geneid | 2218 |
---|---|
ensemblid | ENSG00000106692.15 |
hgncid | 3622 |
symbol | FKTN |
name | fukutin |
refseq_nuc | NM_001079802.2 |
refseq_prot | NP_001073270.1 |
ensembl_nuc | ENST00000357998.10 |
ensembl_prot | ENSP00000350687.6 |
mane_status | MANE Select |
chr | chr9 |
start | 105558131 |
end | 105641118 |
strand | + |
ver | v1.2 |
region | chr9:105558131-105641118 |
region5000 | chr9:105553131-105646118 |
regionname0 | FKTN_chr9_105558131_105641118 |
regionname5000 | FKTN_chr9_105553131_105646118 |
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 | 1/0 | 461 | 302 | 57 | 41 | 167 | 8 | 28 | 135 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002 | 0/1 | 461 | 48 | 14 | 13 | 14 | 4 | 2 | 10 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0003 | 0/0 | 461 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0004 | 0/0 | 461 | 8 | 0 | 6 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0005 | 0/0 | 461 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0006 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0007 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0008 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0009 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
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 | 1/0 | 1386 | 291 | 49 | 41 | 164 | 8 | 28 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0002 | 0/1 | 1386 | 47 | 14 | 12 | 14 | 4 | 2 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0003 | 0/0 | 1386 | 13 | 13 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0004 | 0/0 | 1386 | 8 | 0 | 6 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0005 | 0/0 | 1386 | 5 | 5 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0006 | 0/0 | 1386 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0007 | 0/0 | 1386 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0008 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0010 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0011 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0012 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0013 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0014 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
c0015 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
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 | 1/0 | 6070 | 104 | 18 | 15 | 59 | 2 | 9 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0002 | 0/0 | 6070 | 83 | 10 | 12 | 55 | 3 | 3 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0003 | 0/0 | 6070 | 55 | 1 | 12 | 34 | 2 | 6 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0004 | 0/1 | 6070 | 30 | 10 | 11 | 3 | 3 | 2 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0005 | 0/0 | 6070 | 17 | 3 | 6 | 0 | 3 | 5 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0006 | 0/0 | 6069 | 16 | 14 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0007 | 0/0 | 6070 | 7 | 0 | 0 | 7 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0008 | 0/0 | 6070 | 5 | 0 | 1 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0009 | 0/0 | 6070 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0010 | 0/0 | 6070 | 4 | 4 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0011 | 0/0 | 6069 | 4 | 4 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0012 | 0/0 | 6070 | 4 | 3 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0013 | 0/0 | 6070 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0014 | 0/0 | 6069 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0015 | 0/0 | 6069 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0016 | 0/0 | 6070 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0017 | 0/0 | 6070 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0018 | 0/0 | 6069 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0019 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0020 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0021 | 0/0 | 6070 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0022 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0023 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0024 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0025 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0026 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0027 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0028 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0029 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0030 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0031 | 0/0 | 6106 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0032 | 0/0 | 6070 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0033 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0034 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0035 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0036 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0037 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0038 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0039 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0040 | 0/0 | 6070 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0041 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0042 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0043 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0044 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0045 | 0/0 | 6070 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0046 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0047 | 0/0 | 6069 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0048 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0049 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
t0050 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
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 | 4 | 0 | 2 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0007 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0033 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
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 | 1/0 | 1386 | 291 | 49 | 41 | 164 | 8 | 28 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0005 | 0/0 | 1386 | 5 | 5 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0006 | 0/0 | 1386 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0008 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0013 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0015 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002 | 0/1 | 1386 | 47 | 14 | 12 | 14 | 4 | 2 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0011 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0003c0003 | 0/0 | 1386 | 13 | 13 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0004c0004 | 0/0 | 1386 | 8 | 0 | 6 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0005c0007 | 0/0 | 1386 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0006c0010 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0007c0012 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0008c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0009c0014 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7455 | 84 | 7 | 14 | 51 | 2 | 9 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0002 | 0/0 | 7455 | 81 | 10 | 12 | 53 | 3 | 3 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0003 | 0/0 | 7455 | 54 | 1 | 12 | 33 | 2 | 6 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0005 | 0/0 | 7455 | 6 | 0 | 0 | 0 | 1 | 5 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0006 | 0/0 | 7454 | 16 | 14 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0007 | 0/0 | 7455 | 7 | 0 | 0 | 7 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0009 | 0/0 | 7455 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0010 | 0/0 | 7455 | 4 | 4 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0011 | 0/0 | 7454 | 4 | 4 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0012 | 0/0 | 7455 | 4 | 3 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0016 | 0/0 | 7455 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0017 | 0/0 | 7455 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0018 | 0/0 | 7454 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0027 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0029 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0030 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0031 | 0/0 | 7491 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0032 | 0/0 | 7455 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0033 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0034 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0035 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0036 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0037 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0038 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0039 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0040 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0042 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0044 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0045 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0046 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0047 | 0/0 | 7454 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0048 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0049 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0001t0050 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0005t0013 | 0/0 | 7455 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0005t0019 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0005t0026 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0006t0014 | 0/0 | 7454 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0006t0015 | 0/0 | 7454 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0008t0003 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0013t0002 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0001c0015t0002 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0001 | 0/0 | 7455 | 9 | 0 | 1 | 8 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0004 | 0/1 | 7455 | 27 | 9 | 10 | 2 | 3 | 2 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0008 | 0/0 | 7455 | 5 | 0 | 1 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0020 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0021 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0022 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0023 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0024 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0002t0025 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0002c0011t0004 | 0/0 | 7455 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0003c0003t0001 | 0/0 | 7455 | 11 | 11 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0003c0003t0004 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0003c0003t0028 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0004c0004t0005 | 0/0 | 7455 | 8 | 0 | 6 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0005c0007t0005 | 0/0 | 7455 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0006c0010t0041 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0007c0012t0004 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0008c0009t0015 | 0/0 | 7454 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
a0009c0014t0043 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | copy fasta | chr9 | 105553131 | 105646118 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0007 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0007g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0009g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0009g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0009g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0012g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0016g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0016g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0017g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0018g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0018g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0027g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0029g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0030g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0031g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0032g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0033g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0034g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0035g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0036g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0037g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0038g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0039g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0040g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0042g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0044g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0045g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0046g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0047g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0048g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0049g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0001t0050g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0005t0013g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0005t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0005t0019g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0005t0026g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0006t0014g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0006t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0006t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0008t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0013t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0001c0015t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0008g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0008g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0020g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0021g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0022g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0023g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0024g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0002t0025g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0002c0011t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0003c0003t0028g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0004c0004t0005g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0004c0004t0005g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0004c0004t0005g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0004c0004t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0004c0004t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0005c0007t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0005c0007t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0006c0010t0041g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0007c0012t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0008c0009t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
a0009c0014t0043g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00099 | hp2 | a0002 | c0002 | t0004 | g0029 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00140 | hp1 | a0004 | c0004 | t0005 | g0039 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0111 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0249 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0089 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00597 | hp1 | a0002 | c0002 | t0008 | g0202 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00609 | hp1 | a0001 | c0008 | t0003 | g0095 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00609 | hp2 | a0001 | c0001 | t0037 | g0164 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00639 | hp2 | a0002 | c0002 | t0004 | g0184 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00735 | hp1 | a0004 | c0004 | t0005 | g0253 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00735 | hp2 | a0002 | c0002 | t0004 | g0191 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG00741 | hp2 | a0002 | c0002 | t0004 | g0187 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01069 | hp1 | a0002 | c0002 | t0004 | g0192 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01074 | hp2 | a0002 | c0002 | t0004 | g0196 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01099 | hp2 | a0004 | c0004 | t0005 | g0038 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01167 | hp2 | a0004 | c0004 | t0005 | g0040 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01168 | hp1 | a0004 | c0004 | t0005 | g0039 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01192 | hp1 | a0002 | c0011 | t0004 | g0063 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01192 | hp2 | a0004 | c0004 | t0005 | g0038 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01243 | hp1 | a0002 | c0002 | t0004 | g0065 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0221 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01255 | hp2 | a0001 | c0001 | t0012 | g0059 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01257 | hp2 | a0002 | c0002 | t0004 | g0185 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01358 | hp2 | a0002 | c0002 | t0004 | g0186 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01361 | hp1 | a0002 | c0002 | t0004 | g0212 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01516 | hp1 | a0002 | c0002 | t0004 | g0030 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01516 | hp2 | a0002 | c0002 | t0021 | g0211 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01517 | hp1 | a0002 | c0002 | t0004 | g0030 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0079 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0054 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01884 | hp2 | a0002 | c0002 | t0004 | g0207 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01891 | hp2 | a0003 | c0003 | t0001 | g0233 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG01993 | hp2 | a0002 | c0002 | t0004 | g0064 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02004 | hp1 | a0002 | c0002 | t0008 | g0201 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02027 | hp1 | a0002 | c0002 | t0004 | g0183 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02055 | hp1 | a0002 | c0002 | t0004 | g0180 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02056 | hp2 | a0001 | c0001 | t0034 | g0115 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02071 | hp1 | a0001 | c0001 | t0048 | g0088 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02071 | hp2 | a0001 | c0001 | t0042 | g0261 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02080 | hp2 | a0001 | c0001 | t0017 | g0018 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02083 | hp1 | a0001 | c0001 | t0017 | g0018 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02148 | hp1 | a0001 | c0001 | t0032 | g0113 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02257 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02258 | hp1 | a0001 | c0005 | t0013 | g0032 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02258 | hp2 | a0001 | c0001 | t0018 | g0222 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02280 | hp2 | a0002 | c0002 | t0022 | g0203 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02300 | hp1 | a0004 | c0004 | t0005 | g0040 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02451 | hp1 | a0003 | c0003 | t0001 | g0228 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02451 | hp2 | a0001 | c0005 | t0026 | g0182 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0205 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02615 | hp2 | a0005 | c0007 | t0005 | g0035 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02622 | hp1 | a0002 | c0002 | t0020 | g0214 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0231 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02647 | hp2 | a0002 | c0002 | t0023 | g0204 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0229 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02723 | hp1 | a0001 | c0001 | t0027 | g0271 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02723 | hp2 | a0001 | c0006 | t0015 | g0051 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02738 | hp2 | a0002 | c0002 | t0004 | g0208 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02818 | hp1 | a0001 | c0001 | t0010 | g0055 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02886 | hp1 | a0003 | c0003 | t0001 | g0238 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02896 | hp1 | a0002 | c0002 | t0004 | g0197 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02896 | hp2 | a0001 | c0001 | t0029 | g0104 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02897 | hp1 | a0002 | c0002 | t0004 | g0198 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02965 | hp1 | a0005 | c0007 | t0005 | g0242 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0225 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02970 | hp2 | a0002 | c0002 | t0024 | g0199 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03041 | hp1 | a0001 | c0005 | t0013 | g0181 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0060 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03098 | hp2 | a0001 | c0001 | t0046 | g0057 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03130 | hp2 | a0006 | c0010 | t0041 | g0058 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0206 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03225 | hp2 | a0002 | c0002 | t0004 | g0031 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03486 | hp1 | a0001 | c0006 | t0014 | g0048 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03486 | hp2 | a0001 | c0005 | t0019 | g0190 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03492 | hp2 | a0002 | c0002 | t0004 | g0029 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03516 | hp1 | a0001 | c0006 | t0014 | g0049 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03516 | hp2 | a0002 | c0002 | t0004 | g0188 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03540 | hp1 | a0009 | c0014 | t0043 | g0067 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0230 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0241 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0195 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03669 | hp1 | a0001 | c0001 | t0045 | g0234 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03669 | hp2 | a0001 | c0001 | t0016 | g0156 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0248 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0251 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03831 | hp2 | a0001 | c0001 | t0040 | g0250 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG04228 | hp1 | a0001 | c0001 | t0016 | g0117 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0243 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18522 | hp2 | a0005 | c0007 | t0005 | g0035 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18945 | hp1 | a0001 | c0001 | t0039 | g0159 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18948 | hp1 | a0002 | c0002 | t0008 | g0008 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18951 | hp2 | a0002 | c0002 | t0008 | g0008 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18957 | hp1 | a0001 | c0001 | t0009 | g0309 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18959 | hp2 | a0001 | c0001 | t0009 | g0277 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18966 | hp2 | a0001 | c0001 | t0031 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18972 | hp2 | a0001 | c0001 | t0036 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18974 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18981 | hp1 | a0001 | c0001 | t0050 | g0005 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18983 | hp2 | a0001 | c0001 | t0033 | g0170 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18988 | hp1 | a0001 | c0015 | t0002 | g0023 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18988 | hp2 | a0002 | c0002 | t0008 | g0008 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18990 | hp1 | a0001 | c0001 | t0044 | g0011 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18999 | hp1 | a0001 | c0001 | t0030 | g0151 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19001 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19002 | hp2 | a0001 | c0001 | t0049 | g0099 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19007 | hp1 | a0001 | c0001 | t0009 | g0282 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19009 | hp1 | a0001 | c0001 | t0035 | g0126 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19030 | hp1 | a0001 | c0001 | t0047 | g0236 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0240 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19043 | hp1 | a0002 | c0002 | t0025 | g0200 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19057 | hp1 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19060 | hp2 | a0002 | c0002 | t0004 | g0193 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19067 | hp1 | a0007 | c0012 | t0004 | g0213 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19083 | hp2 | a0001 | c0013 | t0002 | g0311 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19090 | hp1 | a0001 | c0001 | t0009 | g0046 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19090 | hp2 | a0001 | c0001 | t0038 | g0160 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0312 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ASW | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20129 | hp2 | a0003 | c0003 | t0001 | g0227 | AFR | ASW | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | TSI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20752 | hp2 | a0004 | c0004 | t0005 | g0252 | EUR | TSI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | GIH | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0244 | SAS | GIH | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02109 | hp1 | a0001 | c0001 | t0018 | g0224 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02109 | hp2 | a0001 | c0005 | t0013 | g0032 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0209 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG02559 | hp2 | a0002 | c0002 | t0004 | g0031 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0061 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG03471 | hp2 | a0008 | c0009 | t0015 | g0050 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG06807 | hp1 | a0001 | c0001 | t0010 | g0053 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
HG06807 | hp2 | a0003 | c0003 | t0028 | g0232 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0210 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA21309 | hp1 | a0002 | c0002 | t0004 | g0189 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
NA21309 | hp2 | a0003 | c0003 | t0001 | g0239 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0004 | g0194 | REF | REF | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0275 | REF | REF | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105573742
|
CA | C | 1 | a0001 | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
splice_region_variant | LOW | c.-90delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 105573742 | |||||
chr9:105601145
|
C | T | 1 | a0004 | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.166C>T | p.Arg56Cys | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/11 | 381/7455 | 166/1386 | 56/461 | chr9 | 105601145 | ||
chr9:105601146
|
G | A | 1 | a0006 | 1 | HG03130.hp2 | missense_variant&splice_region_variant | MODERATE | c.167G>A | p.Arg56His | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/11 | 382/7455 | 167/1386 | 56/461 | chr9 | 105601146 | ||
chr9:105604218
|
G | A | 1 | a0003 | 13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
missense_variant | MODERATE | c.373G>A | p.Gly125Ser | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/11 | 588/7455 | 373/1386 | 125/461 | chr9 | 105604218 | ||
chr9:105604453
|
G | A | 2 | a0002a0007 | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
missense_variant | MODERATE | c.608G>A | p.Arg203Gln | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/11 | 823/7455 | 608/1386 | 203/461 | chr9 | 105604453 | ||
chr9:105607839
|
C | T | 1 | a0005 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.668C>T | p.Thr223Ile | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/11 | 883/7455 | 668/1386 | 223/461 | chr9 | 105607839 | ||
chr9:105607926
|
A | T | 1 | a0008 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.755A>T | p.Tyr252Phe | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/11 | 970/7455 | 755/1386 | 252/461 | chr9 | 105607926 | ||
chr9:105615351
|
C | T | 1 | a0007 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.854C>T | p.Ala285Val | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/11 | 1069/7455 | 854/1386 | 285/461 | chr9 | 105615351 | ||
chr9:105635214
|
A | G | 1 | a0009 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1336A>G | p.Asn446Asp | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1551/7455 | 1336/1386 | 446/461 | chr9 | 105635214 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105575062
|
G | A | 1 | a0001c0008 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.30G>A | p.Leu10Leu | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 245/7455 | 30/1386 | 10/461 | chr9 | 105575062 | ||
chr9:105575074
|
G | A | 2 | a0001c0006a0008c0009 | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.42G>A | p.Thr14Thr | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 257/7455 | 42/1386 | 14/461 | chr9 | 105575074 | ||
chr9:105575075
|
C | T | 1 | a0001c0015 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.43C>T | p.Leu15Leu | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 258/7455 | 43/1386 | 15/461 | chr9 | 105575075 | ||
chr9:105618074
|
C | A | 3 | a0001c0005a0002c0002a0007c0012 | 53 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
synonymous_variant | LOW | c.1026C>A | p.Leu342Leu | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/11 | 1241/7455 | 1026/1386 | 342/461 | chr9 | 105618074 | ||
chr9:105635108
|
T | C | 1 | a0001c0013 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1230T>C | p.His410His | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1445/7455 | 1230/1386 | 410/461 | chr9 | 105635108 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105558154
|
CT | C | 3 | a0001c0006t0014a0001c0006t0015a0008c0009t0015 | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-191delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/11 | 16878 | chr9 | 105558154 | |||||
chr9:105573677
|
G | C | 14 | a0001c0005t0013a0001c0005t0019a0001c0005t0026others(11): Show | 46 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-158G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | 1356 | chr9 | 105573677 | |||||
chr9:105573727
|
A | T | 1 | a0001c0001t0012 | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-108A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | 1306 | chr9 | 105573727 | |||||
chr9:105573739
|
T | C | 1 | a0001c0001t0027 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-96T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | 1294 | chr9 | 105573739 | |||||
chr9:105574988
|
G | T | 2 | a0001c0005t0013a0001c0005t0026 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-45G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 45 | chr9 | 105574988 | |||||
chr9:105635318
|
G | T | 1 | a0002c0002t0025 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 54 | chr9 | 105635318 | |||||
chr9:105635343
|
C | T | 1 | a0001c0001t0050 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 79 | chr9 | 105635343 | |||||
chr9:105635563
|
C | A | 1 | a0003c0003t0028 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 299 | chr9 | 105635563 | |||||
chr9:105635785
|
A | G | 1 | a0002c0002t0024 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*521A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 521 | chr9 | 105635785 | |||||
chr9:105636041
|
C | A | 1 | a0001c0001t0016 | 2 | HG03669.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*777C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 777 | chr9 | 105636041 | |||||
chr9:105636050
|
T | G | 16 | a0001c0001t0002a0001c0001t0007a0001c0001t0016others(13): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*786T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 786 | chr9 | 105636050 | |||||
chr9:105636070
|
G | C | 1 | a0001c0001t0011 | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*806G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 806 | chr9 | 105636070 | |||||
chr9:105636082
|
C | T | 1 | a0001c0005t0026 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 818 | chr9 | 105636082 | |||||
chr9:105636241
|
C | T | 1 | a0001c0001t0018 | 2 | HG02109.hp1 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*977C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 977 | chr9 | 105636241 | |||||
chr9:105636282
|
T | A | 1 | a0002c0002t0008 | 5 | HG00597.hp1 HG02004.hp1 NA18948.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1018T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1018 | chr9 | 105636282 | |||||
chr9:105636397
|
A | G | 8 | a0001c0001t0003a0001c0001t0017a0001c0001t0038others(5): Show | 62 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1133A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1133 | chr9 | 105636397 | |||||
chr9:105636493
|
A | G | 2 | a0002c0002t0022a0002c0002t0023 | 2 | HG02280.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1229A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1229 | chr9 | 105636493 | |||||
chr9:105636513
|
C | T | 1 | a0001c0001t0037 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1249C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1249 | chr9 | 105636513 | |||||
chr9:105636553
|
G | A | 1 | a0001c0001t0029 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1289 | chr9 | 105636553 | |||||
chr9:105636587
|
C | T | 3 | a0001c0006t0014a0001c0006t0015a0008c0009t0015 | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1323C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1323 | chr9 | 105636587 | |||||
chr9:105636902
|
A | G | 1 | a0001c0001t0047 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1638 | chr9 | 105636902 | |||||
chr9:105637107
|
A | T | 2 | a0001c0001t0007a0001c0001t0036 | 8 | NA18952.hp2 NA18961.hp2 NA18972.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1843A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1843 | chr9 | 105637107 | |||||
chr9:105637123
|
G | C | 1 | a0001c0001t0012 | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1859G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1859 | chr9 | 105637123 | |||||
chr9:105637162
|
A | G | 2 | a0001c0006t0015a0008c0009t0015 | 2 | HG02723.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1898A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1898 | chr9 | 105637162 | |||||
chr9:105637321
|
G | A | 1 | a0001c0001t0038 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2057G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2057 | chr9 | 105637321 | |||||
chr9:105637544
|
T | C | 9 | a0001c0001t0003a0001c0001t0017a0001c0001t0038others(6): Show | 63 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2280T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2280 | chr9 | 105637544 | |||||
chr9:105637562
|
C | G | 2 | a0001c0001t0010a0001c0001t0012 | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2298C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2298 | chr9 | 105637562 | |||||
chr9:105637691
|
G | T | 1 | a0002c0002t0024 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2427G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2427 | chr9 | 105637691 | |||||
chr9:105637856
|
T | C | 1 | a0006c0010t0041 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2592T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2592 | chr9 | 105637856 | |||||
chr9:105637904
|
G | A | 1 | a0001c0001t0048 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2640G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2640 | chr9 | 105637904 | |||||
chr9:105638052
|
C | T | 1 | a0002c0002t0021 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2788C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2788 | chr9 | 105638052 | |||||
chr9:105638149
|
G | A | 1 | a0002c0002t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2885G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2885 | chr9 | 105638149 | |||||
chr9:105638174
|
C | A | 2 | a0001c0001t0017a0001c0001t0048 | 3 | HG02071.hp1 HG02080.hp2 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2910C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2910 | chr9 | 105638174 | |||||
chr9:105638194
|
G | T | 1 | a0001c0001t0035 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2930G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2930 | chr9 | 105638194 | |||||
chr9:105638259
|
T | G | 3 | a0001c0006t0014a0001c0006t0015a0008c0009t0015 | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2995T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2995 | chr9 | 105638259 | |||||
chr9:105638360
|
G | C | 1 | a0001c0001t0036 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3096G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3096 | chr9 | 105638360 | |||||
chr9:105638390
|
C | G | 1 | a0001c0001t0046 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3126C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3126 | chr9 | 105638390 | |||||
chr9:105638616
|
C | A | 1 | a0001c0001t0030 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3352C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3352 | chr9 | 105638616 | |||||
chr9:105638629
|
G | A | 1 | a0001c0001t0042 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3365G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3365 | chr9 | 105638629 | |||||
chr9:105638641
|
A | G | 2 | a0001c0001t0009a0001c0001t0034 | 5 | HG02056.hp2 NA18957.hp1 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3377A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3377 | chr9 | 105638641 | |||||
chr9:105639042
|
T | C | 8 | a0001c0001t0010a0001c0001t0012a0001c0001t0046others(5): Show | 15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3778T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3778 | chr9 | 105639042 | |||||
chr9:105639130
|
C | T | 2 | a0001c0006t0015a0008c0009t0015 | 2 | HG02723.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3866C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3866 | chr9 | 105639130 | |||||
chr9:105639595
|
A | T | 1 | a0001c0001t0033 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4331A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4331 | chr9 | 105639595 | |||||
chr9:105639642
|
GA | G | 3 | a0001c0001t0006a0001c0001t0018a0001c0001t0047 | 19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4388delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4388 | INFO_REALIGN_3_PRIME | chr9 | 105639642 | ||||
chr9:105639755
|
T | C | 1 | a0009c0014t0043 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4491T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4491 | chr9 | 105639755 | |||||
chr9:105639765
|
A | G | 1 | a0001c0001t0033 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4501A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4501 | chr9 | 105639765 | |||||
chr9:105640089
|
T | C | 3 | a0001c0001t0010a0001c0001t0012a0001c0005t0019 | 9 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4825T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4825 | chr9 | 105640089 | |||||
chr9:105640305
|
G | A | 6 | a0001c0001t0005a0001c0001t0006a0001c0001t0018others(3): Show | 36 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5041G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5041 | chr9 | 105640305 | |||||
chr9:105640326
|
G | A | 3 | a0001c0001t0006a0001c0001t0018a0001c0001t0047 | 19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5062G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5062 | chr9 | 105640326 | |||||
chr9:105640348
|
C | T | 1 | a0002c0002t0020 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5084C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5084 | chr9 | 105640348 | |||||
chr9:105640349
|
G | A | 1 | a0001c0001t0044 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5085G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5085 | chr9 | 105640349 | |||||
chr9:105640376
|
C | A | 1 | a0001c0001t0049 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5112C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5112 | chr9 | 105640376 | |||||
chr9:105640516
|
G | A | 1 | a0001c0005t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5252G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5252 | chr9 | 105640516 | |||||
chr9:105640524
|
G | T | 6 | a0001c0001t0003a0001c0001t0017a0001c0001t0048others(3): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5260G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5260 | chr9 | 105640524 | |||||
chr9:105640559
|
A | G | 1 | a0001c0001t0046 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5295A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5295 | chr9 | 105640559 | |||||
chr9:105640781
|
T | C | 1 | a0001c0001t0010 | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5517T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5517 | chr9 | 105640781 | |||||
chr9:105640882
|
T | A | 17 | a0001c0001t0002a0001c0001t0007a0001c0001t0016others(14): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*5618T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5618 | chr9 | 105640882 | |||||
chr9:105640905
|
A | G | 1 | a0001c0001t0032 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5641A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5641 | chr9 | 105640905 | |||||
chr9:105640938
|
C | T | 1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5674C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5674 | chr9 | 105640938 | |||||
chr9:105640945
|
A | T | 1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5681A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5681 | chr9 | 105640945 | |||||
chr9:105640947
|
A | T | 1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5683A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5683 | chr9 | 105640947 | |||||
chr9:105640951
|
T | TTTCTGTT others(29): Show |
1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5687_*5688insTTCT others(32): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5688 | chr9 | 105640951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105558205
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+40T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558205 | ||||||
chr9:105558400
|
G | A | 1 | a0001c0001t0006g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-181+235G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558400 | ||||||
chr9:105558585
|
T | G | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-181+420T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558585 | ||||||
chr9:105558630
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+465G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558630 | ||||||
chr9:105558636
|
GA | G | 12 | a0001c0001t0001g0313a0001c0001t0006g0014a0001c0001t0006g0312others(9): Show | 14 | HG01255.hp2 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-181+485delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105558636 | |||||
chr9:105558650
|
A | C | 1 | a0001c0001t0001g0313 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-181+485A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558650 | ||||||
chr9:105558707
|
G | A | 198 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(195): Show | 228 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-181+542G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558707 | ||||||
chr9:105558793
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 5 | HG00099.hp1 HG00280.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-181+628G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558793 | ||||||
chr9:105558874
|
C | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+709C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558874 | ||||||
chr9:105559084
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+919A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559084 | ||||||
chr9:105559302
|
G | C | 1 | a0001c0001t0010g0053 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-181+1137G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559302 | ||||||
chr9:105559483
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1318A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559483 | ||||||
chr9:105559541
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1376G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559541 | ||||||
chr9:105559603
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1438G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559603 | ||||||
chr9:105559684
|
C | CA | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+1533dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105559684 | |||||
chr9:105559743
|
G | A | 2 | a0002c0002t0004g0064a0002c0002t0004g0065 | 2 | HG01243.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-181+1578G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559743 | ||||||
chr9:105559755
|
T | C | 1 | a0001c0001t0006g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-181+1590T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559755 | ||||||
chr9:105559836
|
G | C | 243 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0220others(240): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-181+1671G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559836 | ||||||
chr9:105560109
|
C | G | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+1944C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560109 | ||||||
chr9:105560254
|
C | T | 5 | a0004c0004t0005g0038a0004c0004t0005g0039a0004c0004t0005g0040others(2): Show | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-181+2089C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560254 | ||||||
chr9:105560274
|
T | G | 1 | a0001c0001t0002g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-181+2109T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560274 | ||||||
chr9:105560330
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-181+2165G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560330 | ||||||
chr9:105560518
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2353T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560518 | ||||||
chr9:105560522
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2357C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560522 | ||||||
chr9:105560809
|
C | G | 1 | a0001c0001t0003g0215 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-181+2644C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560809 | ||||||
chr9:105560828
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2663T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560828 | ||||||
chr9:105560845
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0220 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-181+2680T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560845 | ||||||
chr9:105560870
|
C | T | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-181+2705C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560870 | ||||||
chr9:105560920
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2755C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560920 | ||||||
chr9:105561046
|
A | G | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+2881A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561046 | ||||||
chr9:105561084
|
CAAAAAAC others(5): Show |
C | 1 | a0004c0004t0005g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-181+2931_-181+294 others(16): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561084 | |||||
chr9:105561091
|
CA | C | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+2937delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561091 | |||||
chr9:105561282
|
A | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+3117A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561282 | ||||||
chr9:105561327
|
TAC | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+3164_-181+316 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561327 | |||||
chr9:105561566
|
T | A | 1 | a0002c0002t0004g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3401T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561566 | ||||||
chr9:105561569
|
T | A | 1 | a0002c0002t0004g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3404T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561569 | ||||||
chr9:105561570
|
T | C | 1 | a0002c0002t0004g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3405T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561570 | ||||||
chr9:105561571
|
C | A | 1 | a0002c0002t0004g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3406C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561571 | ||||||
chr9:105561641
|
A | C | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+3476A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561641 | ||||||
chr9:105561783
|
A | G | 1 | a0002c0002t0020g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-181+3618A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561783 | ||||||
chr9:105561828
|
T | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+3663T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561828 | ||||||
chr9:105561925
|
A | AT | 9 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0002g0028others(6): Show | 10 | HG01258.hp1 HG02523.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+3775dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561925 | |||||
chr9:105561925
|
AT | A | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+3775delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561925 | |||||
chr9:105562004
|
ATCTC | A | 4 | a0001c0001t0006g0221a0001c0001t0006g0223a0001c0001t0018g0222others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+3843_-181+384 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105562004 | |||||
chr9:105562033
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+3868C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562033 | ||||||
chr9:105562149
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-181+3984C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562149 | ||||||
chr9:105562169
|
T | C | 65 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0255others(62): Show | 81 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-181+4004T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562169 | ||||||
chr9:105562399
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4234G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562399 | ||||||
chr9:105562543
|
G | C | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-181+4378G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562543 | ||||||
chr9:105562601
|
C | A | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-181+4436C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562601 | ||||||
chr9:105562619
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4454C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562619 | ||||||
chr9:105562624
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4459T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562624 | ||||||
chr9:105562649
|
G | A | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+4484G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562649 | ||||||
chr9:105562746
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4581C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562746 | ||||||
chr9:105562831
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4666T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562831 | ||||||
chr9:105562853
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0305a0001c0001t0001g0306 | 5 | HG01109.hp1 HG02615.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-181+4688A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562853 | ||||||
chr9:105562903
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4738C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562903 | ||||||
chr9:105562904
|
T | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4739T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562904 | ||||||
chr9:105562961
|
C | A | 1 | a0002c0002t0004g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-181+4796C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562961 | ||||||
chr9:105562999
|
A | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-181+4834A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562999 | ||||||
chr9:105563113
|
C | G | 1 | a0002c0002t0004g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-181+4948C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563113 | ||||||
chr9:105563172
|
G | T | 1 | a0001c0001t0003g0006 | 3 | NA18951.hp1 NA19056.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-181+5007G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563172 | ||||||
chr9:105563181
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-181+5016A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563181 | ||||||
chr9:105563199
|
C | T | 19 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0020others(16): Show | 24 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.-181+5034C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563199 | ||||||
chr9:105563201
|
C | A | 8 | a0002c0002t0004g0029a0002c0002t0004g0030a0002c0002t0004g0184others(5): Show | 10 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-181+5036C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563201 | ||||||
chr9:105563237
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5072C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563237 | ||||||
chr9:105563238
|
G | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5073G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563238 | ||||||
chr9:105563239
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-181+5074G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563239 | ||||||
chr9:105563302
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-181+5137G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563302 | ||||||
chr9:105563322
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5157C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563322 | ||||||
chr9:105563328
|
G | A | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-181+5163G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563328 | ||||||
chr9:105563332
|
G | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5167G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563332 | ||||||
chr9:105563382
|
CAG | C | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+5218_-181+521 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563382 | ||||||
chr9:105563418
|
C | G | 5 | a0004c0004t0005g0038a0004c0004t0005g0039a0004c0004t0005g0040others(2): Show | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-181+5253C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563418 | ||||||
chr9:105563446
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5281C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563446 | ||||||
chr9:105563508
|
C | A | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-181+5343C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563508 | ||||||
chr9:105563593
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0220a0001c0001t0012g0059others(3): Show | 7 | HG01081.hp2 HG01255.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+5428G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563593 | ||||||
chr9:105563598
|
T | TG | 26 | a0001c0001t0001g0041a0001c0001t0001g0303a0001c0001t0001g0304others(23): Show | 31 | HG00280.hp1 HG00741.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.-181+5444dupG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105563598 | |||||
chr9:105563598
|
TG | T | 154 | a0001c0001t0001g0107a0001c0001t0001g0258a0001c0001t0002g0003others(151): Show | 177 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.-181+5444delG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105563598 | |||||
chr9:105563601
|
G | T | 2 | a0002c0002t0004g0180a0002c0002t0021g0211 | 2 | HG01516.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-181+5436G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563601 | ||||||
chr9:105563602
|
G | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5437G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563602 | ||||||
chr9:105563603
|
G | GT | 5 | a0004c0004t0005g0038a0004c0004t0005g0039a0004c0004t0005g0040others(2): Show | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-181+5438_-181+543 others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563603 | ||||||
chr9:105563604
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0313 | 2 | NA18979.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-181+5439G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563604 | ||||||
chr9:105563605
|
G | C | 1 | a0001c0001t0007g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-181+5440G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563605 | ||||||
chr9:105563606
|
G | C | 1 | a0001c0001t0029g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-181+5441G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563606 | ||||||
chr9:105563614
|
C | T | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5449C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563614 | ||||||
chr9:105563644
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5479G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563644 | ||||||
chr9:105563714
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-181+5549T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563714 | ||||||
chr9:105563760
|
T | A | 1 | a0002c0002t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-181+5595T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563760 | ||||||
chr9:105563827
|
GA | G | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5663delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563827 | ||||||
chr9:105563853
|
C | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+5688C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563853 | ||||||
chr9:105563916
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5751T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563916 | ||||||
chr9:105563933
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-181+5768G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563933 | ||||||
chr9:105564051
|
A | C | 2 | a0005c0007t0005g0035a0005c0007t0005g0242 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+5886A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564051 | ||||||
chr9:105564051
|
A | T | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5886A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564051 | ||||||
chr9:105564078
|
A | G | 2 | a0002c0002t0004g0207a0002c0002t0020g0214 | 2 | HG01884.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-181+5913A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564078 | ||||||
chr9:105564298
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6133G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564298 | ||||||
chr9:105564307
|
C | T | 199 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(196): Show | 229 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-181+6142C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564307 | ||||||
chr9:105564327
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0220a0004c0004t0005g0253 | 4 | HG00735.hp1 HG01081.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+6162G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564327 | ||||||
chr9:105564335
|
C | T | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302 | 3 | HG01069.hp2 HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-181+6170C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564335 | ||||||
chr9:105564349
|
C | T | 3 | a0003c0003t0001g0238a0003c0003t0001g0239a0003c0003t0001g0240 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-181+6184C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564349 | ||||||
chr9:105564370
|
A | G | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-181+6205A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564370 | ||||||
chr9:105564436
|
T | C | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6271T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564436 | ||||||
chr9:105564496
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6331A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564496 | ||||||
chr9:105564508
|
C | G | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+6343C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564508 | ||||||
chr9:105564558
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6393A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564558 | ||||||
chr9:105564665
|
C | T | 1 | a0001c0001t0003g0019 | 2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-181+6500C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564665 | ||||||
chr9:105564666
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-181+6501G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564666 | ||||||
chr9:105564670
|
G | A | 3 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061 | 3 | HG01255.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-181+6505G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564670 | ||||||
chr9:105564686
|
A | T | 2 | a0001c0006t0015g0051a0008c0009t0015g0050 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-181+6521A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564686 | ||||||
chr9:105564736
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6571C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564736 | ||||||
chr9:105564915
|
A | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+6750A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564915 | ||||||
chr9:105565045
|
A | T | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+6880A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565045 | ||||||
chr9:105565096
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6931G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565096 | ||||||
chr9:105565125
|
C | A | 1 | a0002c0002t0004g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-181+6960C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565125 | ||||||
chr9:105565146
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+6981G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565146 | ||||||
chr9:105565170
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7005G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565170 | ||||||
chr9:105565174
|
A | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7009A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565174 | ||||||
chr9:105565182
|
C | T | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7017C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565182 | ||||||
chr9:105565183
|
T | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7018T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565183 | ||||||
chr9:105565187
|
C | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | NA18954.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-181+7022C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565187 | ||||||
chr9:105565192
|
A | T | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7027A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565192 | ||||||
chr9:105565200
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7035G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565200 | ||||||
chr9:105565202
|
T | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7037T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565202 | ||||||
chr9:105565204
|
C | G | 15 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(12): Show | 15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-181+7039C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565204 | ||||||
chr9:105565213
|
A | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7048A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565213 | ||||||
chr9:105565215
|
G | C | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7050G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565215 | ||||||
chr9:105565218
|
T | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7053T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565218 | ||||||
chr9:105565219
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7054G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565219 | ||||||
chr9:105565225
|
C | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7060C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565225 | ||||||
chr9:105565235
|
A | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7070A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565235 | ||||||
chr9:105565256
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+7091G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565256 | ||||||
chr9:105565300
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7135G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565300 | ||||||
chr9:105565306
|
C | T | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7141C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565306 | ||||||
chr9:105565321
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7156G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565321 | ||||||
chr9:105565328
|
G | T | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7163G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565328 | ||||||
chr9:105565330
|
C | T | 2 | a0001c0001t0001g0302a0001c0005t0019g0190 | 2 | HG01433.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-181+7165C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565330 | ||||||
chr9:105565335
|
G | T | 5 | a0001c0005t0019g0190a0001c0006t0014g0048a0001c0006t0014g0049others(2): Show | 5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-181+7170G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565335 | ||||||
chr9:105565384
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7219G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565384 | ||||||
chr9:105565411
|
A | G | 5 | a0001c0005t0019g0190a0001c0006t0014g0048a0001c0006t0014g0049others(2): Show | 5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-181+7246A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565411 | ||||||
chr9:105565416
|
A | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7251A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565416 | ||||||
chr9:105565441
|
G | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7276G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565441 | ||||||
chr9:105565485
|
T | C | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7320T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565485 | ||||||
chr9:105565509
|
A | T | 1 | a0001c0001t0001g0299 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-181+7344A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565509 | ||||||
chr9:105565554
|
G | T | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-181+7389G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565554 | ||||||
chr9:105565555
|
C | T | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-181+7390C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565555 | ||||||
chr9:105565601
|
G | A | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+7436G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565601 | ||||||
chr9:105565602
|
T | G | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+7437T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565602 | ||||||
chr9:105565604
|
T | C | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+7439T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565604 | ||||||
chr9:105565654
|
C | A | 1 | a0004c0004t0005g0038 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-181+7489C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565654 | ||||||
chr9:105565814
|
A | G | 1 | a0001c0001t0029g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-181+7649A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565814 | ||||||
chr9:105565892
|
T | A | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-181+7727T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565892 | ||||||
chr9:105565893
|
A | T | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-181+7728A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565893 | ||||||
chr9:105565912
|
C | G | 1 | a0003c0003t0001g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-180-7743C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565912 | ||||||
chr9:105565921
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-7734C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565921 | ||||||
chr9:105565947
|
G | A | 17 | a0002c0002t0004g0029a0002c0002t0004g0030a0002c0002t0004g0064others(14): Show | 19 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.-180-7708G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565947 | ||||||
chr9:105565987
|
T | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-7668T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565987 | ||||||
chr9:105566063
|
A | G | 21 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0165others(18): Show | 25 | HG00609.hp2 HG00642.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-180-7592A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566063 | ||||||
chr9:105566120
|
T | C | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-7535T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566120 | ||||||
chr9:105566305
|
G | A | 228 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(225): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.-180-7350G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566305 | ||||||
chr9:105566307
|
A | C | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-180-7348A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566307 | ||||||
chr9:105566355
|
T | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-7300T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566355 | ||||||
chr9:105566390
|
G | C | 3 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0062 | 3 | HG01255.hp2 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-7265G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566390 | ||||||
chr9:105566435
|
G | C | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01884.hp1 HG02723.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-7220G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566435 | ||||||
chr9:105566443
|
C | T | 2 | a0001c0001t0003g0101a0001c0001t0003g0102 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-180-7212C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566443 | ||||||
chr9:105566485
|
C | T | 1 | a0001c0001t0029g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-180-7170C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566485 | ||||||
chr9:105566541
|
C | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-180-7114C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566541 | ||||||
chr9:105566571
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-7084C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566571 | ||||||
chr9:105566606
|
A | T | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-7049A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566606 | ||||||
chr9:105566754
|
C | T | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-180-6901C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566754 | ||||||
chr9:105566761
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-180-6894C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566761 | ||||||
chr9:105566771
|
G | A | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-6884G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566771 | ||||||
chr9:105566778
|
C | T | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-180-6877C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566778 | ||||||
chr9:105566947
|
A | G | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-6708A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566947 | ||||||
chr9:105566993
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6662A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566993 | ||||||
chr9:105566995
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6660A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566995 | ||||||
chr9:105567076
|
G | A | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-180-6579G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567076 | ||||||
chr9:105567142
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-6513G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567142 | ||||||
chr9:105567158
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-180-6497A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567158 | ||||||
chr9:105567163
|
C | T | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-6492C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567163 | ||||||
chr9:105567183
|
C | A | 35 | a0002c0002t0004g0029a0002c0002t0004g0030a0002c0002t0004g0031others(32): Show | 40 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-180-6472C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567183 | ||||||
chr9:105567345
|
A | G | 5 | a0004c0004t0005g0038a0004c0004t0005g0039a0004c0004t0005g0040others(2): Show | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-6310A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567345 | ||||||
chr9:105567373
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6282T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567373 | ||||||
chr9:105567401
|
A | G | 2 | a0002c0002t0022g0203a0002c0002t0023g0204 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-180-6254A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567401 | ||||||
chr9:105567455
|
G | A | 1 | a0001c0001t0006g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-180-6200G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567455 | ||||||
chr9:105567598
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6057C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567598 | ||||||
chr9:105567631
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6024G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567631 | ||||||
chr9:105567760
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5895A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567760 | ||||||
chr9:105567790
|
ACTT | A | 3 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163 | 3 | HG02083.hp2 NA18990.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-180-5864_-180-586 others(7): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567790 | ||||||
chr9:105567810
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5845G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567810 | ||||||
chr9:105567829
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-180-5826G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567829 | ||||||
chr9:105567863
|
G | C | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-180-5792G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567863 | ||||||
chr9:105567871
|
A | G | 238 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0220others(235): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.-180-5784A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567871 | ||||||
chr9:105567872
|
C | T | 2 | a0001c0001t0005g0251a0001c0001t0006g0219 | 2 | HG03453.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-180-5783C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567872 | ||||||
chr9:105567873
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5782G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567873 | ||||||
chr9:105567951
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5704A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567951 | ||||||
chr9:105567951
|
A | T | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-180-5704A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567951 | ||||||
chr9:105567966
|
G | A | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-5689G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567966 | ||||||
chr9:105568164
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | NA18970.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-180-5491T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568164 | ||||||
chr9:105568376
|
T | A | 1 | a0001c0001t0012g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-180-5279T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568376 | ||||||
chr9:105568411
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-180-5244C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568411 | ||||||
chr9:105568425
|
A | T | 2 | a0001c0001t0038g0160a0001c0001t0039g0159 | 2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-180-5230A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568425 | ||||||
chr9:105568466
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5189C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568466 | ||||||
chr9:105568523
|
C | G | 5 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-180-5132C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568523 | ||||||
chr9:105568606
|
T | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5049T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568606 | ||||||
chr9:105568616
|
G | A | 1 | a0002c0002t0004g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-180-5039G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568616 | ||||||
chr9:105568666
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4989T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568666 | ||||||
chr9:105568678
|
T | C | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-4977T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568678 | ||||||
chr9:105568694
|
C | G | 1 | a0001c0001t0003g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-180-4961C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568694 | ||||||
chr9:105568731
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-180-4924C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568731 | ||||||
chr9:105568740
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4915T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568740 | ||||||
chr9:105568927
|
G | A | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-4728G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568927 | ||||||
chr9:105568953
|
G | A | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-180-4702G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568953 | ||||||
chr9:105569056
|
G | T | 2 | a0001c0001t0011g0209a0001c0001t0011g0210 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-180-4599G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569056 | ||||||
chr9:105569150
|
C | G | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-4505C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569150 | ||||||
chr9:105569161
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-180-4494C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569161 | ||||||
chr9:105569204
|
G | T | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-4451G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569204 | ||||||
chr9:105569253
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4402T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569253 | ||||||
chr9:105569525
|
T | G | 1 | a0001c0001t0029g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-180-4130T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569525 | ||||||
chr9:105569555
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4100A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569555 | ||||||
chr9:105569591
|
A | C | 2 | a0001c0001t0017g0018a0001c0001t0048g0088 | 3 | HG02071.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-180-4064A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569591 | ||||||
chr9:105569599
|
G | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4056G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569599 | ||||||
chr9:105569796
|
T | C | 91 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(88): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-180-3859T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569796 | ||||||
chr9:105570052
|
A | G | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-3603A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570052 | ||||||
chr9:105570142
|
C | CT | 8 | a0001c0001t0001g0297a0001c0006t0014g0048a0001c0006t0014g0049others(5): Show | 10 | HG00597.hp1 HG02004.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-180-3503dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105570142 | |||||
chr9:105570221
|
G | C | 3 | a0001c0001t0003g0020a0001c0001t0003g0092a0001c0001t0003g0093 | 4 | HG00597.hp2 HG02074.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-3434G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570221 | ||||||
chr9:105570333
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-3322C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570333 | ||||||
chr9:105570431
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-3224T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570431 | ||||||
chr9:105570742
|
T | G | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-2913T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570742 | ||||||
chr9:105570823
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-2832G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570823 | ||||||
chr9:105570922
|
G | A | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-180-2733G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570922 | ||||||
chr9:105570956
|
C | A | 1 | a0001c0001t0001g0042 | 2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-180-2699C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570956 | ||||||
chr9:105570973
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2682G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570973 | ||||||
chr9:105571038
|
A | G | 14 | a0001c0001t0002g0003a0001c0001t0002g0169a0001c0001t0002g0171others(11): Show | 17 | HG00642.hp2 HG01358.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-180-2617A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571038 | ||||||
chr9:105571057
|
A | G | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-2598A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571057 | ||||||
chr9:105571076
|
G | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2579G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571076 | ||||||
chr9:105571103
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-2552G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571103 | ||||||
chr9:105571167
|
A | G | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-180-2488A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571167 | ||||||
chr9:105571284
|
C | T | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-2371C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571284 | ||||||
chr9:105571309
|
G | A | 228 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(225): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.-180-2346G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571309 | ||||||
chr9:105571355
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2300C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571355 | ||||||
chr9:105571420
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2235T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571420 | ||||||
chr9:105571478
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2177G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571478 | ||||||
chr9:105571509
|
G | T | 1 | a0001c0001t0002g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-180-2146G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571509 | ||||||
chr9:105571616
|
C | T | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-2039C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571616 | ||||||
chr9:105571924
|
A | G | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-1731A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571924 | ||||||
chr9:105571971
|
G | A | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-1684G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571971 | ||||||
chr9:105572046
|
T | C | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-1609T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572046 | ||||||
chr9:105572064
|
A | C | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-180-1591A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572064 | ||||||
chr9:105572121
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1534C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572121 | ||||||
chr9:105572121
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1534C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572121 | ||||||
chr9:105572149
|
T | G | 2 | a0001c0001t0003g0015a0001c0001t0003g0089 | 3 | HG00323.hp1 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-180-1506T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572149 | ||||||
chr9:105572228
|
CTG | C | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1425_-180-142 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572228 | |||||
chr9:105572230
|
GTA | G | 171 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(168): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-180-1405_-180-140 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572230 | |||||
chr9:105572230
|
GTATA | G | 18 | a0001c0001t0005g0237a0001c0001t0005g0248a0001c0001t0005g0249others(15): Show | 18 | HG00280.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-180-1407_-180-140 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572230 | |||||
chr9:105572255
|
A | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1400A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572255 | ||||||
chr9:105572279
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-180-1376G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572279 | ||||||
chr9:105572317
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1338C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572317 | ||||||
chr9:105572338
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-1317G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572338 | ||||||
chr9:105572342
|
A | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-1313A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572342 | ||||||
chr9:105572406
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-180-1249T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572406 | ||||||
chr9:105572439
|
G | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1216G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572439 | ||||||
chr9:105572480
|
T | C | 4 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(1): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-180-1175T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572480 | ||||||
chr9:105572537
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-180-1118C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572537 | ||||||
chr9:105572601
|
C | G | 1 | a0001c0001t0003g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-180-1054C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572601 | ||||||
chr9:105572728
|
T | C | 5 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(2): Show | 5 | HG02040.hp1 HG02071.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-180-927T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572728 | ||||||
chr9:105572813
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-842C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572813 | ||||||
chr9:105572867
|
A | C | 2 | a0002c0002t0004g0191a0002c0002t0004g0208 | 2 | HG00735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-180-788A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572867 | ||||||
chr9:105572895
|
ATTTC | A | 13 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(10): Show | 14 | HG00673.hp2 HG02071.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.-180-753_-180-750d others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572895 | |||||
chr9:105572933
|
C | T | 35 | a0002c0002t0004g0029a0002c0002t0004g0030a0002c0002t0004g0031others(32): Show | 40 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-180-722C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572933 | ||||||
chr9:105572934
|
G | A | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-721G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572934 | ||||||
chr9:105572948
|
A | G | 62 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 75 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-180-707A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572948 | ||||||
chr9:105572971
|
A | T | 1 | a0001c0001t0002g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-180-684A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572971 | ||||||
chr9:105573063
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-592C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573063 | ||||||
chr9:105573077
|
A | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-578A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573077 | ||||||
chr9:105573215
|
A | C | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-440A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573215 | ||||||
chr9:105573219
|
A | G | 6 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(3): Show | 6 | HG01884.hp1 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-436A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573219 | ||||||
chr9:105573238
|
C | CA | 220 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(217): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.-180-406dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105573238 | |||||
chr9:105573238
|
C | CAA | 6 | a0001c0001t0002g0066a0001c0001t0002g0110a0001c0001t0003g0094others(3): Show | 8 | HG03098.hp2 NA18747.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-407_-180-406d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105573238 | |||||
chr9:105573260
|
T | C | 3 | a0001c0001t0003g0015a0001c0001t0003g0087a0001c0001t0003g0089 | 4 | HG00323.hp1 HG01361.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-395T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573260 | ||||||
chr9:105573312
|
A | G | 1 | a0001c0001t0016g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-180-343A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573312 | ||||||
chr9:105573413
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-242T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573413 | ||||||
chr9:105573427
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-228C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573427 | ||||||
chr9:105573463
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-180-192A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573463 | ||||||
chr9:105573495
|
G | C | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-180-160G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573495 | ||||||
chr9:105573550
|
T | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-105T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573550 | ||||||
chr9:105573553
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-102G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573553 | ||||||
chr9:105573553
|
G | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-102G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573553 | ||||||
chr9:105573554
|
G | C | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-101G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573554 | ||||||
chr9:105573589
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-180-66T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573589 | ||||||
chr9:105573606
|
C | T | 1 | a0002c0002t0004g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-180-49C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573606 | ||||||
chr9:105573627
|
C | CA | 11 | a0001c0001t0006g0243a0001c0001t0010g0053a0001c0001t0010g0054others(8): Show | 11 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-180-15dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105573627 | |||||
chr9:105573629
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0307 | 2 | NA19068.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-180-26A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573629 | ||||||
chr9:105573789
|
T | C | 49 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(46): Show | 62 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89+43T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573789 | ||||||
chr9:105573866
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0259a0001c0001t0001g0260others(7): Show | 13 | HG02080.hp1 NA18940.hp2 NA18954.hp1 others(10): Show |
intron_variant | MODIFIER | c.-89+120G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573866 | ||||||
chr9:105573867
|
T | C | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-89+121T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573867 | ||||||
chr9:105573989
|
A | G | 1 | a0001c0001t0047g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-89+243A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573989 | ||||||
chr9:105574395
|
A | G | 1 | a0001c0001t0002g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-88-550A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574395 | ||||||
chr9:105574466
|
A | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-479A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574466 | ||||||
chr9:105574601
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-344C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574601 | ||||||
chr9:105574698
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-88-247T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574698 | ||||||
chr9:105574752
|
A | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-88-193A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574752 | ||||||
chr9:105574813
|
T | G | 1 | a0001c0001t0006g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-88-132T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574813 | ||||||
chr9:105574835
|
T | A | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-110T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574835 | ||||||
chr9:105574939
|
T | C | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.-88-6T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574939 | ||||||
chr9:105575169
|
CCTTT | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+36_105+39delTC others(2): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105575169 | |||||
chr9:105575265
|
GC | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+129delC | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575265 | ||||||
chr9:105575563
|
A | C | 1 | a0001c0001t0001g0306 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.105+426A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575563 | ||||||
chr9:105575672
|
T | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+535T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575672 | ||||||
chr9:105575694
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+557G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575694 | ||||||
chr9:105575711
|
C | T | 1 | a0001c0005t0026g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+574C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575711 | ||||||
chr9:105575759
|
A | AT | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+622_105+623ins others(1): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575759 | ||||||
chr9:105575760
|
A | T | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+623A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575760 | ||||||
chr9:105575822
|
C | T | 1 | a0001c0001t0001g0047 | 2 | NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.105+685C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575822 | ||||||
chr9:105575876
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+739T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575876 | ||||||
chr9:105575920
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+783T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575920 | ||||||
chr9:105576038
|
A | T | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+901A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576038 | ||||||
chr9:105576090
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+953T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576090 | ||||||
chr9:105576101
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+964A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576101 | ||||||
chr9:105576132
|
A | G | 19 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0020others(16): Show | 24 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.105+995A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576132 | ||||||
chr9:105576145
|
CT | C | 51 | a0001c0001t0002g0028a0001c0001t0002g0111a0001c0001t0002g0112others(48): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.105+1024delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105576145 | |||||
chr9:105576149
|
T | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0092 | 3 | HG00597.hp2 NA18999.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.105+1012T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576149 | ||||||
chr9:105576170
|
T | A | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1033T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576170 | ||||||
chr9:105576192
|
G | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 5 | HG00099.hp1 HG00280.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1055G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576192 | ||||||
chr9:105576206
|
T | G | 5 | a0001c0001t0001g0259a0001c0006t0014g0048a0001c0006t0014g0049others(2): Show | 5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1069T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576206 | ||||||
chr9:105576300
|
A | G | 1 | a0002c0002t0023g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.105+1163A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576300 | ||||||
chr9:105576337
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1200T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576337 | ||||||
chr9:105576388
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1251T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576388 | ||||||
chr9:105576413
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0220 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.105+1276C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576413 | ||||||
chr9:105576435
|
A | G | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+1298A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576435 | ||||||
chr9:105576490
|
C | T | 1 | a0002c0002t0004g0194 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.105+1353C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576490 | ||||||
chr9:105576616
|
C | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1479C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576616 | ||||||
chr9:105576626
|
A | G | 1 | a0002c0002t0004g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.105+1489A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576626 | ||||||
chr9:105576631
|
T | G | 5 | a0001c0001t0003g0090a0001c0001t0012g0059a0001c0001t0012g0060others(2): Show | 5 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1494T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576631 | ||||||
chr9:105576667
|
A | C | 5 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(2): Show | 5 | HG02723.hp2 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+1530A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576667 | ||||||
chr9:105576735
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0220 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.105+1598A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576735 | ||||||
chr9:105576886
|
T | A | 3 | a0001c0006t0014g0048a0001c0006t0014g0049a0008c0009t0015g0050 | 3 | HG03471.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.105+1749T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576886 | ||||||
chr9:105576946
|
T | G | 28 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(25): Show | 35 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.105+1809T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576946 | ||||||
chr9:105576994
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1857C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576994 | ||||||
chr9:105576995
|
G | A | 1 | a0001c0001t0045g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.105+1858G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576995 | ||||||
chr9:105577014
|
G | T | 136 | a0001c0001t0002g0154a0001c0001t0003g0001a0001c0001t0003g0005others(133): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.105+1877G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577014 | ||||||
chr9:105577048
|
A | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1911A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577048 | ||||||
chr9:105577093
|
A | G | 8 | a0001c0001t0006g0221a0001c0001t0006g0223a0001c0001t0018g0222others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+1956A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577093 | ||||||
chr9:105577109
|
T | G | 4 | a0001c0001t0006g0221a0001c0001t0006g0223a0001c0001t0018g0222others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+1972T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577109 | ||||||
chr9:105577206
|
C | T | 1 | a0001c0001t0002g0177 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.105+2069C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577206 | ||||||
chr9:105577207
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2070T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577207 | ||||||
chr9:105577211
|
G | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2074G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577211 | ||||||
chr9:105577217
|
G | A | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+2080G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577217 | ||||||
chr9:105577225
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2088G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577225 | ||||||
chr9:105577308
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0177 | 2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.105+2171C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577308 | ||||||
chr9:105577339
|
T | C | 1 | a0001c0001t0032g0113 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.105+2202T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577339 | ||||||
chr9:105577410
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2273A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577410 | ||||||
chr9:105577414
|
A | G | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.105+2277A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577414 | ||||||
chr9:105577440
|
T | G | 15 | a0001c0001t0005g0251a0001c0001t0010g0053a0001c0001t0010g0054others(12): Show | 15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.105+2303T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577440 | ||||||
chr9:105577481
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2344G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577481 | ||||||
chr9:105577486
|
C | T | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+2349C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577486 | ||||||
chr9:105577487
|
G | A | 1 | a0003c0003t0001g0225 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.105+2350G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577487 | ||||||
chr9:105577497
|
C | G | 1 | a0003c0003t0028g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.105+2360C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577497 | ||||||
chr9:105577565
|
A | C | 47 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(44): Show | 53 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.105+2428A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577565 | ||||||
chr9:105577577
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2440T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577577 | ||||||
chr9:105577591
|
G | C | 2 | a0001c0001t0002g0111a0001c0001t0002g0114 | 2 | HG00140.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.105+2454G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577591 | ||||||
chr9:105577600
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2463C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577600 | ||||||
chr9:105577668
|
C | A | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+2531C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577668 | ||||||
chr9:105577728
|
G | C | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+2591G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577728 | ||||||
chr9:105577787
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2650C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577787 | ||||||
chr9:105577810
|
G | A | 1 | a0001c0001t0006g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.105+2673G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577810 | ||||||
chr9:105577843
|
C | G | 1 | a0002c0002t0020g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.105+2706C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577843 | ||||||
chr9:105577853
|
G | C | 1 | a0001c0001t0001g0255 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.105+2716G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577853 | ||||||
chr9:105577934
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2797A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577934 | ||||||
chr9:105577940
|
A | G | 229 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(226): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.105+2803A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577940 | ||||||
chr9:105577949
|
C | G | 1 | a0002c0002t0001g0294 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.105+2812C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577949 | ||||||
chr9:105578025
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2888T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578025 | ||||||
chr9:105578062
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.105+2925A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578062 | ||||||
chr9:105578107
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.105+2970G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578107 | ||||||
chr9:105578124
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2987G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578124 | ||||||
chr9:105578339
|
G | A | 1 | a0001c0001t0033g0170 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.105+3202G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578339 | ||||||
chr9:105578384
|
T | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+3247T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578384 | ||||||
chr9:105578488
|
A | C | 40 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0019g0190others(37): Show | 46 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.105+3351A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578488 | ||||||
chr9:105578509
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+3372A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578509 | ||||||
chr9:105578612
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.105+3475A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578612 | ||||||
chr9:105578730
|
G | A | 1 | a0001c0001t0034g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.105+3593G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578730 | ||||||
chr9:105578778
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02040.hp1 NA18612.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+3641C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578778 | ||||||
chr9:105578842
|
T | A | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.105+3705T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578842 | ||||||
chr9:105578871
|
A | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+3734A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578871 | ||||||
chr9:105578907
|
A | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+3770A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578907 | ||||||
chr9:105578936
|
A | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA18969.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.105+3799A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578936 | ||||||
chr9:105578947
|
T | C | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+3810T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578947 | ||||||
chr9:105578993
|
A | G | 39 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(36): Show | 44 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.105+3856A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578993 | ||||||
chr9:105578995
|
T | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0307 | 2 | NA19068.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.105+3858T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578995 | ||||||
chr9:105579023
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.105+3886G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579023 | ||||||
chr9:105579034
|
C | T | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.105+3897C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579034 | ||||||
chr9:105579035
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0016g0117a0001c0001t0016g0156 | 3 | HG02602.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.105+3898G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579035 | ||||||
chr9:105579037
|
C | G | 3 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0030g0151 | 3 | NA18970.hp2 NA18999.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.105+3900C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579037 | ||||||
chr9:105579043
|
C | G | 6 | a0001c0001t0046g0057a0001c0006t0014g0048a0001c0006t0014g0049others(3): Show | 6 | HG02723.hp2 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+3906C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579043 | ||||||
chr9:105579142
|
T | G | 229 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(226): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.105+4005T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579142 | ||||||
chr9:105579235
|
C | G | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4098C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579235 | ||||||
chr9:105579237
|
A | C | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+4100A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579237 | ||||||
chr9:105579338
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4201C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579338 | ||||||
chr9:105579339
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4202A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579339 | ||||||
chr9:105579362
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.105+4225C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579362 | ||||||
chr9:105579376
|
C | T | 3 | a0003c0003t0001g0238a0003c0003t0001g0239a0003c0003t0001g0240 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.105+4239C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579376 | ||||||
chr9:105579415
|
C | T | 1 | a0001c0001t0003g0015 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.105+4278C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579415 | ||||||
chr9:105579471
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4334C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579471 | ||||||
chr9:105579485
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4348T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579485 | ||||||
chr9:105579492
|
A | C | 2 | a0001c0001t0003g0101a0001c0001t0003g0102 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.105+4355A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579492 | ||||||
chr9:105579588
|
A | T | 1 | a0001c0001t0006g0312 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.105+4451A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579588 | ||||||
chr9:105579737
|
C | T | 4 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(1): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+4600C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579737 | ||||||
chr9:105579756
|
G | A | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.105+4619G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579756 | ||||||
chr9:105579767
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+4630G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579767 | ||||||
chr9:105579799
|
C | G | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4662C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579799 | ||||||
chr9:105579820
|
A | T | 1 | a0002c0002t0020g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.105+4683A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579820 | ||||||
chr9:105579821
|
C | T | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.105+4684C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579821 | ||||||
chr9:105579845
|
T | G | 1 | a0002c0002t0001g0272 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.105+4708T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579845 | ||||||
chr9:105579869
|
A | G | 5 | a0002c0002t0001g0272a0002c0002t0001g0287a0002c0002t0001g0288others(2): Show | 5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+4732A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579869 | ||||||
chr9:105580072
|
G | C | 3 | a0001c0001t0011g0205a0001c0001t0011g0209a0001c0001t0011g0210 | 3 | HG02486.hp1 HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.105+4935G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580072 | ||||||
chr9:105580094
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4957T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580094 | ||||||
chr9:105580099
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4962G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580099 | ||||||
chr9:105580121
|
A | G | 4 | a0001c0001t0002g0026a0001c0001t0002g0148a0001c0001t0046g0057others(1): Show | 5 | HG00323.hp2 HG01255.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+4984A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580121 | ||||||
chr9:105580126
|
C | A | 12 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(9): Show | 12 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+4989C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580126 | ||||||
chr9:105580170
|
A | G | 1 | a0001c0001t0047g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.105+5033A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580170 | ||||||
chr9:105580265
|
C | T | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+5128C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580265 | ||||||
chr9:105580332
|
T | C | 2 | a0002c0002t0004g0191a0002c0002t0004g0208 | 2 | HG00735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.105+5195T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580332 | ||||||
chr9:105580406
|
A | T | 91 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(88): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.105+5269A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580406 | ||||||
chr9:105580534
|
C | T | 2 | a0005c0007t0005g0035a0005c0007t0005g0242 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.105+5397C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580534 | ||||||
chr9:105580542
|
A | G | 49 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(46): Show | 62 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.105+5405A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580542 | ||||||
chr9:105580576
|
C | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+5439C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580576 | ||||||
chr9:105580596
|
A | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0304 | 2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.105+5459A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580596 | ||||||
chr9:105580662
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.105+5525G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580662 | ||||||
chr9:105580668
|
T | G | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0008c0009t0015g0050 | 4 | HG02109.hp2 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5531T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580668 | ||||||
chr9:105580689
|
A | G | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.105+5552A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580689 | ||||||
chr9:105580787
|
A | G | 1 | a0001c0001t0002g0026 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.105+5650A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580787 | ||||||
chr9:105580859
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5722C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580859 | ||||||
chr9:105580900
|
G | A | 1 | a0001c0001t0042g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.105+5763G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580900 | ||||||
chr9:105580954
|
C | T | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+5817C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580954 | ||||||
chr9:105581016
|
A | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+5879A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581016 | ||||||
chr9:105581031
|
T | C | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+5894T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581031 | ||||||
chr9:105581036
|
C | T | 1 | a0001c0001t0027g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+5899C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581036 | ||||||
chr9:105581081
|
A | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5944A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581081 | ||||||
chr9:105581089
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5952T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581089 | ||||||
chr9:105581143
|
G | T | 57 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(54): Show | 70 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.105+6006G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581143 | ||||||
chr9:105581168
|
G | A | 49 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(46): Show | 63 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.105+6031G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581168 | ||||||
chr9:105581177
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6040A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581177 | ||||||
chr9:105581197
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6060C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581197 | ||||||
chr9:105581198
|
C | T | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+6061C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581198 | ||||||
chr9:105581227
|
T | G | 1 | a0001c0005t0026g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+6090T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581227 | ||||||
chr9:105581240
|
G | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(57): Show | 72 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.105+6103G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581240 | ||||||
chr9:105581240
|
G | C | 2 | a0001c0001t0003g0017a0001c0001t0003g0086 | 3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.105+6103G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581240 | ||||||
chr9:105581241
|
C | G | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6104C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581241 | ||||||
chr9:105581312
|
T | A | 1 | a0001c0001t0003g0082 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.105+6175T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581312 | ||||||
chr9:105581331
|
A | T | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.105+6194A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581331 | ||||||
chr9:105581391
|
G | C | 1 | a0001c0001t0003g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.105+6254G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581391 | ||||||
chr9:105581402
|
G | T | 1 | a0001c0001t0027g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+6265G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581402 | ||||||
chr9:105581416
|
G | A | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+6279G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581416 | ||||||
chr9:105581418
|
A | G | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+6281A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581418 | ||||||
chr9:105581426
|
T | G | 1 | a0001c0001t0003g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.105+6289T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581426 | ||||||
chr9:105581445
|
C | T | 3 | a0002c0002t0004g0185a0002c0002t0004g0187a0002c0002t0004g0212 | 3 | HG00741.hp2 HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.105+6308C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581445 | ||||||
chr9:105581453
|
C | G | 35 | a0001c0001t0002g0147a0001c0001t0003g0006a0001c0001t0003g0100others(32): Show | 45 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.105+6316C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581453 | ||||||
chr9:105581512
|
C | T | 1 | a0001c0001t0016g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.105+6375C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581512 | ||||||
chr9:105581521
|
G | C | 7 | a0001c0001t0002g0118a0001c0001t0032g0113a0001c0006t0014g0048others(4): Show | 7 | HG00621.hp1 HG02148.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+6384G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581521 | ||||||
chr9:105581521
|
G | T | 4 | a0001c0001t0003g0017a0001c0001t0003g0086a0001c0001t0038g0160others(1): Show | 5 | HG02155.hp1 NA18945.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+6384G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581521 | ||||||
chr9:105581584
|
G | T | 1 | a0001c0001t0042g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.105+6447G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581584 | ||||||
chr9:105581678
|
A | G | 5 | a0002c0002t0001g0272a0002c0002t0001g0287a0002c0002t0001g0288others(2): Show | 5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+6541A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581678 | ||||||
chr9:105581680
|
T | C | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+6543T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581680 | ||||||
chr9:105581694
|
T | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+6557T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581694 | ||||||
chr9:105581710
|
C | A | 1 | a0002c0002t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.105+6573C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581710 | ||||||
chr9:105581710
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6573C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581710 | ||||||
chr9:105581747
|
C | T | 1 | a0002c0002t0004g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.105+6610C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581747 | ||||||
chr9:105581763
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.105+6626A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581763 | ||||||
chr9:105581770
|
C | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+6633C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581770 | ||||||
chr9:105581790
|
C | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+6653C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581790 | ||||||
chr9:105581794
|
G | C | 1 | a0001c0005t0026g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+6657G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581794 | ||||||
chr9:105581802
|
G | T | 13 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(10): Show | 13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+6665G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581802 | ||||||
chr9:105581823
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.105+6686C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581823 | ||||||
chr9:105581846
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6709C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581846 | ||||||
chr9:105581854
|
G | A | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+6717G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581854 | ||||||
chr9:105581875
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6738T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581875 | ||||||
chr9:105582008
|
C | T | 1 | a0001c0001t0012g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.105+6871C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582008 | ||||||
chr9:105582038
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.105+6901G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582038 | ||||||
chr9:105582039
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.105+6902C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582039 | ||||||
chr9:105582044
|
C | A | 8 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(5): Show | 8 | HG01255.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+6907C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582044 | ||||||
chr9:105582049
|
A | G | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+6912A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582049 | ||||||
chr9:105582055
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.105+6918C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582055 | ||||||
chr9:105582085
|
G | T | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+6948G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582085 | ||||||
chr9:105582095
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6958C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582095 | ||||||
chr9:105582122
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0291 | 2 | HG00621.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.105+6985G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582122 | ||||||
chr9:105582139
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7002T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582139 | ||||||
chr9:105582159
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0283a0001c0001t0001g0292others(1): Show | 5 | NA18969.hp2 NA18982.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+7022A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582159 | ||||||
chr9:105582228
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7091G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582228 | ||||||
chr9:105582247
|
A | G | 3 | a0003c0003t0001g0238a0003c0003t0001g0239a0003c0003t0001g0240 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.105+7110A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582247 | ||||||
chr9:105582269
|
G | A | 1 | a0002c0002t0025g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.105+7132G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582269 | ||||||
chr9:105582279
|
A | AC | 198 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(195): Show | 228 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.105+7142_105+7143i others(3): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582279 | ||||||
chr9:105582321
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.105+7184G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582321 | ||||||
chr9:105582333
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7196A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582333 | ||||||
chr9:105582335
|
A | T | 1 | a0001c0001t0003g0086 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.105+7198A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582335 | ||||||
chr9:105582350
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7213C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582350 | ||||||
chr9:105582351
|
G | A | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+7214G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582351 | ||||||
chr9:105582471
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7334C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582471 | ||||||
chr9:105582482
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7345T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582482 | ||||||
chr9:105582538
|
C | A | 2 | a0001c0005t0013g0032a0001c0005t0013g0181 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.105+7401C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582538 | ||||||
chr9:105582538
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7401C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582538 | ||||||
chr9:105582638
|
A | G | 1 | a0001c0001t0003g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.105+7501A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582638 | ||||||
chr9:105582737
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.105+7600A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582737 | ||||||
chr9:105582739
|
T | A | 1 | a0001c0001t0011g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.105+7602T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582739 | ||||||
chr9:105582829
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7692C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582829 | ||||||
chr9:105582931
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7794A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582931 | ||||||
chr9:105583213
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8076C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583213 | ||||||
chr9:105583388
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+8251C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583388 | ||||||
chr9:105583413
|
A | G | 9 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(6): Show | 9 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+8276A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583413 | ||||||
chr9:105583493
|
G | C | 1 | a0001c0001t0003g0084 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.105+8356G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583493 | ||||||
chr9:105583594
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.105+8457T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583594 | ||||||
chr9:105583641
|
G | A | 2 | a0005c0007t0005g0035a0005c0007t0005g0242 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.105+8504G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583641 | ||||||
chr9:105583726
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8589A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583726 | ||||||
chr9:105583849
|
A | G | 2 | a0001c0001t0012g0059a0001c0001t0012g0060 | 2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.105+8712A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583849 | ||||||
chr9:105583885
|
C | G | 1 | a0001c0006t0014g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.105+8748C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583885 | ||||||
chr9:105583890
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8753T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583890 | ||||||
chr9:105583900
|
A | G | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+8763A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583900 | ||||||
chr9:105583984
|
G | A | 1 | a0001c0001t0029g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.105+8847G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583984 | ||||||
chr9:105584098
|
A | G | 1 | a0001c0001t0016g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.105+8961A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584098 | ||||||
chr9:105584162
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+9025A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584162 | ||||||
chr9:105584460
|
A | G | 1 | a0003c0003t0004g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.105+9323A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584460 | ||||||
chr9:105584649
|
A | C | 1 | a0002c0011t0004g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.105+9512A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584649 | ||||||
chr9:105584789
|
C | G | 1 | a0001c0001t0001g0269 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.105+9652C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584789 | ||||||
chr9:105584794
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.105+9657C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584794 | ||||||
chr9:105584858
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0177 | 2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.105+9721C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584858 | ||||||
chr9:105584859
|
G | A | 1 | a0003c0003t0001g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.105+9722G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584859 | ||||||
chr9:105584868
|
C | G | 1 | a0001c0001t0002g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.105+9731C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584868 | ||||||
chr9:105584869
|
C | T | 1 | a0001c0001t0030g0151 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.105+9732C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584869 | ||||||
chr9:105584891
|
G | T | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+9754G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584891 | ||||||
chr9:105584932
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.105+9795A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584932 | ||||||
chr9:105584984
|
G | C | 1 | a0001c0001t0002g0120 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.105+9847G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584984 | ||||||
chr9:105585117
|
G | GA | 44 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(41): Show | 50 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.105+9989dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105585117 | |||||
chr9:105585238
|
A | G | 1 | a0001c0001t0010g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.105+10101A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585238 | ||||||
chr9:105585433
|
T | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0179 | 2 | NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.105+10296T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585433 | ||||||
chr9:105585613
|
A | G | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.105+10476A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585613 | ||||||
chr9:105585857
|
G | A | 35 | a0002c0002t0004g0029a0002c0002t0004g0030a0002c0002t0004g0031others(32): Show | 40 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.105+10720G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585857 | ||||||
chr9:105585858
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.105+10721C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585858 | ||||||
chr9:105585919
|
A | G | 1 | a0001c0001t0033g0170 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106-10679A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585919 | ||||||
chr9:105586023
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.106-10575G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586023 | ||||||
chr9:105586056
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10542C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586056 | ||||||
chr9:105586127
|
C | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-10471C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586127 | ||||||
chr9:105586142
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10456G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586142 | ||||||
chr9:105586145
|
G | A | 1 | a0003c0003t0001g0227 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.106-10453G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586145 | ||||||
chr9:105586176
|
C | T | 2 | a0001c0001t0011g0209a0001c0001t0011g0210 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.106-10422C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586176 | ||||||
chr9:105586201
|
TATC | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10394_106-1039 others(7): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105586201 | |||||
chr9:105586229
|
T | TAGTA | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10368_106-1036 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105586229 | |||||
chr9:105586233
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG00558.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.106-10365A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586233 | ||||||
chr9:105586253
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10345A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586253 | ||||||
chr9:105586524
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.106-10074G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586524 | ||||||
chr9:105586578
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10020A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586578 | ||||||
chr9:105586608
|
C | T | 317 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(314): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.106-9990C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586608 | ||||||
chr9:105586632
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-9966A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586632 | ||||||
chr9:105586659
|
G | A | 5 | a0004c0004t0005g0038a0004c0004t0005g0039a0004c0004t0005g0040others(2): Show | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-9939G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586659 | ||||||
chr9:105586790
|
A | T | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.106-9808A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586790 | ||||||
chr9:105586950
|
G | C | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.106-9648G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586950 | ||||||
chr9:105587071
|
A | T | 1 | a0003c0003t0001g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.106-9527A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587071 | ||||||
chr9:105587353
|
G | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-9245G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587353 | ||||||
chr9:105587773
|
C | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.106-8825C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587773 | ||||||
chr9:105587809
|
T | C | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0121others(1): Show | 5 | NA18953.hp1 NA18968.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-8789T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587809 | ||||||
chr9:105587835
|
G | A | 1 | a0002c0002t0004g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-8763G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587835 | ||||||
chr9:105587890
|
G | A | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-8708G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587890 | ||||||
chr9:105587900
|
G | A | 228 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(225): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.106-8698G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587900 | ||||||
chr9:105588002
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-8596A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588002 | ||||||
chr9:105588047
|
T | A | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-8551T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588047 | ||||||
chr9:105588113
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.106-8485C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588113 | ||||||
chr9:105588360
|
AT | A | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-8229delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105588360 | |||||
chr9:105588373
|
C | G | 1 | a0001c0001t0003g0078 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.106-8225C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588373 | ||||||
chr9:105588446
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-8152G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588446 | ||||||
chr9:105588549
|
G | C | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-8049G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588549 | ||||||
chr9:105588799
|
C | G | 2 | a0001c0001t0012g0059a0001c0001t0012g0060 | 2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.106-7799C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588799 | ||||||
chr9:105588952
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-7646C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588952 | ||||||
chr9:105589082
|
A | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-7516A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589082 | ||||||
chr9:105589215
|
C | T | 1 | a0001c0001t0006g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.106-7383C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589215 | ||||||
chr9:105589459
|
G | A | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.106-7139G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589459 | ||||||
chr9:105589521
|
C | CG | 7 | a0001c0001t0002g0119a0001c0001t0002g0122a0001c0001t0006g0221others(4): Show | 7 | HG00735.hp1 HG01243.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-7074dupG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105589521 | |||||
chr9:105589521
|
C | G | 2 | a0001c0001t0012g0062a0002c0002t0004g0183 | 2 | HG02027.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.106-7077C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589521 | ||||||
chr9:105589521
|
C | T | 3 | a0004c0004t0005g0038a0004c0004t0005g0040a0004c0004t0005g0252 | 5 | HG01099.hp2 HG01167.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-7077C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589521 | ||||||
chr9:105589529
|
A | G | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-7069A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589529 | ||||||
chr9:105589535
|
A | T | 39 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0019g0190others(36): Show | 45 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.106-7063A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589535 | ||||||
chr9:105589631
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6967G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589631 | ||||||
chr9:105589696
|
G | T | 2 | a0001c0005t0013g0032a0001c0005t0013g0181 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.106-6902G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589696 | ||||||
chr9:105589858
|
G | C | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-6740G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589858 | ||||||
chr9:105589934
|
G | A | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-6664G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589934 | ||||||
chr9:105589934
|
G | C | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-6664G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589934 | ||||||
chr9:105589969
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6629G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589969 | ||||||
chr9:105589974
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6624A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589974 | ||||||
chr9:105590067
|
C | T | 241 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(238): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.106-6531C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590067 | ||||||
chr9:105590093
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | NA18973.hp2 NA19056.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.106-6505G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590093 | ||||||
chr9:105590106
|
C | T | 2 | a0002c0002t0022g0203a0002c0002t0023g0204 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.106-6492C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590106 | ||||||
chr9:105590142
|
C | G | 1 | a0002c0002t0008g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.106-6456C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590142 | ||||||
chr9:105590151
|
G | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-6447G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590151 | ||||||
chr9:105590192
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6406C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590192 | ||||||
chr9:105590319
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0259a0001c0001t0001g0260others(6): Show | 12 | HG02080.hp1 NA18954.hp1 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.106-6279T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590319 | ||||||
chr9:105590568
|
A | C | 2 | a0001c0006t0015g0051a0008c0009t0015g0050 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.106-6030A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590568 | ||||||
chr9:105590716
|
GT | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5875delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105590716 | |||||
chr9:105590727
|
C | T | 1 | a0001c0001t0042g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.106-5871C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590727 | ||||||
chr9:105590883
|
G | A | 1 | a0002c0002t0004g0064 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.106-5715G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590883 | ||||||
chr9:105590898
|
AC | A | 43 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-5699delC | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590898 | ||||||
chr9:105590922
|
G | A | 31 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(28): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.106-5676G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590922 | ||||||
chr9:105590929
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5669G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590929 | ||||||
chr9:105590932
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.106-5666C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590932 | ||||||
chr9:105591217
|
A | G | 197 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(194): Show | 227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.106-5381A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591217 | ||||||
chr9:105591237
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5361C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591237 | ||||||
chr9:105591311
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5287C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591311 | ||||||
chr9:105591373
|
G | A | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-5225G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591373 | ||||||
chr9:105591433
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5165G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591433 | ||||||
chr9:105591586
|
C | G | 5 | a0002c0002t0001g0272a0002c0002t0001g0287a0002c0002t0001g0288others(2): Show | 5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-5012C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591586 | ||||||
chr9:105591647
|
G | C | 13 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(10): Show | 13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.106-4951G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591647 | ||||||
chr9:105591896
|
C | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4702C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591896 | ||||||
chr9:105591949
|
C | T | 210 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(207): Show | 240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.106-4649C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591949 | ||||||
chr9:105592031
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4567A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592031 | ||||||
chr9:105592120
|
G | T | 318 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(315): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.106-4478G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592120 | ||||||
chr9:105592136
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.106-4462C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592136 | ||||||
chr9:105592215
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4383A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592215 | ||||||
chr9:105592216
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4382A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592216 | ||||||
chr9:105592404
|
C | T | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.106-4194C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592404 | ||||||
chr9:105592405
|
G | T | 2 | a0005c0007t0005g0035a0005c0007t0005g0242 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.106-4193G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592405 | ||||||
chr9:105592439
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4159T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592439 | ||||||
chr9:105592519
|
C | A | 1 | a0001c0001t0006g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.106-4079C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592519 | ||||||
chr9:105592653
|
G | T | 1 | a0001c0001t0003g0100 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.106-3945G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592653 | ||||||
chr9:105592688
|
C | G | 1 | a0003c0003t0001g0230 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106-3910C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592688 | ||||||
chr9:105592749
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3849A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592749 | ||||||
chr9:105592767
|
CT | C | 13 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(10): Show | 13 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.106-3826delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105592767 | |||||
chr9:105592941
|
T | C | 210 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(207): Show | 240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.106-3657T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592941 | ||||||
chr9:105592954
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.106-3644A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592954 | ||||||
chr9:105593014
|
A | C | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-3584A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593014 | ||||||
chr9:105593040
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3558A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593040 | ||||||
chr9:105593130
|
A | C | 2 | a0001c0001t0003g0076a0001c0001t0003g0077 | 2 | NA19004.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.106-3468A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593130 | ||||||
chr9:105593333
|
C | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3265C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593333 | ||||||
chr9:105593333
|
C | T | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.106-3265C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593333 | ||||||
chr9:105593352
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-3246C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593352 | ||||||
chr9:105593470
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0220 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.106-3128A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593470 | ||||||
chr9:105593556
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3042C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593556 | ||||||
chr9:105593804
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106-2794A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593804 | ||||||
chr9:105593814
|
A | C | 6 | a0001c0001t0006g0014a0001c0001t0006g0037a0001c0001t0006g0052others(3): Show | 9 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.106-2784A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593814 | ||||||
chr9:105593818
|
T | C | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.106-2780T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593818 | ||||||
chr9:105594109
|
C | A | 9 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(6): Show | 9 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.106-2489C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594109 | ||||||
chr9:105594341
|
G | A | 5 | a0001c0001t0006g0246a0001c0006t0014g0048a0001c0006t0014g0049others(2): Show | 5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.106-2257G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594341 | ||||||
chr9:105594437
|
C | A | 1 | a0002c0002t0024g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.106-2161C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594437 | ||||||
chr9:105594522
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-2076C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594522 | ||||||
chr9:105594695
|
G | A | 3 | a0002c0002t0022g0203a0002c0002t0023g0204a0009c0014t0043g0067 | 3 | HG02280.hp2 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.106-1903G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594695 | ||||||
chr9:105594840
|
G | A | 2 | a0001c0006t0015g0051a0008c0009t0015g0050 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.106-1758G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594840 | ||||||
chr9:105594955
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1643A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594955 | ||||||
chr9:105594969
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1629T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594969 | ||||||
chr9:105595086
|
C | T | 1 | a0001c0001t0003g0096 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.106-1512C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595086 | ||||||
chr9:105595143
|
A | G | 4 | a0001c0001t0003g0016a0001c0001t0003g0019a0001c0001t0003g0080others(1): Show | 6 | HG00741.hp1 HG01099.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-1455A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595143 | ||||||
chr9:105595231
|
T | C | 60 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(57): Show | 66 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.106-1367T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595231 | ||||||
chr9:105595425
|
G | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.106-1173G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595425 | ||||||
chr9:105595634
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-964C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595634 | ||||||
chr9:105595702
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-896A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595702 | ||||||
chr9:105595718
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.106-880G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595718 | ||||||
chr9:105595729
|
T | C | 1 | a0002c0002t0001g0270 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.106-869T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595729 | ||||||
chr9:105595730
|
C | T | 1 | a0002c0002t0001g0270 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.106-868C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595730 | ||||||
chr9:105595850
|
C | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.106-748C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595850 | ||||||
chr9:105596004
|
C | T | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-594C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596004 | ||||||
chr9:105596040
|
A | C | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-558A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596040 | ||||||
chr9:105596051
|
CG | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-546delG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596051 | ||||||
chr9:105596065
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-533C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596065 | ||||||
chr9:105596071
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.106-527G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596071 | ||||||
chr9:105596079
|
T | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-519T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596079 | ||||||
chr9:105596117
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-481C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596117 | ||||||
chr9:105596137
|
A | C | 1 | a0001c0001t0002g0144 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106-461A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596137 | ||||||
chr9:105596249
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-349A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596249 | ||||||
chr9:105596353
|
C | T | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-245C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596353 | ||||||
chr9:105596429
|
A | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-169A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596429 | ||||||
chr9:105596558
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-40A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596558 | ||||||
chr9:105596588
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596588 | ||||||
chr9:105596686
|
A | G | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165+29A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596686 | ||||||
chr9:105596720
|
G | T | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165+63G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596720 | ||||||
chr9:105596776
|
G | A | 1 | a0001c0005t0026g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+119G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596776 | ||||||
chr9:105596871
|
T | A | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165+214T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596871 | ||||||
chr9:105597084
|
A | T | 1 | a0002c0002t0025g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165+427A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597084 | ||||||
chr9:105597193
|
C | T | 2 | a0001c0001t0003g0101a0001c0001t0003g0102 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.165+536C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597193 | ||||||
chr9:105597258
|
C | A | 95 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(92): Show | 106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.165+601C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597258 | ||||||
chr9:105597461
|
A | C | 3 | a0001c0001t0002g0023a0001c0001t0002g0121a0001c0015t0002g0023 | 3 | NA18953.hp1 NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.165+804A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597461 | ||||||
chr9:105597659
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+1002C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597659 | ||||||
chr9:105597668
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.165+1011C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597668 | ||||||
chr9:105597919
|
G | A | 13 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(10): Show | 13 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+1262G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597919 | ||||||
chr9:105597920
|
G | A | 1 | a0002c0002t0025g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165+1263G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597920 | ||||||
chr9:105597975
|
G | A | 1 | a0001c0001t0035g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.165+1318G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597975 | ||||||
chr9:105597976
|
C | G | 1 | a0001c0001t0035g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.165+1319C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597976 | ||||||
chr9:105598069
|
T | C | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165+1412T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598069 | ||||||
chr9:105598284
|
A | G | 2 | a0005c0007t0005g0035a0005c0007t0005g0242 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.165+1627A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598284 | ||||||
chr9:105598423
|
A | G | 3 | a0001c0001t0002g0143a0001c0001t0038g0160a0001c0001t0039g0159 | 3 | NA18945.hp1 NA18957.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.165+1766A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598423 | ||||||
chr9:105598466
|
G | T | 2 | a0005c0007t0005g0035a0005c0007t0005g0242 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.165+1809G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598466 | ||||||
chr9:105598537
|
A | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+1880A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598537 | ||||||
chr9:105598816
|
T | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+2159T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598816 | ||||||
chr9:105598839
|
T | G | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2182T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598839 | ||||||
chr9:105598932
|
G | GAC | 7 | a0001c0001t0003g0076a0001c0001t0003g0077a0001c0001t0010g0053others(4): Show | 7 | HG01884.hp1 HG02818.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-2193_166-2192d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105598932 | |||||
chr9:105598932
|
GAC | G | 146 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(143): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.166-2193_166-2192d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105598932 | |||||
chr9:105599091
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.166-2054T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599091 | ||||||
chr9:105599215
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0280a0001c0001t0001g0305others(1): Show | 6 | HG01109.hp1 HG01952.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1930T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599215 | ||||||
chr9:105599475
|
C | CT | 51 | a0001c0001t0001g0034a0001c0001t0001g0220a0001c0001t0002g0121others(48): Show | 57 | HG00323.hp1 HG00673.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.166-1652dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599475 | |||||
chr9:105599475
|
C | CTT | 25 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(22): Show | 33 | HG00558.hp1 HG00609.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.166-1653_166-1652d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599475 | |||||
chr9:105599475
|
CT | C | 6 | a0001c0001t0002g0119a0001c0001t0002g0123a0001c0001t0002g0177others(3): Show | 6 | HG03130.hp2 HG03453.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1652delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599475 | |||||
chr9:105599533
|
ATGTGATC others(23): Show |
A | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-1581_166-1552d others(32): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599533 | |||||
chr9:105599568
|
A | T | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-1577A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599568 | ||||||
chr9:105599661
|
G | A | 2 | a0001c0001t0003g0017a0001c0001t0003g0086 | 3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.166-1484G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599661 | ||||||
chr9:105599689
|
A | C | 1 | a0001c0001t0007g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.166-1456A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599689 | ||||||
chr9:105599712
|
C | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-1433C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599712 | ||||||
chr9:105599790
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.166-1355A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599790 | ||||||
chr9:105599923
|
C | CT | 2 | a0001c0001t0001g0047a0001c0001t0001g0283 | 3 | NA18992.hp2 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.166-1221dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599923 | |||||
chr9:105600008
|
T | C | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.166-1137T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600008 | ||||||
chr9:105600026
|
T | C | 1 | a0002c0002t0008g0008 | 3 | NA18948.hp1 NA18951.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.166-1119T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600026 | ||||||
chr9:105600106
|
C | T | 1 | a0001c0001t0012g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.166-1039C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600106 | ||||||
chr9:105600371
|
A | G | 1 | a0002c0002t0004g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-774A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600371 | ||||||
chr9:105600414
|
A | T | 1 | a0002c0002t0004g0186 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.166-731A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600414 | ||||||
chr9:105600508
|
T | G | 26 | a0002c0002t0001g0270a0002c0002t0001g0272a0002c0002t0001g0278others(23): Show | 28 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-637T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600508 | ||||||
chr9:105600564
|
A | G | 250 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(247): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.166-581A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600564 | ||||||
chr9:105600637
|
A | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-508A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600637 | ||||||
chr9:105600817
|
T | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-328T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600817 | ||||||
chr9:105600853
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.166-292G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600853 | ||||||
chr9:105601041
|
G | A | 1 | a0003c0003t0001g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166-104G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105601041 | ||||||
chr9:105601139
|
A | G | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.166-6A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105601139 | ||||||
chr9:105601391
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.369+43C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601391 | ||||||
chr9:105601434
|
A | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0313 | 2 | NA18979.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.369+86A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601434 | ||||||
chr9:105601453
|
T | C | 1 | a0002c0002t0004g0186 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.369+105T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601453 | ||||||
chr9:105601654
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.369+306C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601654 | ||||||
chr9:105601740
|
C | T | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.369+392C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601740 | ||||||
chr9:105601752
|
G | T | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+404G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601752 | ||||||
chr9:105601813
|
A | T | 13 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(10): Show | 13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.369+465A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601813 | ||||||
chr9:105602173
|
G | A | 2 | a0001c0005t0013g0032a0001c0005t0013g0181 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.369+825G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602173 | ||||||
chr9:105602306
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.369+958G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602306 | ||||||
chr9:105602587
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.369+1239G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602587 | ||||||
chr9:105602633
|
G | T | 1 | a0002c0002t0004g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369+1285G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602633 | ||||||
chr9:105602891
|
T | A | 5 | a0001c0001t0002g0118a0001c0001t0002g0127a0001c0001t0002g0128others(2): Show | 5 | HG00621.hp1 HG02027.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-1324T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602891 | ||||||
chr9:105602918
|
C | A | 6 | a0001c0001t0002g0108a0001c0001t0002g0122a0001c0001t0002g0130others(3): Show | 6 | NA18963.hp1 NA18991.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1297C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602918 | ||||||
chr9:105602944
|
A | G | 1 | a0001c0001t0027g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.370-1271A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602944 | ||||||
chr9:105603180
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.370-1035C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603180 | ||||||
chr9:105603181
|
G | A | 15 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(12): Show | 15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.370-1034G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603181 | ||||||
chr9:105603200
|
C | T | 4 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(1): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-1015C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603200 | ||||||
chr9:105603234
|
A | G | 5 | a0001c0001t0002g0108a0001c0001t0002g0122a0001c0001t0002g0130others(2): Show | 5 | NA18963.hp1 NA18991.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-981A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603234 | ||||||
chr9:105603281
|
G | A | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.370-934G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603281 | ||||||
chr9:105603297
|
G | C | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.370-918G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603297 | ||||||
chr9:105603435
|
T | C | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.370-780T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603435 | ||||||
chr9:105603462
|
T | C | 1 | a0002c0002t0004g0196 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.370-753T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603462 | ||||||
chr9:105603582
|
AT | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-632delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603582 | ||||||
chr9:105603679
|
G | T | 4 | a0001c0001t0006g0221a0001c0001t0006g0223a0001c0001t0018g0222others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-536G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603679 | ||||||
chr9:105603679
|
GT | G | 15 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(12): Show | 15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.370-524delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 105603679 | |||||
chr9:105603799
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.370-416A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603799 | ||||||
chr9:105603902
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.370-313A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603902 | ||||||
chr9:105603954
|
T | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.370-261T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603954 | ||||||
chr9:105604528
|
G | A | 4 | a0001c0001t0006g0221a0001c0001t0006g0223a0001c0001t0018g0222others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+36G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604528 | ||||||
chr9:105604703
|
C | T | 1 | a0007c0012t0004g0213 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.647+211C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604703 | ||||||
chr9:105604812
|
C | T | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+320C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604812 | ||||||
chr9:105604870
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.647+378T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604870 | ||||||
chr9:105604896
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.647+404T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604896 | ||||||
chr9:105604955
|
C | A | 47 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(44): Show | 53 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+463C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604955 | ||||||
chr9:105604955
|
C | CA | 15 | a0001c0001t0001g0292a0001c0001t0001g0307a0001c0001t0002g0022others(12): Show | 16 | HG01261.hp1 HG02165.hp1 HG03098.hp2 others(13): Show |
intron_variant | MODIFIER | c.647+479dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105604955 | |||||
chr9:105605128
|
A | T | 5 | a0001c0001t0002g0140a0001c0001t0012g0059a0001c0001t0012g0060others(2): Show | 5 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+636A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605128 | ||||||
chr9:105605163
|
A | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 5 | HG00099.hp1 HG00280.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+671A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605163 | ||||||
chr9:105605166
|
AAC | A | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+676_647+677del others(2): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105605166 | |||||
chr9:105605225
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.647+733A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605225 | ||||||
chr9:105605416
|
G | A | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.647+924G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605416 | ||||||
chr9:105605692
|
T | A | 1 | a0001c0001t0002g0144 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.647+1200T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605692 | ||||||
chr9:105605882
|
TA | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.647+1394delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105605882 | |||||
chr9:105605990
|
G | A | 47 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(44): Show | 53 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+1498G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605990 | ||||||
chr9:105606070
|
A | T | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0121others(1): Show | 5 | NA18953.hp1 NA18968.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.647+1578A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606070 | ||||||
chr9:105606103
|
A | T | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+1611A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606103 | ||||||
chr9:105606202
|
C | G | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.648-1617C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606202 | ||||||
chr9:105606257
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0257a0001c0001t0001g0313others(4): Show | 7 | NA18949.hp1 NA18957.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.648-1562A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606257 | ||||||
chr9:105606415
|
C | T | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-1404C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606415 | ||||||
chr9:105606481
|
T | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.648-1338T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606481 | ||||||
chr9:105606515
|
A | G | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.648-1304A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606515 | ||||||
chr9:105606541
|
A | C | 2 | a0001c0001t0006g0235a0001c0001t0006g0245 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.648-1278A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606541 | ||||||
chr9:105606673
|
T | G | 6 | a0002c0002t0004g0196a0002c0002t0008g0008a0002c0002t0008g0201others(3): Show | 8 | HG00597.hp1 HG01074.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.648-1146T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606673 | ||||||
chr9:105606680
|
AAT | A | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.648-1126_648-1125d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105606680 | |||||
chr9:105606682
|
T | A | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.648-1137T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606682 | ||||||
chr9:105606694
|
TTA | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1115_648-1114d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105606694 | |||||
chr9:105606702
|
A | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1117A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606702 | ||||||
chr9:105606704
|
A | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1115A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606704 | ||||||
chr9:105606706
|
G | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1113G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606706 | ||||||
chr9:105606707
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1112T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606707 | ||||||
chr9:105606709
|
T | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1110T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606709 | ||||||
chr9:105606709
|
T | TTCTC | 248 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0220others(245): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.648-1106_648-1103d others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105606709 | |||||
chr9:105606779
|
G | A | 47 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(44): Show | 53 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.648-1040G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606779 | ||||||
chr9:105606803
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.648-1016C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606803 | ||||||
chr9:105606816
|
T | G | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.648-1003T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606816 | ||||||
chr9:105606869
|
A | G | 1 | a0001c0001t0001g0034 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.648-950A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606869 | ||||||
chr9:105606950
|
A | G | 1 | a0001c0006t0014g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.648-869A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606950 | ||||||
chr9:105607093
|
G | C | 237 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(234): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.648-726G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607093 | ||||||
chr9:105607338
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-481A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607338 | ||||||
chr9:105607561
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.648-258G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607561 | ||||||
chr9:105607690
|
T | A | 1 | a0001c0001t0001g0298 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.648-129T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607690 | ||||||
chr9:105608023
|
T | C | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.780+72T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608023 | ||||||
chr9:105608063
|
C | G | 1 | a0001c0001t0002g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.780+112C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608063 | ||||||
chr9:105608080
|
T | C | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.780+129T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608080 | ||||||
chr9:105608102
|
T | G | 2 | a0002c0002t0004g0188a0002c0002t0025g0200 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.780+151T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608102 | ||||||
chr9:105608117
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.780+166A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608117 | ||||||
chr9:105608244
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.780+293T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608244 | ||||||
chr9:105608264
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0220 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.780+313C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608264 | ||||||
chr9:105608301
|
C | G | 1 | a0001c0013t0002g0311 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.780+350C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608301 | ||||||
chr9:105608393
|
G | T | 1 | a0003c0003t0001g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.780+442G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608393 | ||||||
chr9:105608638
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0177 | 2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.780+687C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608638 | ||||||
chr9:105608689
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+738G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608689 | ||||||
chr9:105608778
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+827C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608778 | ||||||
chr9:105608857
|
CAT | C | 16 | a0001c0001t0006g0014a0001c0001t0006g0037a0001c0001t0006g0052others(13): Show | 19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+907_780+908del others(2): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608857 | ||||||
chr9:105609040
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+1089C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609040 | ||||||
chr9:105609056
|
A | G | 8 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0019others(5): Show | 11 | HG00323.hp1 HG00741.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+1105A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609056 | ||||||
chr9:105609217
|
G | A | 1 | a0002c0002t0004g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.780+1266G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609217 | ||||||
chr9:105609217
|
G | T | 2 | a0002c0002t0001g0288a0002c0002t0001g0290 | 2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.780+1266G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609217 | ||||||
chr9:105609230
|
T | G | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.780+1279T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609230 | ||||||
chr9:105609268
|
C | T | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.780+1317C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609268 | ||||||
chr9:105609338
|
G | A | 1 | a0001c0001t0002g0028 | 2 | HG02523.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.780+1387G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609338 | ||||||
chr9:105609353
|
T | C | 5 | a0001c0001t0001g0107a0001c0001t0002g0024a0001c0001t0002g0131others(2): Show | 6 | HG02148.hp1 HG02273.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+1402T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609353 | ||||||
chr9:105609509
|
C | T | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(44): Show | 60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.780+1558C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609509 | ||||||
chr9:105609535
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.780+1584A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609535 | ||||||
chr9:105609646
|
T | A | 1 | a0001c0005t0026g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.780+1695T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609646 | ||||||
chr9:105609758
|
AT | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+1809delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105609758 | |||||
chr9:105609843
|
G | A | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+1892G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609843 | ||||||
chr9:105610003
|
T | C | 13 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(10): Show | 13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.780+2052T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610003 | ||||||
chr9:105610075
|
A | G | 2 | a0002c0002t0001g0279a0002c0002t0001g0294 | 2 | HG02004.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.780+2124A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610075 | ||||||
chr9:105610755
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+2804C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610755 | ||||||
chr9:105610757
|
T | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.780+2806T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610757 | ||||||
chr9:105610773
|
G | A | 317 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(314): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.780+2822G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610773 | ||||||
chr9:105610854
|
C | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.780+2903C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610854 | ||||||
chr9:105610903
|
C | A | 97 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(94): Show | 108 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.780+2952C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610903 | ||||||
chr9:105610980
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3029C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610980 | ||||||
chr9:105611063
|
A | G | 2 | a0004c0004t0005g0039a0004c0004t0005g0253 | 3 | HG00140.hp1 HG00735.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.780+3112A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611063 | ||||||
chr9:105611223
|
C | T | 5 | a0002c0002t0001g0272a0002c0002t0001g0287a0002c0002t0001g0288others(2): Show | 5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+3272C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611223 | ||||||
chr9:105611328
|
A | T | 16 | a0001c0001t0006g0014a0001c0001t0006g0037a0001c0001t0006g0052others(13): Show | 19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+3377A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611328 | ||||||
chr9:105611500
|
C | A | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3549C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611500 | ||||||
chr9:105611601
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0220 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.780+3650G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611601 | ||||||
chr9:105611704
|
C | T | 4 | a0001c0001t0005g0237a0001c0001t0005g0248a0001c0001t0005g0249others(1): Show | 4 | HG00280.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-3574C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611704 | ||||||
chr9:105611817
|
G | A | 1 | a0001c0001t0006g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.781-3461G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611817 | ||||||
chr9:105611935
|
C | T | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.781-3343C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611935 | ||||||
chr9:105612015
|
G | GTTTAT | 5 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(2): Show | 5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-3236_781-3232d others(7): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105612015 | |||||
chr9:105612241
|
A | T | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.781-3037A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612241 | ||||||
chr9:105612357
|
T | C | 4 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0267others(1): Show | 4 | NA18970.hp1 NA18977.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-2921T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612357 | ||||||
chr9:105612503
|
G | GT | 238 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(235): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.781-2771dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105612503 | |||||
chr9:105612556
|
A | T | 1 | a0001c0008t0003g0095 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.781-2722A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612556 | ||||||
chr9:105612690
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.781-2588C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612690 | ||||||
chr9:105613080
|
T | C | 12 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(9): Show | 12 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-2198T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613080 | ||||||
chr9:105613113
|
T | C | 1 | a0002c0002t0025g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781-2165T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613113 | ||||||
chr9:105613195
|
T | A | 3 | a0001c0001t0002g0120a0001c0001t0002g0133a0001c0001t0002g0146 | 3 | HG00408.hp1 HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.781-2083T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613195 | ||||||
chr9:105613352
|
T | C | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.781-1926T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613352 | ||||||
chr9:105613424
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1854G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613424 | ||||||
chr9:105613465
|
A | G | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.781-1813A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613465 | ||||||
chr9:105613577
|
G | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1701G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613577 | ||||||
chr9:105613755
|
T | C | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-1523T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613755 | ||||||
chr9:105613829
|
A | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-1449A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613829 | ||||||
chr9:105613980
|
G | A | 4 | a0002c0002t0004g0031a0002c0002t0004g0195a0002c0002t0004g0197others(1): Show | 5 | HG02559.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-1298G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613980 | ||||||
chr9:105614103
|
A | AC | 3 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0303 | 5 | HG00639.hp1 HG00642.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-1173dupC | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105614103 | |||||
chr9:105614155
|
A | G | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.781-1123A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614155 | ||||||
chr9:105614366
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-912A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614366 | ||||||
chr9:105614383
|
TTTCA | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-886_781-883del others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105614383 | |||||
chr9:105614480
|
T | C | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.781-798T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614480 | ||||||
chr9:105614600
|
T | A | 1 | a0002c0002t0004g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.781-678T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614600 | ||||||
chr9:105614816
|
G | A | 62 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(59): Show | 68 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.781-462G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614816 | ||||||
chr9:105614884
|
C | CT | 51 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(48): Show | 64 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.781-382dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105614884 | |||||
chr9:105614888
|
T | C | 1 | a0002c0002t0004g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781-390T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614888 | ||||||
chr9:105614976
|
C | T | 1 | a0002c0002t0001g0290 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.781-302C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614976 | ||||||
chr9:105615015
|
C | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-263C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105615015 | ||||||
chr9:105615025
|
AG | A | 93 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.781-251delG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105615025 | |||||
chr9:105615055
|
T | TA | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-222dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105615055 | |||||
chr9:105615115
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.781-163C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105615115 | ||||||
chr9:105615421
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.910+14G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615421 | ||||||
chr9:105615452
|
C | T | 2 | a0001c0001t0003g0017a0001c0001t0003g0086 | 3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.910+45C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615452 | ||||||
chr9:105615466
|
A | G | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.910+59A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615466 | ||||||
chr9:105615697
|
T | G | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.910+290T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615697 | ||||||
chr9:105615740
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+333C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615740 | ||||||
chr9:105615743
|
T | C | 49 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0019g0190others(46): Show | 55 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.910+336T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615743 | ||||||
chr9:105615762
|
C | T | 44 | a0002c0002t0001g0270a0002c0002t0001g0272a0002c0002t0001g0278others(41): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.910+355C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615762 | ||||||
chr9:105615770
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0110 | 2 | NA18747.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.910+363T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615770 | ||||||
chr9:105615832
|
A | G | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+425A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615832 | ||||||
chr9:105615918
|
A | T | 1 | a0003c0003t0001g0239 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.910+511A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615918 | ||||||
chr9:105616145
|
C | A | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+738C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616145 | ||||||
chr9:105616190
|
G | T | 8 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+783G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616190 | ||||||
chr9:105616236
|
A | G | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+829A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616236 | ||||||
chr9:105616605
|
CTTGA | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+1201_910+1204d others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 105616605 | |||||
chr9:105616660
|
A | G | 4 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(1): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+1253A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616660 | ||||||
chr9:105616861
|
C | G | 1 | a0001c0001t0001g0045 | 2 | NA19001.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.911-1098C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616861 | ||||||
chr9:105616879
|
C | CA | 52 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0281others(49): Show | 60 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.911-1065dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 105616879 | |||||
chr9:105616881
|
A | G | 4 | a0001c0001t0006g0221a0001c0001t0006g0223a0001c0001t0018g0222others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-1078A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616881 | ||||||
chr9:105617107
|
A | G | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.911-852A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617107 | ||||||
chr9:105617316
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.911-643T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617316 | ||||||
chr9:105617547
|
C | T | 1 | a0001c0001t0002g0143 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.911-412C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617547 | ||||||
chr9:105617673
|
TCAAA | T | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.911-281_911-278del others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 105617673 | |||||
chr9:105617699
|
T | C | 1 | a0001c0001t0002g0127 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.911-260T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617699 | ||||||
chr9:105617723
|
G | A | 158 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(155): Show | 175 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.911-236G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617723 | ||||||
chr9:105618136
|
A | G | 1 | a0002c0002t0004g0194 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1044+44A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618136 | ||||||
chr9:105618150
|
C | T | 15 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(12): Show | 15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1044+58C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618150 | ||||||
chr9:105618176
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1044+84A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618176 | ||||||
chr9:105618241
|
A | T | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1044+149A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618241 | ||||||
chr9:105618440
|
A | G | 48 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0019g0190others(45): Show | 54 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1044+348A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618440 | ||||||
chr9:105618464
|
C | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0220 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1044+372C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618464 | ||||||
chr9:105618465
|
C | T | 1 | a0001c0013t0002g0311 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1044+373C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618465 | ||||||
chr9:105618508
|
G | A | 2 | a0001c0006t0014g0048a0001c0006t0014g0049 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1044+416G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618508 | ||||||
chr9:105618761
|
T | C | 2 | a0001c0001t0003g0017a0001c0001t0003g0086 | 3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1044+669T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618761 | ||||||
chr9:105618848
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1044+756T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618848 | ||||||
chr9:105618916
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1044+824G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618916 | ||||||
chr9:105619053
|
C | T | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-881C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619053 | ||||||
chr9:105619058
|
T | TA | 6 | a0001c0001t0001g0107a0001c0001t0002g0122a0001c0001t0002g0134others(3): Show | 6 | HG03098.hp2 HG03130.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-859dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 105619058 | |||||
chr9:105619058
|
TA | T | 51 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0002g0143others(48): Show | 57 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1045-859delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 105619058 | |||||
chr9:105619156
|
G | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-778G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619156 | ||||||
chr9:105619482
|
G | T | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1045-452G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619482 | ||||||
chr9:105619639
|
G | C | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1045-295G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619639 | ||||||
chr9:105619744
|
T | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1045-190T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619744 | ||||||
chr9:105619894
|
C | A | 1 | a0001c0001t0006g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1045-40C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619894 | ||||||
chr9:105620147
|
C | A | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1172+86C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105620147 | ||||||
chr9:105620659
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1172+598A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105620659 | ||||||
chr9:105620711
|
C | G | 1 | a0001c0001t0003g0102 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1172+650C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105620711 | ||||||
chr9:105620775
|
A | ATAG | 44 | a0001c0001t0001g0011a0001c0001t0002g0026a0001c0001t0002g0106others(41): Show | 52 | HG00099.hp2 HG00323.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1172+759_1172+761d others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | |||||
chr9:105620775
|
A | ATAGTAG | 86 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0220others(83): Show | 99 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1172+756_1172+761d others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | |||||
chr9:105620775
|
A | ATAGTAGT others(2): Show |
35 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0066others(32): Show | 38 | HG00408.hp1 HG00558.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1172+753_1172+761d others(11): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | |||||
chr9:105620775
|
A | ATAGTAGT others(5): Show |
11 | a0001c0001t0002g0111a0001c0001t0002g0143a0001c0001t0002g0149others(8): Show | 11 | HG00140.hp2 HG01074.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1172+750_1172+761d others(14): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | |||||
chr9:105620775
|
A | ATAGTAGT others(8): Show |
1 | a0001c0001t0002g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1172+747_1172+761d others(17): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | |||||
chr9:105620775
|
ATAG | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(100): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1172+759_1172+761d others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | |||||
chr9:105620775
|
ATAGTAG | A | 7 | a0001c0001t0001g0310a0001c0001t0003g0069a0001c0001t0003g0096others(4): Show | 8 | HG01099.hp2 HG01192.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1172+756_1172+761d others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | |||||
chr9:105621124
|
C | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+1063C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621124 | ||||||
chr9:105621147
|
G | A | 98 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(95): Show | 109 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1172+1086G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621147 | ||||||
chr9:105621517
|
T | A | 238 | a0001c0001t0001g0107a0001c0001t0001g0256a0001c0001t0002g0003others(235): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1172+1456T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621517 | ||||||
chr9:105621522
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0041 | 5 | NA18967.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.1172+1461T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621522 | ||||||
chr9:105621682
|
C | T | 91 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(88): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1172+1621C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621682 | ||||||
chr9:105621793
|
A | G | 98 | a0001c0001t0001g0107a0001c0001t0002g0003a0001c0001t0002g0007others(95): Show | 109 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1172+1732A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621793 | ||||||
chr9:105621911
|
G | A | 2 | a0001c0001t0017g0018a0001c0001t0048g0088 | 3 | HG02071.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1172+1850G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621911 | ||||||
chr9:105622204
|
C | A | 1 | a0001c0001t0027g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1172+2143C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622204 | ||||||
chr9:105622222
|
G | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172+2161G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622222 | ||||||
chr9:105622515
|
T | G | 1 | a0001c0005t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1172+2454T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622515 | ||||||
chr9:105622901
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+2840G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622901 | ||||||
chr9:105622910
|
A | G | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1172+2849A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622910 | ||||||
chr9:105622923
|
G | A | 48 | a0001c0001t0001g0256a0001c0001t0003g0001a0001c0001t0003g0005others(45): Show | 61 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1172+2862G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622923 | ||||||
chr9:105622941
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0308 | 5 | NA18942.hp2 NA19001.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1172+2880C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622941 | ||||||
chr9:105622956
|
G | A | 48 | a0001c0001t0001g0256a0001c0001t0003g0001a0001c0001t0003g0005others(45): Show | 61 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1172+2895G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622956 | ||||||
chr9:105623150
|
G | T | 2 | a0002c0002t0022g0203a0002c0002t0023g0204 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1172+3089G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623150 | ||||||
chr9:105623194
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+3133G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623194 | ||||||
chr9:105623248
|
ATACT | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172+3192_1172+319 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105623248 | |||||
chr9:105623442
|
A | C | 1 | a0002c0002t0001g0294 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1172+3381A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623442 | ||||||
chr9:105623645
|
G | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+3584G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623645 | ||||||
chr9:105623790
|
C | T | 6 | a0001c0001t0002g0108a0001c0001t0002g0122a0001c0001t0002g0130others(3): Show | 6 | NA18963.hp1 NA18991.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1172+3729C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623790 | ||||||
chr9:105624075
|
A | G | 11 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 13 | HG00673.hp1 NA18942.hp2 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.1172+4014A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624075 | ||||||
chr9:105624096
|
T | C | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1172+4035T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624096 | ||||||
chr9:105624400
|
A | G | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1172+4339A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624400 | ||||||
chr9:105624417
|
C | T | 1 | a0001c0001t0006g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1172+4356C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624417 | ||||||
chr9:105624452
|
C | T | 1 | a0002c0002t0004g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1172+4391C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624452 | ||||||
chr9:105624515
|
C | T | 7 | a0001c0001t0002g0105a0001c0001t0002g0138a0001c0001t0002g0139others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1172+4454C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624515 | ||||||
chr9:105624599
|
C | T | 4 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(1): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1172+4538C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624599 | ||||||
chr9:105624623
|
C | CA | 12 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0283others(9): Show | 14 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.1172+4580dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105624623 | |||||
chr9:105624623
|
CA | C | 6 | a0001c0001t0001g0301a0001c0001t0002g0123a0001c0001t0002g0143others(3): Show | 7 | HG01975.hp1 HG02735.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1172+4580delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105624623 | |||||
chr9:105624640
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1172+4579A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624640 | ||||||
chr9:105624894
|
T | C | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+4833T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624894 | ||||||
chr9:105624966
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1172+4905C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624966 | ||||||
chr9:105625100
|
T | C | 8 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1172+5039T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105625100 | ||||||
chr9:105625836
|
TA | T | 9 | a0003c0003t0001g0225a0003c0003t0001g0226a0003c0003t0001g0227others(6): Show | 9 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1172+5787delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105625836 | |||||
chr9:105625923
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1172+5862C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105625923 | ||||||
chr9:105626048
|
T | C | 1 | a0001c0001t0016g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1172+5987T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626048 | ||||||
chr9:105626113
|
T | C | 2 | a0001c0005t0013g0032a0001c0005t0013g0181 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1172+6052T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626113 | ||||||
chr9:105626166
|
G | A | 2 | a0001c0006t0014g0048a0001c0006t0014g0049 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1172+6105G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626166 | ||||||
chr9:105626180
|
A | G | 1 | a0001c0001t0003g0021 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1172+6119A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626180 | ||||||
chr9:105626356
|
C | T | 2 | a0001c0001t0009g0282a0001c0001t0009g0309 | 2 | NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1172+6295C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626356 | ||||||
chr9:105626423
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1172+6362G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626423 | ||||||
chr9:105626627
|
T | C | 1 | a0001c0001t0016g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1172+6566T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626627 | ||||||
chr9:105626698
|
C | T | 89 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(86): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1172+6637C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626698 | ||||||
chr9:105626971
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0297 | 2 | NA18983.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1172+6910C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626971 | ||||||
chr9:105626981
|
C | CTTTTTTT | 8 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(5): Show | 8 | HG01255.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1172+6930_1172+693 others(11): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105626981 | |||||
chr9:105626981
|
CT | C | 203 | a0001c0001t0001g0254a0001c0001t0001g0260a0001c0001t0002g0003others(200): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1172+6936delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105626981 | |||||
chr9:105627220
|
C | A | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1172+7159C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627220 | ||||||
chr9:105627625
|
A | G | 9 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(6): Show | 9 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173-7426A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627625 | ||||||
chr9:105627722
|
T | G | 1 | a0003c0003t0001g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1173-7329T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627722 | ||||||
chr9:105627934
|
C | A | 1 | a0002c0002t0008g0201 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1173-7117C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627934 | ||||||
chr9:105627972
|
A | G | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-7079A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627972 | ||||||
chr9:105627979
|
A | G | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-7072A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627979 | ||||||
chr9:105628090
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1173-6961T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628090 | ||||||
chr9:105628252
|
G | T | 4 | a0001c0001t0003g0016a0001c0001t0003g0019a0001c0001t0003g0080others(1): Show | 6 | HG00741.hp1 HG01099.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173-6799G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628252 | ||||||
chr9:105628311
|
G | T | 15 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(12): Show | 15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1173-6740G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628311 | ||||||
chr9:105628323
|
C | T | 3 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182 | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173-6728C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628323 | ||||||
chr9:105628419
|
T | C | 1 | a0002c0002t0004g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1173-6632T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628419 | ||||||
chr9:105628448
|
A | AG | 30 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1173-6602dupG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105628448 | |||||
chr9:105628615
|
A | G | 2 | a0001c0005t0013g0032a0001c0005t0013g0181 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1173-6436A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628615 | ||||||
chr9:105628645
|
C | A | 1 | a0001c0001t0002g0178 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1173-6406C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628645 | ||||||
chr9:105628663
|
C | T | 4 | a0001c0001t0011g0205a0001c0001t0011g0206a0001c0001t0011g0209others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-6388C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628663 | ||||||
chr9:105628846
|
G | A | 4 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173-6205G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628846 | ||||||
chr9:105629028
|
TAAGA | T | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-6022_1173-601 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629028 | ||||||
chr9:105629056
|
C | G | 14 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1173-5995C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629056 | ||||||
chr9:105629084
|
A | T | 1 | a0001c0001t0002g0119 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-5967A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629084 | ||||||
chr9:105629130
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1173-5921G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629130 | ||||||
chr9:105629179
|
T | C | 1 | a0001c0001t0002g0131 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1173-5872T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629179 | ||||||
chr9:105629184
|
A | G | 2 | a0002c0002t0004g0029a0002c0002t0004g0030 | 4 | HG00099.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5867A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629184 | ||||||
chr9:105629218
|
T | C | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5833T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629218 | ||||||
chr9:105629287
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1173-5764G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629287 | ||||||
chr9:105629292
|
C | G | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173-5759C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629292 | ||||||
chr9:105629295
|
A | G | 4 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0012g0061others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5756A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629295 | ||||||
chr9:105629311
|
A | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5740A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629311 | ||||||
chr9:105629425
|
G | C | 1 | a0001c0001t0002g0119 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-5626G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629425 | ||||||
chr9:105629456
|
A | T | 1 | a0001c0001t0002g0119 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-5595A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629456 | ||||||
chr9:105629581
|
G | C | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5470G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629581 | ||||||
chr9:105629704
|
G | A | 236 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(233): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1173-5347G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629704 | ||||||
chr9:105629934
|
A | G | 101 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(98): Show | 112 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1173-5117A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629934 | ||||||
chr9:105630042
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1173-5009G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630042 | ||||||
chr9:105630165
|
C | T | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-4886C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630165 | ||||||
chr9:105630201
|
TA | T | 9 | a0001c0001t0002g0119a0001c0001t0003g0068a0001c0001t0003g0069others(6): Show | 9 | HG00673.hp2 HG03927.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173-4842delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105630201 | |||||
chr9:105630280
|
A | C | 1 | a0001c0001t0002g0119 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-4771A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630280 | ||||||
chr9:105630326
|
A | T | 1 | a0001c0001t0002g0119 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-4725A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630326 | ||||||
chr9:105630403
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1173-4648C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630403 | ||||||
chr9:105630424
|
C | T | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1173-4627C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630424 | ||||||
chr9:105630455
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1173-4596C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630455 | ||||||
chr9:105630543
|
A | C | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1173-4508A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630543 | ||||||
chr9:105630548
|
A | T | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1173-4503A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630548 | ||||||
chr9:105630624
|
T | G | 1 | a0001c0001t0027g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1173-4427T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630624 | ||||||
chr9:105630807
|
A | G | 1 | a0001c0001t0012g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1173-4244A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630807 | ||||||
chr9:105631061
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1173-3990A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631061 | ||||||
chr9:105631191
|
C | T | 1 | a0002c0002t0022g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1173-3860C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631191 | ||||||
chr9:105631505
|
T | C | 319 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(316): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1173-3546T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631505 | ||||||
chr9:105631540
|
C | G | 1 | a0002c0002t0004g0031 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1173-3511C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631540 | ||||||
chr9:105631622
|
C | A | 13 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(10): Show | 14 | HG00673.hp2 HG02071.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1173-3429C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631622 | ||||||
chr9:105631779
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1173-3272A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631779 | ||||||
chr9:105631883
|
G | A | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1173-3168G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631883 | ||||||
chr9:105631904
|
C | G | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-3147C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631904 | ||||||
chr9:105631967
|
C | A | 8 | a0001c0001t0006g0014a0001c0001t0006g0037a0001c0001t0006g0052others(5): Show | 11 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1173-3084C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631967 | ||||||
chr9:105631969
|
G | A | 12 | a0001c0001t0006g0014a0001c0001t0006g0037a0001c0001t0006g0052others(9): Show | 15 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173-3082G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631969 | ||||||
chr9:105632082
|
G | C | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1173-2969G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632082 | ||||||
chr9:105632157
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA18969.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1173-2894C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632157 | ||||||
chr9:105632185
|
G | A | 1 | a0001c0001t0012g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1173-2866G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632185 | ||||||
chr9:105632187
|
A | G | 48 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(45): Show | 61 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1173-2864A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632187 | ||||||
chr9:105632233
|
A | C | 48 | a0001c0005t0013g0032a0001c0005t0013g0181a0001c0005t0026g0182others(45): Show | 54 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1173-2818A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632233 | ||||||
chr9:105632294
|
G | C | 1 | a0001c0001t0010g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1173-2757G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632294 | ||||||
chr9:105632419
|
T | TA | 65 | a0001c0001t0005g0036a0001c0001t0005g0237a0001c0001t0005g0248others(62): Show | 76 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1173-2623dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105632419 | |||||
chr9:105632425
|
A | T | 1 | a0001c0001t0012g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1173-2626A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632425 | ||||||
chr9:105632427
|
A | AT | 9 | a0001c0001t0040g0250a0002c0002t0001g0270a0002c0002t0004g0188others(6): Show | 12 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173-2624_1173-262 others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632427 | ||||||
chr9:105632427
|
A | T | 31 | a0001c0001t0002g0154a0001c0001t0010g0053a0001c0001t0010g0054others(28): Show | 31 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1173-2624A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632427 | ||||||
chr9:105632429
|
T | A | 46 | a0001c0001t0001g0273a0001c0001t0001g0291a0001c0001t0003g0001others(43): Show | 59 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1173-2622T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632429 | ||||||
chr9:105632438
|
AT | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-2612delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632438 | ||||||
chr9:105632440
|
AT | A | 10 | a0001c0001t0010g0053a0001c0001t0010g0054a0001c0001t0010g0055others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173-2610delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632440 | ||||||
chr9:105632441
|
T | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-2610T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632441 | ||||||
chr9:105632577
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1173-2474G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632577 | ||||||
chr9:105632612
|
A | G | 44 | a0002c0002t0001g0270a0002c0002t0001g0272a0002c0002t0001g0278others(41): Show | 49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1173-2439A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632612 | ||||||
chr9:105632616
|
G | A | 4 | a0001c0006t0014g0048a0001c0006t0014g0049a0001c0006t0015g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-2435G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632616 | ||||||
chr9:105632656
|
T | G | 1 | a0006c0010t0041g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173-2395T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632656 | ||||||
chr9:105632747
|
A | G | 1 | a0001c0001t0006g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1173-2304A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632747 | ||||||
chr9:105632799
|
T | C | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1173-2252T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632799 | ||||||
chr9:105632914
|
A | G | 317 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(314): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1173-2137A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632914 | ||||||
chr9:105633651
|
A | G | 249 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(246): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1173-1400A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105633651 | ||||||
chr9:105633753
|
G | A | 89 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(86): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1173-1298G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105633753 | ||||||
chr9:105633770
|
G | A | 2 | a0001c0001t0046g0057a0006c0010t0041g0058 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1173-1281G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105633770 | ||||||
chr9:105634282
|
C | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(90): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1173-769C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634282 | ||||||
chr9:105634353
|
C | T | 103 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(100): Show | 114 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1173-698C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634353 | ||||||
chr9:105634635
|
C | G | 1 | a0009c0014t0043g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1173-416C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634635 | ||||||
chr9:105634735
|
C | T | 89 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0022others(86): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1173-316C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634735 | ||||||
chr9:105634737
|
A | G | 1 | a0001c0006t0014g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1173-314A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634737 | ||||||
chr9:105634824
|
T | C | 1 | a0001c0001t0003g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1173-227T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634824 | ||||||
chr9:105634891
|
A | G | 1 | a0001c0001t0046g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1173-160A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634891 |