5 | HG02071.hp2 NA18968.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-37T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825987 | ||||||
chr8:11826233
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+18T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826233 | ||||||
chr8:11826291
|
G | A | 2 | a0001c0001t0001g0317a0001c0002t0003g0029 | 3 | HG03654.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.702+76G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826291 | ||||||
chr8:11826309
|
T | C | 178 | a0001c0001t0001g0207a0001c0001t0001g0317a0001c0001t0002g0056others(175): Show | 197 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.702+94T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826309 | ||||||
chr8:11826355
|
C | A | 368 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(365): Show | 414 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(411): Show |
intron_variant | MODIFIER | c.702+140C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826355 | ||||||
chr8:11826355
|
C | T | 30 | a0001c0001t0001g0125a0001c0001t0002g0013a0001c0001t0002g0019others(27): Show | 33 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.702+140C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826355 | ||||||
chr8:11826365
|
G | T | 5 | a0001c0005t0001g0069a0001c0008t0001g0067a0001c0008t0001g0080others(2): Show | 5 | HG01891.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+150G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826365 | ||||||
chr8:11826538
|
G | A | 1 | a0001c0002t0003g0253 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.702+323G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826538 | ||||||
chr8:11826562
|
C | A | 175 | a0001c0001t0001g0207a0001c0001t0001g0317a0001c0001t0002g0056others(172): Show | 192 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.702+347C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826562 | ||||||
chr8:11826563
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+348C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826563 | ||||||
chr8:11826604
|
A | G | 1 | a0001c0004t0002g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.702+389A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826604 | ||||||
chr8:11826612
|
G | C | 2 | a0001c0002t0003g0197a0001c0003t0004g0386 | 2 | NA18940.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.702+397G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826612 | ||||||
chr8:11826632
|
C | A | 400 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(397): Show | 449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.702+417C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826632 | ||||||
chr8:11826756
|
G | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.702+541G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826756 | ||||||
chr8:11826757
|
G | C | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.702+542G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826757 | ||||||
chr8:11826779
|
C | T | 7 | a0001c0005t0001g0069a0001c0005t0012g0039a0001c0005t0012g0048others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+564C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826779 | ||||||
chr8:11826884
|
C | G | 1 | a0001c0002t0003g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702+669C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826884 | ||||||
chr8:11826888
|
G | C | 1 | a0001c0003t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.702+673G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826888 | ||||||
chr8:11826894
|
G | A | 171 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(168): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.702+679G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826894 | ||||||
chr8:11826950
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.702+735C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826950 | ||||||
chr8:11826954
|
A | G | 175 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(172): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.702+739A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826954 | ||||||
chr8:11827031
|
A | G | 2 | a0001c0001t0002g0126a0001c0003t0002g0164 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.702+816A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827031 | ||||||
chr8:11827115
|
T | A | 3 | a0001c0001t0001g0099a0001c0001t0011g0044a0001c0001t0011g0045 | 3 | HG02109.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.702+900T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827115 | ||||||
chr8:11827168
|
C | T | 2 | a0001c0005t0012g0039a0001c0005t0012g0048 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.702+953C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827168 | ||||||
chr8:11827212
|
A | G | 19 | a0001c0001t0002g0144a0001c0004t0002g0001a0001c0004t0002g0006others(16): Show | 30 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.702+997A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827212 | ||||||
chr8:11827278
|
T | G | 27 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(24): Show | 39 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.702+1063T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827278 | ||||||
chr8:11827292
|
T | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.702+1077T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827292 | ||||||
chr8:11827397
|
A | G | 2 | a0001c0004t0002g0178a0001c0011t0002g0014 | 3 | HG01891.hp2 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.702+1182A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827397 | ||||||
chr8:11827413
|
G | C | 3 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0001t0002g0388 | 3 | HG00733.hp2 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.702+1198G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827413 | ||||||
chr8:11827428
|
G | C | 2 | a0001c0001t0001g0319a0001c0001t0001g0376 | 2 | HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.702+1213G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827428 | ||||||
chr8:11827440
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.702+1225C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827440 | ||||||
chr8:11827441
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.702+1226G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827441 | ||||||
chr8:11827447
|
G | T | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1232G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827447 | ||||||
chr8:11827449
|
T | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1234T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827449 | ||||||
chr8:11827458
|
G | A | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1243G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827458 | ||||||
chr8:11827459
|
A | G | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1244A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827459 | ||||||
chr8:11827461
|
T | G | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1246T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827461 | ||||||
chr8:11827462
|
G | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1247G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827462 | ||||||
chr8:11827465
|
T | G | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1250T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827465 | ||||||
chr8:11827477
|
C | A | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.702+1262C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827477 | ||||||
chr8:11827501
|
G | C | 180 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0295others(177): Show | 199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.702+1286G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827501 | ||||||
chr8:11827575
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.702+1360G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827575 | ||||||
chr8:11827589
|
T | C | 1 | a0001c0003t0003g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.702+1374T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827589 | ||||||
chr8:11827606
|
A | G | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.702+1391A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827606 | ||||||
chr8:11827658
|
G | A | 1 | a0001c0004t0001g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.702+1443G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827658 | ||||||
chr8:11827667
|
A | T | 397 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(394): Show | 446 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(443): Show |
intron_variant | MODIFIER | c.702+1452A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827667 | ||||||
chr8:11827669
|
T | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1454T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827669 | ||||||
chr8:11827676
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.702+1461G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827676 | ||||||
chr8:11827688
|
A | G | 7 | a0001c0005t0001g0069a0001c0005t0012g0039a0001c0005t0012g0048others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+1473A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827688 | ||||||
chr8:11827811
|
T | C | 400 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(397): Show | 449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.702+1596T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827811 | ||||||
chr8:11827833
|
A | G | 264 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0125others(261): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.702+1618A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827833 | ||||||
chr8:11827837
|
C | T | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+1622C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827837 | ||||||
chr8:11827871
|
C | G | 4 | a0001c0003t0002g0404a0001c0003t0013g0405a0001c0015t0002g0181others(1): Show | 4 | HG02886.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+1656C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827871 | ||||||
chr8:11827875
|
TAAAAC | T | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(2): Show | 5 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+1685_702+1689d others(7): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827875 | |||||
chr8:11827875
|
TAAAACAA others(3): Show |
T | 1 | a0002c0009t0001g0174 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.702+1680_702+1689d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827875 | |||||
chr8:11827895
|
C | CA | 5 | a0001c0001t0001g0037a0001c0004t0006g0076a0002c0007t0001g0034others(2): Show | 6 | HG00323.hp1 HG01081.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+1684dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827895 | |||||
chr8:11827899
|
A | C | 1 | a0001c0001t0001g0339 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.702+1684A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827899 | ||||||
chr8:11827900
|
C | A | 198 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(195): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.702+1685C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827900 | ||||||
chr8:11827900
|
C | CA | 15 | a0001c0005t0001g0069a0001c0005t0002g0022a0001c0005t0002g0093others(12): Show | 16 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.702+1693dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827900 | |||||
chr8:11827928
|
A | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0331 | 2 | NA18941.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.702+1713A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827928 | ||||||
chr8:11827944
|
A | G | 27 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0050others(24): Show | 30 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.702+1729A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827944 | ||||||
chr8:11827996
|
G | A | 8 | a0001c0001t0006g0380a0001c0004t0006g0072a0001c0004t0006g0074others(5): Show | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+1781G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827996 | ||||||
chr8:11828027
|
C | T | 180 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0295others(177): Show | 199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.702+1812C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828027 | ||||||
chr8:11828035
|
C | T | 1 | a0001c0004t0001g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+1820C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828035 | ||||||
chr8:11828040
|
A | G | 7 | a0001c0005t0001g0069a0001c0005t0012g0039a0001c0005t0012g0048others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+1825A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828040 | ||||||
chr8:11828066
|
G | A | 1 | a0001c0006t0002g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.702+1851G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828066 | ||||||
chr8:11828074
|
C | T | 8 | a0001c0001t0006g0380a0001c0004t0006g0072a0001c0004t0006g0074others(5): Show | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+1859C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828074 | ||||||
chr8:11828082
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.702+1867G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828082 | ||||||
chr8:11828101
|
C | G | 2 | a0001c0001t0002g0126a0001c0003t0002g0164 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.702+1886C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828101 | ||||||
chr8:11828152
|
G | A | 1 | a0001c0002t0003g0246 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.702+1937G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828152 | ||||||
chr8:11828155
|
G | A | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.702+1940G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828155 | ||||||
chr8:11828163
|
C | T | 1 | a0001c0008t0001g0067 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.702+1948C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828163 | ||||||
chr8:11828171
|
C | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+1956C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828171 | ||||||
chr8:11828235
|
C | T | 179 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0295others(176): Show | 198 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.703-2009C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828235 | ||||||
chr8:11828243
|
G | A | 400 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(397): Show | 449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.703-2001G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828243 | ||||||
chr8:11828256
|
C | G | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-1988C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828256 | ||||||
chr8:11828264
|
C | T | 8 | a0001c0001t0006g0380a0001c0004t0006g0072a0001c0004t0006g0074others(5): Show | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.703-1980C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828264 | ||||||
chr8:11828292
|
AAAAC | A | 27 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0050others(24): Show | 30 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.703-1941_703-1938d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11828292 | |||||
chr8:11828300
|
C | G | 180 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0295others(177): Show | 199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.703-1944C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828300 | ||||||
chr8:11828310
|
C | A | 3 | a0001c0001t0004g0337a0001c0002t0003g0267a0001c0002t0003g0268 | 3 | HG01952.hp2 HG01975.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.703-1934C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828310 | ||||||
chr8:11828416
|
T | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1828T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828416 | ||||||
chr8:11828463
|
A | T | 1 | a0001c0001t0002g0090 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.703-1781A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828463 | ||||||
chr8:11828466
|
G | C | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.703-1778G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828466 | ||||||
chr8:11828472
|
C | G | 230 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0295others(227): Show | 266 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.703-1772C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828472 | ||||||
chr8:11828550
|
A | G | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703-1694A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828550 | ||||||
chr8:11828580
|
T | C | 45 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(42): Show | 60 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.703-1664T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828580 | ||||||
chr8:11828677
|
G | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1567G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828677 | ||||||
chr8:11828695
|
T | C | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703-1549T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828695 | ||||||
chr8:11828797
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.703-1447G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828797 | ||||||
chr8:11828904
|
C | T | 1 | a0001c0014t0016g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.703-1340C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828904 | ||||||
chr8:11828910
|
A | G | 255 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(252): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.703-1334A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828910 | ||||||
chr8:11828911
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1333A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828911 | ||||||
chr8:11828944
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1300A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828944 | ||||||
chr8:11828957
|
C | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-1287C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828957 | ||||||
chr8:11828958
|
T | A | 1 | a0001c0001t0001g0339 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.703-1286T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828958 | ||||||
chr8:11828978
|
T | G | 400 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(397): Show | 449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.703-1266T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828978 | ||||||
chr8:11829000
|
C | G | 2 | a0001c0005t0012g0039a0001c0005t0012g0048 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.703-1244C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829000 | ||||||
chr8:11829061
|
G | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-1183G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829061 | ||||||
chr8:11829071
|
G | C | 1 | a0001c0028t0002g0373 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.703-1173G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829071 | ||||||
chr8:11829146
|
CTTG | C | 136 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(133): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.703-1092_703-1090d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829146 | |||||
chr8:11829175
|
A | T | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703-1069A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829175 | ||||||
chr8:11829193
|
A | G | 1 | a0001c0002t0003g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.703-1051A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829193 | ||||||
chr8:11829199
|
A | C | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.703-1045A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829199 | ||||||
chr8:11829248
|
A | G | 3 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0001t0002g0388 | 3 | HG00733.hp2 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.703-996A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829248 | ||||||
chr8:11829261
|
A | G | 20 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0010g0042others(17): Show | 21 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.703-983A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829261 | ||||||
chr8:11829326
|
G | C | 129 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(126): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.703-918G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829326 | ||||||
chr8:11829396
|
T | G | 2 | a0001c0015t0002g0181a0001c0017t0002g0040 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.703-848T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829396 | ||||||
chr8:11829403
|
C | G | 26 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(23): Show | 38 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.703-841C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829403 | ||||||
chr8:11829482
|
T | A | 402 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(399): Show | 451 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(448): Show |
intron_variant | MODIFIER | c.703-762T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829482 | ||||||
chr8:11829525
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.703-719G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829525 | ||||||
chr8:11829545
|
T | G | 17 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0005t0001g0069others(14): Show | 18 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.703-699T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829545 | ||||||
chr8:11829546
|
T | A | 17 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0005t0001g0069others(14): Show | 18 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.703-698T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829546 | ||||||
chr8:11829549
|
C | G | 2 | a0001c0001t0008g0043a0001c0001t0008g0047 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.703-695C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829549 | ||||||
chr8:11829551
|
G | A | 2 | a0001c0005t0012g0039a0001c0005t0012g0048 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.703-693G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829551 | ||||||
chr8:11829553
|
T | C | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703-691T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829553 | ||||||
chr8:11829577
|
G | A | 7 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(4): Show | 7 | NA18941.hp1 NA18956.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-667G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829577 | ||||||
chr8:11829614
|
C | T | 7 | a0001c0004t0006g0072a0001c0004t0006g0074a0001c0004t0006g0075others(4): Show | 7 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-630C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829614 | ||||||
chr8:11829622
|
C | CT | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-621dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829622 | |||||
chr8:11829650
|
G | A | 107 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(104): Show | 118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.703-594G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829650 | ||||||
chr8:11829796
|
T | A | 1 | a0001c0002t0003g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.703-448T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829796 | ||||||
chr8:11829799
|
G | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-445G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829799 | ||||||
chr8:11829831
|
A | T | 2 | a0001c0002t0003g0204a0001c0002t0003g0248 | 2 | HG01358.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.703-413A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829831 | ||||||
chr8:11829834
|
G | GT | 50 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(47): Show | 65 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.703-401dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829834 | |||||
chr8:11829844
|
G | T | 14 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(11): Show | 16 | HG02258.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-400G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829844 | ||||||
chr8:11829845
|
T | G | 2 | a0001c0015t0002g0181a0001c0017t0002g0040 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.703-399T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829845 | ||||||
chr8:11829884
|
T | TTTTTTTT others(40): Show |
2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.703-359_703-358ins others(47): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829884 | |||||
chr8:11829884
|
T | TTTTTTTT others(42): Show |
1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.703-359_703-358ins others(49): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829884 | |||||
chr8:11829884
|
T | TTTTTTTT others(59): Show |
1 | a0001c0001t0002g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.703-359_703-358ins others(66): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829884 | |||||
chr8:11829887
|
A | G | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-357A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829887 | ||||||
chr8:11829935
|
C | T | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.703-309C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829935 | ||||||
chr8:11830002
|
C | T | 1 | a0001c0001t0008g0043 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703-242C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830002 | ||||||
chr8:11830009
|
G | A | 175 | a0001c0001t0001g0295a0001c0001t0002g0056a0001c0001t0002g0057others(172): Show | 192 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.703-235G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830009 | ||||||
chr8:11830050
|
C | A | 1 | a0001c0002t0003g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703-194C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830050 | ||||||
chr8:11830149
|
A | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-95A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830149 | ||||||
chr8:11830155
|
G | T | 2 | a0001c0002t0003g0239a0001c0002t0003g0253 | 2 | HG02129.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.703-89G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830155 | ||||||
chr8:11830174
|
C | T | 7 | a0001c0005t0001g0069a0001c0005t0012g0039a0001c0005t0012g0048others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-70C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830174 | ||||||
chr8:11830190
|
A | T | 1 | a0001c0003t0001g0375 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.703-54A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830190 | ||||||
chr8:11830235
|
T | C | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703-9T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830235 | ||||||
chr8:11830429
|
G | C | 401 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(398): Show | 450 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(447): Show |
intron_variant | MODIFIER | c.879+9G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830429 | ||||||
chr8:11830434
|
C | A | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+14C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830434 | ||||||
chr8:11830450
|
C | T | 170 | a0001c0001t0001g0295a0001c0001t0002g0056a0001c0001t0002g0057others(167): Show | 187 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.879+30C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830450 | ||||||
chr8:11830464
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.879+44G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830464 | ||||||
chr8:11830489
|
T | G | 8 | a0001c0001t0001g0033a0001c0001t0001g0301a0001c0001t0001g0302others(5): Show | 9 | HG01074.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+69T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830489 | ||||||
chr8:11830546
|
C | G | 15 | a0001c0001t0001g0295a0001c0002t0003g0051a0001c0002t0003g0052others(12): Show | 15 | HG01928.hp2 HG01943.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.879+126C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830546 | ||||||
chr8:11830564
|
A | T | 1 | a0001c0008t0001g0067 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.879+144A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830564 | ||||||
chr8:11830567
|
C | T | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.879+147C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830567 | ||||||
chr8:11830628
|
A | T | 7 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0005t0002g0093others(4): Show | 7 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+208A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830628 | ||||||
chr8:11830639
|
T | C | 316 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(313): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.879+219T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830639 | ||||||
chr8:11830654
|
C | A | 1 | a0002c0009t0002g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.879+234C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830654 | ||||||
chr8:11830795
|
G | A | 30 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(27): Show | 44 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.879+375G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830795 | ||||||
chr8:11830826
|
C | T | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+406C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830826 | ||||||
chr8:11830833
|
G | T | 30 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(27): Show | 44 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.879+413G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830833 | ||||||
chr8:11830884
|
T | C | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+464T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830884 | ||||||
chr8:11830953
|
G | A | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.879+533G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830953 | ||||||
chr8:11830976
|
A | C | 192 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(189): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.880-542A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830976 | ||||||
chr8:11831004
|
C | G | 1 | a0001c0001t0001g0403 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.880-514C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831004 | ||||||
chr8:11831098
|
G | A | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-420G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831098 | ||||||
chr8:11831110
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 7 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-408A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831110 | ||||||
chr8:11831167
|
C | G | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-351C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831167 | ||||||
chr8:11831251
|
T | G | 5 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(2): Show | 7 | HG02717.hp1 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-267T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831251 | ||||||
chr8:11831303
|
C | G | 1 | a0001c0001t0002g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.880-215C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831303 | ||||||
chr8:11831322
|
G | A | 8 | a0001c0002t0003g0226a0001c0002t0003g0252a0001c0002t0003g0277others(5): Show | 8 | HG00423.hp2 HG02132.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-196G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831322 | ||||||
chr8:11831378
|
A | G | 2 | a0001c0003t0001g0106a0001c0003t0001g0107 | 2 | NA18942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.880-140A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831378 | ||||||
chr8:11831451
|
C | T | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.880-67C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831451 | ||||||
chr8:11831499
|
CTCT | C | 49 | a0001c0002t0001g0031a0001c0002t0001g0055a0001c0002t0001g0060others(46): Show | 55 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.880-14_880-12delCT others(1): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 11831499 | |||||
chr8:11831712
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1032+42T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11831712 | ||||||
chr8:11831719
|
T | G | 320 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(317): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1032+49T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11831719 | ||||||
chr8:11831882
|
G | C | 1 | a0001c0003t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1032+212G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11831882 | ||||||
chr8:11832100
|
A | G | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1032+430A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832100 | ||||||
chr8:11832237
|
C | T | 14 | a0001c0001t0001g0020a0001c0001t0001g0147a0001c0001t0001g0148others(11): Show | 15 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1032+567C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832237 | ||||||
chr8:11832249
|
A | G | 38 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(35): Show | 52 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1032+579A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832249 | ||||||
chr8:11832250
|
CTAGGTT | C | 38 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(35): Show | 52 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1032+581_1032+586d others(8): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832250 | ||||||
chr8:11832254
|
G | A | 114 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(111): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1032+584G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832254 | ||||||
chr8:11832282
|
C | T | 1 | a0001c0004t0002g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1032+612C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832282 | ||||||
chr8:11832363
|
C | T | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00544.hp2 HG00597.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1032+693C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832363 | ||||||
chr8:11832367
|
C | T | 3 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0006t0001g0216 | 3 | NA18953.hp1 NA18957.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1032+697C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832367 | ||||||
chr8:11832442
|
C | G | 1 | a0001c0003t0001g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1032+772C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832442 | ||||||
chr8:11832516
|
C | T | 26 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(23): Show | 38 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1032+846C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832516 | ||||||
chr8:11832535
|
G | C | 2 | a0001c0002t0003g0184a0001c0002t0015g0223 | 2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1032+865G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832535 | ||||||
chr8:11832551
|
C | CAAAA | 8 | a0001c0003t0001g0049a0001c0003t0001g0103a0001c0003t0001g0116others(5): Show | 8 | HG01891.hp1 HG02074.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+903_1032+906d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA | 11 | a0001c0001t0001g0036a0001c0001t0002g0056a0001c0001t0002g0057others(8): Show | 12 | HG01358.hp2 HG01515.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1032+900_1032+906d others(9): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(1): Show |
35 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0001t0002g0126others(32): Show | 37 | HG00558.hp1 HG00621.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1032+899_1032+906d others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(2): Show |
31 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(28): Show | 34 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1032+898_1032+906d others(11): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(3): Show |
10 | a0001c0001t0002g0019a0001c0001t0002g0085a0001c0001t0002g0137others(7): Show | 11 | HG00323.hp2 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1032+897_1032+906d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0377a0001c0002t0001g0062 | 2 | HG00140.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1032+896_1032+906d others(13): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0083 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1032+895_1032+906d others(14): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0002g0086a0001c0001t0002g0095a0001c0001t0002g0096others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+894_1032+906d others(15): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0001g0292a0001c0001t0001g0317a0001c0001t0001g0364others(3): Show | 7 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032+893_1032+906d others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(8): Show |
30 | a0001c0001t0001g0012a0001c0001t0001g0302a0001c0001t0001g0312others(27): Show | 32 | HG00544.hp2 HG00621.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1032+892_1032+906d others(17): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(9): Show |
34 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0035others(31): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1032+891_1032+906d others(18): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(10): Show |
15 | a0001c0001t0001g0212a0001c0001t0001g0283a0001c0001t0001g0300others(12): Show | 15 | HG01243.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1032+890_1032+906d others(19): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(11): Show |
6 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0357others(3): Show | 6 | HG01515.hp2 HG01517.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032+889_1032+906d others(20): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0001g0359others(2): Show | 7 | HG00438.hp1 HG00544.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+888_1032+906d others(21): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0291a0001c0001t0001g0338a0001c0004t0001g0078others(1): Show | 4 | HG00597.hp2 HG02258.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+887_1032+906d others(22): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0322 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1032+886_1032+906d others(23): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0207a0001c0001t0001g0301a0001c0001t0001g0307others(2): Show | 5 | HG01978.hp1 HG02630.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+885_1032+906d others(24): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0003g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1032+883_1032+906d others(26): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0339 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1032+882_1032+906d others(27): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
CAA | C | 7 | a0001c0001t0002g0154a0001c0002t0003g0210a0001c0002t0003g0229others(4): Show | 7 | HG02572.hp1 NA18940.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+905_1032+906d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
CAAA | C | 121 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(118): Show | 137 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1032+904_1032+906d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
CAAAA | C | 7 | a0001c0001t0008g0046a0001c0002t0003g0198a0001c0002t0003g0243others(4): Show | 7 | HG01943.hp1 NA18906.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+903_1032+906d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832551
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0012t0001g0330 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1032+897_1032+906d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | |||||
chr8:11832576
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0362 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1032+906_1032+907i others(19): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832576 | ||||||
chr8:11832576
|
A | AT | 4 | a0001c0001t0002g0088a0001c0001t0006g0380a0001c0004t0002g0091others(1): Show | 4 | HG01255.hp1 HG02738.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+906_1032+907i others(3): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832576 | ||||||
chr8:11832576
|
A | T | 30 | a0001c0001t0002g0087a0001c0001t0002g0089a0001c0001t0002g0090others(27): Show | 42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1032+906A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832576 | ||||||
chr8:11832577
|
G | T | 38 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(35): Show | 52 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1032+907G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832577 | ||||||
chr8:11832579
|
C | G | 2 | a0001c0013t0002g0180a0011c0023t0017g0041 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1032+909C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832579 | ||||||
chr8:11832583
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1032+913G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832583 | ||||||
chr8:11832587
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1032+917C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832587 | ||||||
chr8:11832597
|
T | C | 322 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(319): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1032+927T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832597 | ||||||
chr8:11832617
|
T | C | 3 | a0001c0014t0016g0073a0001c0015t0002g0181a0001c0017t0002g0040 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1032+947T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832617 | ||||||
chr8:11832621
|
C | T | 3 | a0001c0014t0016g0073a0001c0015t0002g0181a0001c0017t0002g0040 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1032+951C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832621 | ||||||
chr8:11832661
|
C | T | 61 | a0001c0001t0002g0126a0001c0002t0001g0031a0001c0002t0001g0055others(58): Show | 67 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1032+991C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832661 | ||||||
chr8:11832668
|
C | A | 1 | a0001c0003t0001g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1032+998C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832668 | ||||||
chr8:11832668
|
C | G | 1 | a0001c0001t0003g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1032+998C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832668 | ||||||
chr8:11832671
|
A | T | 2 | a0001c0001t0008g0043a0001c0001t0008g0047 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1032+1001A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832671 | ||||||
chr8:11832724
|
C | T | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1032+1054C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832724 | ||||||
chr8:11832725
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0084a0001c0001t0002g0367others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1032+1055G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832725 | ||||||
chr8:11832786
|
C | A | 1 | a0001c0001t0001g0342 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1032+1116C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832786 | ||||||
chr8:11832862
|
T | C | 2 | a0001c0002t0001g0222a0001c0002t0001g0238 | 2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1032+1192T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832862 | ||||||
chr8:11832883
|
C | G | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1032+1213C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832883 | ||||||
chr8:11832894
|
G | A | 38 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(35): Show | 52 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1032+1224G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832894 | ||||||
chr8:11832907
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1032+1237C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832907 | ||||||
chr8:11832913
|
G | A | 150 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(147): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1032+1243G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832913 | ||||||
chr8:11832919
|
C | G | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1032+1249C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832919 | ||||||
chr8:11832955
|
C | A | 1 | a0001c0002t0003g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1032+1285C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832955 | ||||||
chr8:11833007
|
A | T | 1 | a0001c0002t0001g0269 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1032+1337A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833007 | ||||||
chr8:11833010
|
C | G | 5 | a0001c0001t0008g0043a0001c0001t0008g0046a0001c0001t0008g0047others(2): Show | 5 | HG02451.hp1 HG02647.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+1340C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833010 | ||||||
chr8:11833010
|
C | T | 1 | a0001c0004t0006g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1032+1340C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833010 | ||||||
chr8:11833013
|
C | A | 1 | a0001c0002t0004g0097 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1032+1343C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833013 | ||||||
chr8:11833025
|
C | T | 8 | a0001c0001t0006g0380a0001c0004t0006g0072a0001c0004t0006g0074others(5): Show | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+1355C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833025 | ||||||
chr8:11833048
|
A | T | 1 | a0001c0001t0001g0394 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1032+1378A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833048 | ||||||
chr8:11833164
|
C | T | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1032+1494C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833164 | ||||||
chr8:11833165
|
C | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0143 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1032+1495C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833165 | ||||||
chr8:11833291
|
C | A | 1 | a0001c0002t0003g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1032+1621C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833291 | ||||||
chr8:11833361
|
C | G | 8 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0005t0002g0093others(5): Show | 8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+1691C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833361 | ||||||
chr8:11833367
|
G | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1032+1697G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833367 | ||||||
chr8:11833406
|
A | G | 37 | a0001c0001t0001g0125a0001c0001t0002g0019a0001c0001t0002g0050others(34): Show | 41 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1032+1736A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833406 | ||||||
chr8:11833432
|
C | G | 2 | a0001c0004t0002g0063a0001c0004t0002g0064 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1032+1762C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833432 | ||||||
chr8:11833504
|
A | T | 9 | a0001c0001t0006g0380a0001c0004t0006g0072a0001c0004t0006g0074others(6): Show | 9 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1032+1834A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833504 | ||||||
chr8:11833517
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1032+1847T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833517 | ||||||
chr8:11833615
|
G | A | 1 | a0001c0004t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1032+1945G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833615 | ||||||
chr8:11833633
|
G | T | 117 | a0001c0001t0001g0020a0001c0001t0001g0125a0001c0001t0001g0147others(114): Show | 131 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1032+1963G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833633 | ||||||
chr8:11833636
|
G | A | 2 | a0001c0001t0002g0142a0001c0001t0002g0350 | 2 | HG01358.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1032+1966G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833636 | ||||||
chr8:11833694
|
C | G | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032+2024C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833694 | ||||||
chr8:11833696
|
T | A | 405 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(402): Show | 454 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(451): Show |
intron_variant | MODIFIER | c.1032+2026T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833696 | ||||||
chr8:11833801
|
T | G | 291 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(288): Show | 320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1032+2131T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833801 | ||||||
chr8:11833821
|
T | C | 397 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(394): Show | 446 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(443): Show |
intron_variant | MODIFIER | c.1032+2151T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833821 | ||||||
chr8:11833866
|
G | A | 1 | a0001c0014t0016g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1032+2196G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833866 | ||||||
chr8:11833884
|
C | T | 63 | a0001c0001t0002g0126a0001c0002t0001g0031a0001c0002t0001g0055others(60): Show | 69 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1032+2214C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833884 | ||||||
chr8:11834116
|
C | T | 7 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0005t0002g0155others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+2446C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834116 | ||||||
chr8:11834129
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1032+2459C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834129 | ||||||
chr8:11834165
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1032+2495T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834165 | ||||||
chr8:11834322
|
C | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1032+2652C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834322 | ||||||
chr8:11834430
|
T | G | 196 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(193): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1032+2760T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834430 | ||||||
chr8:11834489
|
C | T | 3 | a0001c0014t0016g0073a0001c0015t0002g0181a0001c0017t0002g0040 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1032+2819C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834489 | ||||||
chr8:11834589
|
C | CA | 63 | a0001c0001t0002g0126a0001c0002t0001g0031a0001c0002t0001g0055others(60): Show | 69 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1032+2922dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11834589 | |||||
chr8:11834594
|
G | C | 400 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(397): Show | 449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.1032+2924G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834594 | ||||||
chr8:11834598
|
C | G | 1 | a0001c0001t0001g0395 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1032+2928C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834598 | ||||||
chr8:11834619
|
T | C | 126 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(123): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1032+2949T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834619 | ||||||
chr8:11834831
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1032+3161T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834831 | ||||||
chr8:11834898
|
C | T | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1032+3228C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834898 | ||||||
chr8:11834952
|
T | A | 5 | a0001c0001t0002g0126a0001c0002t0002g0275a0001c0003t0002g0164others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+3282T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834952 | ||||||
chr8:11834972
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+3302C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834972 | ||||||
chr8:11835060
|
G | T | 180 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(177): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1033-3328G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835060 | ||||||
chr8:11835070
|
G | C | 5 | a0001c0005t0001g0069a0001c0008t0001g0067a0001c0008t0001g0080others(2): Show | 5 | HG01891.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033-3318G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835070 | ||||||
chr8:11835112
|
A | T | 1 | a0001c0002t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1033-3276A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835112 | ||||||
chr8:11835129
|
C | T | 33 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0050others(30): Show | 36 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1033-3259C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835129 | ||||||
chr8:11835157
|
C | T | 1 | a0001c0014t0016g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1033-3231C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835157 | ||||||
chr8:11835206
|
T | C | 7 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0118others(4): Show | 7 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-3182T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835206 | ||||||
chr8:11835314
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1033-3074C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835314 | ||||||
chr8:11835315
|
G | A | 5 | a0001c0001t0002g0126a0001c0002t0002g0275a0001c0003t0002g0164others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033-3073G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835315 | ||||||
chr8:11835322
|
C | G | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033-3066C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835322 | ||||||
chr8:11835332
|
C | T | 108 | a0001c0001t0003g0010a0001c0001t0003g0272a0001c0001t0004g0258others(105): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1033-3056C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835332 | ||||||
chr8:11835345
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1033-3043C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835345 | ||||||
chr8:11835362
|
A | G | 1 | a0001c0002t0003g0266 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1033-3026A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835362 | ||||||
chr8:11835371
|
C | T | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1033-3017C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835371 | ||||||
chr8:11835393
|
C | G | 1 | a0001c0001t0011g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1033-2995C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835393 | ||||||
chr8:11835413
|
C | T | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1033-2975C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835413 | ||||||
chr8:11835468
|
T | G | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1033-2920T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835468 | ||||||
chr8:11835472
|
G | A | 1 | a0001c0002t0003g0052 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1033-2916G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835472 | ||||||
chr8:11835539
|
A | G | 59 | a0001c0002t0001g0031a0001c0002t0001g0055a0001c0002t0001g0060others(56): Show | 65 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1033-2849A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835539 | ||||||
chr8:11835624
|
C | G | 1 | a0001c0003t0003g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1033-2764C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835624 | ||||||
chr8:11835670
|
C | A | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1033-2718C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835670 | ||||||
chr8:11835715
|
A | G | 7 | a0001c0005t0001g0069a0001c0005t0012g0039a0001c0005t0012g0048others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-2673A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835715 | ||||||
chr8:11835869
|
G | T | 348 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(345): Show | 394 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(391): Show |
intron_variant | MODIFIER | c.1033-2519G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835869 | ||||||
chr8:11835870
|
A | C | 9 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0005t0002g0022others(6): Show | 10 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1033-2518A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835870 | ||||||
chr8:11835877
|
T | C | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1033-2511T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835877 | ||||||
chr8:11835897
|
G | A | 25 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(22): Show | 37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1033-2491G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835897 | ||||||
chr8:11835930
|
G | T | 399 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(396): Show | 448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.1033-2458G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835930 | ||||||
chr8:11835932
|
G | A | 1 | a0001c0002t0003g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1033-2456G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835932 | ||||||
chr8:11835946
|
T | A | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1033-2442T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835946 | ||||||
chr8:11835948
|
A | C | 1 | a0001c0003t0001g0393 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1033-2440A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835948 | ||||||
chr8:11835971
|
T | TAAAA | 8 | a0001c0001t0001g0282a0001c0001t0001g0305a0001c0001t0001g0311others(5): Show | 8 | HG01257.hp1 HG01358.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-2396_1033-239 others(8): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAA | 128 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0033others(125): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1033-2397_1033-239 others(9): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAA | 127 | a0001c0001t0001g0011a0001c0001t0001g0099a0001c0001t0001g0147others(124): Show | 138 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1033-2398_1033-239 others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA | 31 | a0001c0001t0001g0212a0001c0001t0001g0316a0001c0001t0001g0326others(28): Show | 35 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1033-2399_1033-239 others(11): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(1): Show |
8 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(5): Show | 8 | HG01358.hp1 HG02071.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-2400_1033-239 others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(3): Show |
5 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0118others(2): Show | 5 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1033-2402_1033-239 others(14): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(4): Show |
3 | a0001c0001t0002g0059a0001c0001t0002g0163a0007c0020t0002g0058 | 3 | HG00639.hp2 HG02738.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1033-2403_1033-239 others(15): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(5): Show |
11 | a0001c0001t0002g0134a0001c0001t0002g0136a0001c0001t0002g0141others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1033-2404_1033-239 others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(6): Show |
6 | a0001c0001t0002g0019a0001c0001t0002g0132a0001c0001t0002g0133others(3): Show | 7 | HG00099.hp1 HG01106.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-2405_1033-239 others(17): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0002g0050 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1033-2406_1033-239 others(18): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(9): Show |
3 | a0001c0001t0002g0084a0001c0001t0002g0367a0001c0004t0002g0068 | 3 | HG02258.hp1 HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1033-2408_1033-239 others(20): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0002g0137 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1033-2409_1033-239 others(21): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0002g0013 | 3 | HG02922.hp1 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1033-2410_1033-239 others(22): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
TA | T | 8 | a0001c0001t0001g0306a0001c0001t0010g0042a0001c0004t0002g0015others(5): Show | 10 | HG02040.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1033-2393delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11835971
|
TAAAAAAA others(2): Show |
T | 35 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(32): Show | 48 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1033-2401_1033-239 others(13): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | |||||
chr8:11836039
|
C | G | 400 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(397): Show | 449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.1033-2349C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836039 | ||||||
chr8:11836068
|
G | A | 29 | a0001c0001t0002g0019a0001c0001t0002g0050a0001c0001t0002g0056others(26): Show | 30 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1033-2320G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836068 | ||||||
chr8:11836112
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1033-2276C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836112 | ||||||
chr8:11836121
|
C | G | 1 | a0001c0021t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1033-2267C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836121 | ||||||
chr8:11836139
|
C | A | 1 | a0001c0001t0002g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1033-2249C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836139 | ||||||
chr8:11836148
|
A | G | 2 | a0001c0001t0001g0151a0001c0004t0001g0079 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1033-2240A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836148 | ||||||
chr8:11836149
|
T | A | 1 | a0001c0002t0003g0253 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1033-2239T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836149 | ||||||
chr8:11836150
|
C | G | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1033-2238C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836150 | ||||||
chr8:11836152
|
T | TA | 217 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(214): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1033-2221dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836152 | |||||
chr8:11836152
|
T | TAA | 11 | a0001c0001t0001g0312a0001c0001t0002g0087a0001c0001t0002g0088others(8): Show | 11 | HG02738.hp1 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1033-2222_1033-222 others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836152 | |||||
chr8:11836152
|
T | TAAA | 40 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0050others(37): Show | 45 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1033-2223_1033-222 others(7): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836152 | |||||
chr8:11836171
|
A | G | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1033-2217A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836171 | ||||||
chr8:11836196
|
C | T | 2 | a0001c0003t0003g0021a0001c0003t0003g0127 | 3 | NA18968.hp1 NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1033-2192C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836196 | ||||||
chr8:11836234
|
ATTTTATG others(4): Show |
A | 2 | a0001c0001t0010g0042a0001c0004t0010g0179 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1033-2151_1033-214 others(15): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836234 | |||||
chr8:11836261
|
C | T | 3 | a0001c0001t0001g0151a0001c0004t0001g0079a0001c0005t0001g0150 | 3 | HG02559.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1033-2127C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836261 | ||||||
chr8:11836333
|
T | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1033-2055T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836333 | ||||||
chr8:11836410
|
T | C | 191 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(188): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1033-1978T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836410 | ||||||
chr8:11836437
|
C | T | 1 | a0001c0002t0015g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1033-1951C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836437 | ||||||
chr8:11836469
|
G | C | 1 | a0001c0028t0002g0373 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1033-1919G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836469 | ||||||
chr8:11836485
|
C | T | 5 | a0001c0001t0002g0126a0001c0002t0002g0275a0001c0003t0002g0164others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033-1903C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836485 | ||||||
chr8:11836587
|
C | T | 1 | a0001c0006t0005g0235 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1033-1801C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836587 | ||||||
chr8:11836790
|
C | G | 3 | a0001c0001t0001g0327a0001c0001t0001g0329a0001c0001t0001g0335 | 3 | HG00738.hp2 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1033-1598C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836790 | ||||||
chr8:11836855
|
G | A | 7 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0118others(4): Show | 7 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-1533G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836855 | ||||||
chr8:11836903
|
C | G | 1 | a0001c0003t0002g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1033-1485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836903 | ||||||
chr8:11836961
|
C | T | 1 | a0001c0002t0003g0255 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1033-1427C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836961 | ||||||
chr8:11837095
|
G | C | 113 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182others(110): Show | 128 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1033-1293G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837095 | ||||||
chr8:11837132
|
C | T | 8 | a0001c0001t0006g0380a0001c0004t0006g0072a0001c0004t0006g0074others(5): Show | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-1256C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837132 | ||||||
chr8:11837141
|
C | T | 13 | a0001c0001t0002g0019a0001c0001t0002g0133a0001c0001t0002g0134others(10): Show | 14 | HG00099.hp1 HG00738.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1033-1247C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837141 | ||||||
chr8:11837209
|
C | T | 3 | a0001c0014t0016g0073a0001c0015t0002g0181a0001c0017t0002g0040 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-1179C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837209 | ||||||
chr8:11837231
|
T | A | 10 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1033-1157T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837231 | ||||||
chr8:11837234
|
TTTTG | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1033-1146_1033-114 others(8): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11837234 | |||||
chr8:11837242
|
GT | G | 3 | a0001c0014t0016g0073a0001c0015t0002g0181a0001c0017t0002g0040 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-1140delT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11837242 | |||||
chr8:11837256
|
G | C | 32 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0050others(29): Show | 35 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1033-1132G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837256 | ||||||
chr8:11837358
|
T | A | 1 | a0001c0001t0001g0339 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1033-1030T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837358 | ||||||
chr8:11837382
|
C | T | 2 | a0001c0003t0002g0404a0001c0003t0013g0405 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1033-1006C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837382 | ||||||
chr8:11837411
|
T | C | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1033-977T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837411 | ||||||
chr8:11837455
|
C | T | 1 | a0001c0002t0003g0259 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1033-933C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837455 | ||||||
chr8:11837463
|
C | G | 7 | a0001c0005t0001g0069a0001c0005t0012g0039a0001c0005t0012g0048others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-925C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837463 | ||||||
chr8:11837477
|
G | A | 22 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0084others(19): Show | 25 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1033-911G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837477 | ||||||
chr8:11837490
|
C | T | 1 | a0008c0019t0001g0336 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1033-898C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837490 | ||||||
chr8:11837526
|
C | G | 2 | a0001c0001t0001g0396a0001c0001t0001g0397 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1033-862C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837526 | ||||||
chr8:11837551
|
G | A | 32 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0050others(29): Show | 35 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1033-837G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837551 | ||||||
chr8:11837622
|
C | T | 1 | a0002c0009t0002g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1033-766C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837622 | ||||||
chr8:11837652
|
T | C | 3 | a0001c0014t0016g0073a0001c0015t0002g0181a0001c0017t0002g0040 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-736T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837652 | ||||||
chr8:11837874
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1033-514G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837874 | ||||||
chr8:11837903
|
C | G | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0002g0063others(1): Show | 6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033-485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837903 | ||||||
chr8:11837925
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1033-463C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837925 | ||||||
chr8:11837994
|
G | A | 1 | a0002c0009t0002g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1033-394G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837994 | ||||||
chr8:11838046
|
G | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0182 | 3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1033-342G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838046 | ||||||
chr8:11838110
|
C | T | 1 | a0001c0001t0010g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1033-278C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838110 | ||||||
chr8:11838124
|
C | T | 1 | a0001c0001t0010g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1033-264C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838124 | ||||||
chr8:11838134
|
G | C | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1033-254G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838134 | ||||||
chr8:11838140
|
C | T | 1 | a0001c0004t0002g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1033-248C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838140 | ||||||
chr8:11838154
|
T | C | 2 | a0001c0004t0002g0063a0001c0004t0002g0064 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1033-234T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838154 | ||||||
chr8:11838191
|
C | G | 3 | a0001c0014t0016g0073a0001c0015t0002g0181a0001c0017t0002g0040 | 3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-197C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838191 | ||||||
chr8:11838222
|
C | G | 8 | a0001c0001t0006g0380a0001c0004t0006g0072a0001c0004t0006g0074others(5): Show | 8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-166C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838222 | ||||||
chr8:11838225
|
A | G | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1033-163A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838225 | ||||||
chr8:11838226
|
T | C | 7 | a0001c0002t0003g0184a0001c0002t0003g0203a0001c0002t0003g0219others(4): Show | 7 | HG00735.hp2 HG01070.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-162T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838226 | ||||||
chr8:11838363
|
T | C | 309 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(306): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1033-25T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838363 |