geneid | 2342 |
---|---|
ensemblid | ENSG00000257365.8 |
hgncid | 3785 |
symbol | FNTB |
name | farnesyltransferase, CAAX box, beta |
refseq_nuc | NM_002028.4 |
refseq_prot | NP_002019.1 |
ensembl_nuc | ENST00000246166.3 |
ensembl_prot | ENSP00000246166.2 |
mane_status | MANE Select |
chr | chr14 |
start | 64986895 |
end | 65062650 |
strand | + |
ver | v1.2 |
region | chr14:64986895-65062650 |
region5000 | chr14:64981895-65067650 |
regionname0 | FNTB_chr14_64986895_65062650 |
regionname5000 | FNTB_chr14_64981895_65067650 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 437 | 357 | 86 | 66 | 153 | 10 | 40 | 110 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0002 | 0/0 | 437 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0003 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0004 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
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 | 1/1 | 1314 | 355 | 86 | 66 | 152 | 10 | 39 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
c0002 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
c0003 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
c0004 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
c0005 | 0/0 | 1314 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
c0006 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
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 | 1/1 | 1398 | 242 | 31 | 52 | 120 | 8 | 29 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
t0002 | 0/0 | 1398 | 113 | 57 | 13 | 33 | 1 | 9 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
t0003 | 0/0 | 1398 | 2 | 0 | 0 | 0 | 0 | 2 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
t0004 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
t0005 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
t0006 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
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 | 2 | 2 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
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 | 1/1 | 1314 | 355 | 86 | 66 | 152 | 10 | 39 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0004 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0005 | 0/0 | 1314 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0002c0006 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0003c0003 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0004c0002 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2711 | 239 | 30 | 52 | 118 | 8 | 29 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0001t0002 | 0/0 | 2711 | 111 | 56 | 13 | 33 | 1 | 8 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0001t0003 | 0/0 | 2711 | 2 | 0 | 0 | 0 | 0 | 2 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0001t0004 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0001t0005 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0001t0006 | 0/0 | 2711 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0004t0001 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0001c0005t0002 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0002c0006t0001 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0003c0003t0001 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
a0004c0002t0002 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | copy fasta | chr14 | 64981895 | 65067650 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0001c0005t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0002c0006t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0003c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
a0004c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | GBR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | FIN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0110 | EUR | IBS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02080 | hp2 | a0002 | c0006 | t0001 | g0213 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0350 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0155 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02602 | hp2 | a0001 | c0005 | t0002 | g0286 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0344 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0105 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ASW | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0042 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | GIH | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | GIH | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0338 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA20300 | hp2 | a0004 | c0002 | t0002 | g0012 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0164 | REF | REF | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0146 | REF | REF | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:65027539
|
A | T | 1 | a0002 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.461A>T | p.Tyr154Phe | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 5/12 | 520/2711 | 461/1314 | 154/437 | chr14 | 65027539 | ||
chr14:65054660
|
G | T | 1 | a0003 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1153G>T | p.Val385Leu | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/12 | 1212/2711 | 1153/1314 | 385/437 | chr14 | 65054660 | ||
chr14:65061259
|
C | T | 1 | a0004 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1261C>T | p.Pro421Ser | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 1320/2711 | 1261/1314 | 421/437 | chr14 | 65061259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:65053323
|
G | T | 1 | a0001c0005 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.1041G>T | p.Ala347Ala | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/12 | 1100/2711 | 1041/1314 | 347/437 | chr14 | 65053323 | ||
chr14:65054635
|
C | T | 1 | a0001c0004 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1128C>T | p.Phe376Phe | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/12 | 1187/2711 | 1128/1314 | 376/437 | chr14 | 65054635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:65061542
|
C | T | 1 | a0001c0001t0006 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 230 | chr14 | 65061542 | |||||
chr14:65061671
|
C | T | 1 | a0001c0001t0005 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*359C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 359 | chr14 | 65061671 | |||||
chr14:65062104
|
C | T | 1 | a0001c0001t0004 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 792 | chr14 | 65062104 | |||||
chr14:65062169
|
A | T | 3 | a0001c0001t0002a0001c0005t0002a0004c0002t0002 | 113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*857A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 857 | chr14 | 65062169 | |||||
chr14:65062174
|
T | C | 3 | a0001c0001t0002a0001c0005t0002a0004c0002t0002 | 113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*862T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 862 | chr14 | 65062174 | |||||
chr14:65062600
|
C | T | 1 | a0001c0001t0003 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1288C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 1288 | chr14 | 65062600 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:64987138
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.144+41T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987138 | ||||||
chr14:64987465
|
T | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(2): Show | 5 | HG01081.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+368T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987465 | ||||||
chr14:64987617
|
C | G | 6 | a0001c0001t0001g0352a0001c0001t0001g0353a0001c0001t0001g0354others(3): Show | 6 | HG02074.hp2 HG02083.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+520C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987617 | ||||||
chr14:64987681
|
C | G | 63 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(60): Show | 64 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.144+584C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987681 | ||||||
chr14:64987997
|
T | G | 1 | a0001c0001t0002g0011 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.144+900T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987997 | ||||||
chr14:64988302
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0007 | 2 | HG01081.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.144+1205G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988302 | ||||||
chr14:64988368
|
T | C | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+1271T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988368 | ||||||
chr14:64988443
|
C | CT | 20 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0281others(17): Show | 20 | HG01192.hp1 HG01934.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.144+1367dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64988443 | |||||
chr14:64988443
|
CT | C | 90 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 91 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.144+1367delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64988443 | |||||
chr14:64988477
|
C | T | 1 | a0001c0001t0001g0342 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.144+1380C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988477 | ||||||
chr14:64988477
|
CG | C | 4 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+1381delG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988477 | ||||||
chr14:64988530
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.144+1433G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988530 | ||||||
chr14:64988585
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG01192.hp1 HG02273.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+1488C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988585 | ||||||
chr14:64988684
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+1587G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988684 | ||||||
chr14:64988733
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.144+1636G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988733 | ||||||
chr14:64988914
|
G | A | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+1817G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988914 | ||||||
chr14:64988949
|
T | C | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.144+1852T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988949 | ||||||
chr14:64988974
|
C | A | 1 | a0001c0001t0002g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.144+1877C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988974 | ||||||
chr14:64989272
|
C | CA | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 40 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.144+2197dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64989272 | |||||
chr14:64989304
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.144+2207C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989304 | ||||||
chr14:64989305
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.144+2208G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989305 | ||||||
chr14:64989313
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.144+2216A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989313 | ||||||
chr14:64989490
|
AGCAAGAC others(4): Show |
A | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+2394_144+2404d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989490 | ||||||
chr14:64989503
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+2406G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989503 | ||||||
chr14:64989521
|
C | G | 75 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(72): Show | 76 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.144+2424C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989521 | ||||||
chr14:64989531
|
T | TA | 75 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(72): Show | 76 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.144+2445dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64989531 | |||||
chr14:64989539
|
AAAAC | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(17): Show | 20 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.144+2450_144+2453d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64989539 | |||||
chr14:64989877
|
A | T | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.144+2780A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989877 | ||||||
chr14:64990090
|
C | A | 1 | a0001c0001t0002g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144+2993C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990090 | ||||||
chr14:64990095
|
G | A | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+2998G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990095 | ||||||
chr14:64990338
|
G | A | 1 | a0001c0001t0002g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.144+3241G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990338 | ||||||
chr14:64990347
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.144+3250A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990347 | ||||||
chr14:64990576
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.144+3479G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990576 | ||||||
chr14:64991019
|
G | C | 3 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0294 | 3 | HG02615.hp2 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.144+3922G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991019 | ||||||
chr14:64991175
|
ATGGCATG others(15): Show |
A | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+4088_144+4109d others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64991175 | |||||
chr14:64991323
|
C | G | 1 | a0001c0001t0001g0272 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.144+4226C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991323 | ||||||
chr14:64991464
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.144+4367C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991464 | ||||||
chr14:64991535
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.144+4438C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991535 | ||||||
chr14:64991553
|
G | A | 12 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 12 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.144+4456G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991553 | ||||||
chr14:64991636
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.144+4539G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991636 | ||||||
chr14:64991704
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.144+4607G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991704 | ||||||
chr14:64991753
|
G | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.144+4656G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991753 | ||||||
chr14:64991773
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.144+4676G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991773 | ||||||
chr14:64991833
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.144+4736G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991833 | ||||||
chr14:64992058
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.144+4961G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992058 | ||||||
chr14:64992207
|
A | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0083others(48): Show | 52 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.144+5110A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992207 | ||||||
chr14:64992241
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+5144A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992241 | ||||||
chr14:64992413
|
T | A | 2 | a0001c0001t0001g0274a0001c0001t0002g0094 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.144+5316T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992413 | ||||||
chr14:64992509
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.144+5412A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992509 | ||||||
chr14:64992720
|
C | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+5623C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992720 | ||||||
chr14:64992724
|
G | C | 1 | a0001c0001t0002g0344 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.144+5627G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992724 | ||||||
chr14:64992776
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.144+5679G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992776 | ||||||
chr14:64992906
|
A | G | 1 | a0001c0001t0002g0227 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.144+5809A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992906 | ||||||
chr14:64992982
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.144+5885T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992982 | ||||||
chr14:64993028
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.144+5931G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993028 | ||||||
chr14:64993071
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0002g0094 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.144+5974C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993071 | ||||||
chr14:64993111
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0002g0094 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.144+6014C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993111 | ||||||
chr14:64993133
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.144+6036A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993133 | ||||||
chr14:64993341
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.144+6244A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993341 | ||||||
chr14:64993421
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0097 | 2 | NA18942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.144+6324G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993421 | ||||||
chr14:64993442
|
C | T | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+6345C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993442 | ||||||
chr14:64993454
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.144+6357G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993454 | ||||||
chr14:64993512
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+6415A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993512 | ||||||
chr14:64993632
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+6535G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993632 | ||||||
chr14:64993707
|
C | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+6610C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993707 | ||||||
chr14:64993722
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.144+6625G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993722 | ||||||
chr14:64993838
|
C | CT | 28 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 29 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.144+6752dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64993838 | |||||
chr14:64993858
|
A | C | 37 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0092others(34): Show | 37 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.144+6761A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993858 | ||||||
chr14:64993933
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0340 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.144+6836G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993933 | ||||||
chr14:64994135
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+7038G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994135 | ||||||
chr14:64994194
|
G | T | 7 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0002g0035others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.144+7097G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994194 | ||||||
chr14:64994226
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.144+7129C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994226 | ||||||
chr14:64994283
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0197 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.144+7186C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994283 | ||||||
chr14:64994655
|
A | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.144+7558A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994655 | ||||||
chr14:64994656
|
C | T | 1 | a0001c0001t0002g0339 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.144+7559C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994656 | ||||||
chr14:64994866
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.144+7769C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994866 | ||||||
chr14:64994935
|
T | A | 2 | a0001c0001t0001g0300a0004c0002t0002g0012 | 2 | NA18956.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.144+7838T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994935 | ||||||
chr14:64994954
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+7857C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994954 | ||||||
chr14:64995277
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.144+8180A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995277 | ||||||
chr14:64995280
|
T | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.144+8183T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995280 | ||||||
chr14:64995463
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.144+8366A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995463 | ||||||
chr14:64995602
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.144+8505C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995602 | ||||||
chr14:64995727
|
A | T | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.145-8522A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995727 | ||||||
chr14:64995770
|
CGTAT | C | 3 | a0001c0001t0001g0335a0001c0001t0002g0027a0001c0001t0002g0028 | 3 | HG01243.hp1 HG02895.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.145-8458_145-8455d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64995770 | |||||
chr14:64995770
|
CGTATGTA others(1): Show |
C | 83 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.145-8462_145-8455d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64995770 | |||||
chr14:64995771
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-8478G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995771 | ||||||
chr14:64995774
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.145-8475T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995774 | ||||||
chr14:64995791
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.145-8458G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995791 | ||||||
chr14:64995903
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0002g0027a0001c0001t0002g0028others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.145-8346C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995903 | ||||||
chr14:64995906
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.145-8343G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995906 | ||||||
chr14:64995928
|
G | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0232others(3): Show | 6 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-8321G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995928 | ||||||
chr14:64995997
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-8252C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995997 | ||||||
chr14:64996037
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(9): Show | 13 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.145-8212C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996037 | ||||||
chr14:64996083
|
A | G | 1 | a0001c0001t0002g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-8166A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996083 | ||||||
chr14:64996123
|
C | CA | 20 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(17): Show | 21 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.145-8109dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996123 | |||||
chr14:64996123
|
C | CAA | 9 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0002g0027others(6): Show | 9 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.145-8110_145-8109d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996123 | |||||
chr14:64996123
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-8118_145-8109d others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996123 | |||||
chr14:64996141
|
GAAAA | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG03927.hp2 NA18955.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.145-8105_145-8102d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996141 | |||||
chr14:64996145
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.145-8104A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996145 | ||||||
chr14:64996485
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.145-7764A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996485 | ||||||
chr14:64996766
|
C | CT | 108 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0074others(105): Show | 109 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.145-7462dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | |||||
chr14:64996766
|
C | CTT | 7 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0267others(4): Show | 7 | HG00140.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.145-7463_145-7462d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | |||||
chr14:64996766
|
CT | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(14): Show | 17 | HG01515.hp1 HG01891.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.145-7462delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | |||||
chr14:64996766
|
CTT | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0020others(21): Show | 25 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.145-7463_145-7462d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | |||||
chr14:64996987
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0275 | 2 | HG01515.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.145-7262A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996987 | ||||||
chr14:64997019
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-7230T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997019 | ||||||
chr14:64997135
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.145-7114T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997135 | ||||||
chr14:64997286
|
A | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(35): Show | 40 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.145-6963A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997286 | ||||||
chr14:64997458
|
T | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 14 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-6791T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997458 | ||||||
chr14:64997584
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 113 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.145-6665T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997584 | ||||||
chr14:64997643
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.145-6606C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997643 | ||||||
chr14:64998057
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | NA18962.hp1 NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.145-6192T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998057 | ||||||
chr14:64998083
|
TA | T | 7 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0002g0035others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.145-6162delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64998083 | |||||
chr14:64998153
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0113 | 2 | NA18942.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.145-6096G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998153 | ||||||
chr14:64998219
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(31): Show | 35 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.145-6030A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998219 | ||||||
chr14:64998322
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 114 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.145-5927G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998322 | ||||||
chr14:64998341
|
A | G | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145-5908A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998341 | ||||||
chr14:64998409
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-5840A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998409 | ||||||
chr14:64998453
|
CA | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0083others(42): Show | 46 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.145-5794delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64998453 | |||||
chr14:64998504
|
G | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 14 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-5745G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998504 | ||||||
chr14:64998657
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-5592C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998657 | ||||||
chr14:64998773
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 14 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-5476A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998773 | ||||||
chr14:64998869
|
G | A | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG00408.hp2 HG00609.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-5380G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998869 | ||||||
chr14:64998975
|
T | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | NA18962.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.145-5274T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998975 | ||||||
chr14:64999007
|
A | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-5242A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999007 | ||||||
chr14:64999087
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.145-5162A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999087 | ||||||
chr14:64999162
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-5087G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999162 | ||||||
chr14:64999207
|
G | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-5042G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999207 | ||||||
chr14:64999210
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-5039T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999210 | ||||||
chr14:64999252
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-4997G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999252 | ||||||
chr14:64999446
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.145-4803A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999446 | ||||||
chr14:64999508
|
G | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.145-4741G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999508 | ||||||
chr14:64999524
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.145-4725G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999524 | ||||||
chr14:64999607
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0278 | 2 | HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.145-4642A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999607 | ||||||
chr14:64999687
|
C | A | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.145-4562C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999687 | ||||||
chr14:64999833
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.145-4416G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999833 | ||||||
chr14:64999941
|
T | G | 1 | a0001c0001t0002g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.145-4308T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999941 | ||||||
chr14:64999957
|
G | A | 7 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0002g0035others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.145-4292G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999957 | ||||||
chr14:64999994
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-4255C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999994 | ||||||
chr14:65000089
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.145-4160G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000089 | ||||||
chr14:65000229
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.145-4020C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000229 | ||||||
chr14:65000396
|
G | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 12 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-3853G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000396 | ||||||
chr14:65000572
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0193others(2): Show | 5 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-3677G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000572 | ||||||
chr14:65000596
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.145-3653A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000596 | ||||||
chr14:65000616
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.145-3633C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000616 | ||||||
chr14:65000807
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0002g0094 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.145-3442C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000807 | ||||||
chr14:65000815
|
C | CA | 21 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0127others(18): Show | 21 | HG00544.hp2 HG01081.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.145-3408dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | |||||
chr14:65000815
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-3421_145-3408d others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | |||||
chr14:65000815
|
CA | C | 94 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.145-3408delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | |||||
chr14:65000815
|
CAA | C | 13 | a0001c0001t0001g0074a0001c0001t0001g0267a0001c0001t0001g0268others(10): Show | 13 | HG00140.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.145-3409_145-3408d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | |||||
chr14:65000815
|
CAAA | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-3410_145-3408d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | |||||
chr14:65000815
|
CAAAAAAA others(2): Show |
C | 25 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(22): Show | 26 | HG00140.hp2 HG01169.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.145-3416_145-3408d others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | |||||
chr14:65000831
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.145-3418A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000831 | ||||||
chr14:65000838
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.145-3408_145-3407i others(26): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | |||||
chr14:65000838
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0266 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.145-3408_145-3407i others(25): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | |||||
chr14:65000838
|
A | AAAAAAAA others(15): Show |
4 | a0001c0001t0001g0240a0001c0001t0001g0291a0001c0001t0001g0293others(1): Show | 4 | HG02738.hp1 HG03017.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | |||||
chr14:65000838
|
A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0230a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG02698.hp1 NA18953.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(23): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | |||||
chr14:65000838
|
A | AAAAAAAA others(13): Show |
17 | a0001c0001t0001g0084a0001c0001t0001g0235a0001c0001t0001g0236others(14): Show | 17 | HG02027.hp2 HG02083.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | |||||
chr14:65000838
|
A | AAAAAAAA others(12): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0231others(9): Show | 13 | HG01099.hp2 HG01243.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | |||||
chr14:65000838
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0264 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.145-3408_145-3407i others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | |||||
chr14:65000838
|
A | AG | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0232others(2): Show | 5 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-3411_145-3410i others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000838 | ||||||
chr14:65000838
|
A | G | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | HG00140.hp1 HG01175.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-3411A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000838 | ||||||
chr14:65000863
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-3386G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000863 | ||||||
chr14:65000893
|
C | T | 1 | a0001c0005t0002g0286 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145-3356C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000893 | ||||||
chr14:65001017
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-3232T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001017 | ||||||
chr14:65001156
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-3093C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001156 | ||||||
chr14:65001226
|
A | T | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145-3023A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001226 | ||||||
chr14:65001874
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-2375C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001874 | ||||||
chr14:65002010
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.145-2239A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002010 | ||||||
chr14:65002062
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0352others(2): Show | 5 | HG02074.hp2 HG02083.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-2187G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002062 | ||||||
chr14:65002296
|
T | G | 5 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0002g0344others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-1953T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002296 | ||||||
chr14:65002312
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.145-1937A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002312 | ||||||
chr14:65002335
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 12 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-1914G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002335 | ||||||
chr14:65002344
|
C | T | 20 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(17): Show | 20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.145-1905C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002344 | ||||||
chr14:65002398
|
C | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0197 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.145-1851C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002398 | ||||||
chr14:65002414
|
G | C | 4 | a0001c0001t0001g0072a0001c0001t0002g0101a0001c0001t0002g0103others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-1835G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002414 | ||||||
chr14:65002473
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.145-1776G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002473 | ||||||
chr14:65002483
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.145-1766C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002483 | ||||||
chr14:65002561
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-1688A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002561 | ||||||
chr14:65002626
|
TA | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(34): Show | 39 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.145-1614delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65002626 | |||||
chr14:65002693
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.145-1556G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002693 | ||||||
chr14:65002721
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.145-1528G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002721 | ||||||
chr14:65002931
|
A | G | 51 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0296others(48): Show | 51 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.145-1318A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002931 | ||||||
chr14:65003212
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-1037G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003212 | ||||||
chr14:65003431
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.145-818C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003431 | ||||||
chr14:65003478
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.145-771A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003478 | ||||||
chr14:65003549
|
T | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0270others(1): Show | 4 | HG00733.hp1 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-700T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003549 | ||||||
chr14:65003731
|
A | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0019others(14): Show | 18 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.145-518A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003731 | ||||||
chr14:65003928
|
C | T | 20 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(17): Show | 20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.145-321C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003928 | ||||||
chr14:65004053
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0002g0094 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.145-196C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004053 | ||||||
chr14:65004102
|
C | G | 2 | a0001c0001t0002g0344a0001c0001t0002g0351 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.145-147C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004102 | ||||||
chr14:65004111
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.145-138C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004111 | ||||||
chr14:65004113
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 154 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.145-136A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004113 | ||||||
chr14:65004115
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.145-134C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004115 | ||||||
chr14:65004162
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.145-87T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004162 | ||||||
chr14:65004468
|
C | T | 25 | a0001c0001t0001g0030a0001c0001t0001g0080a0001c0001t0001g0092others(22): Show | 25 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.209+155C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004468 | ||||||
chr14:65004533
|
A | G | 4 | a0001c0001t0001g0349a0001c0001t0002g0209a0001c0001t0002g0210others(1): Show | 4 | HG01433.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+220A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004533 | ||||||
chr14:65004654
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209+341T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004654 | ||||||
chr14:65004693
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0057 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.209+380G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004693 | ||||||
chr14:65004745
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.209+432C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004745 | ||||||
chr14:65004772
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209+459C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004772 | ||||||
chr14:65004823
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.209+510C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004823 | ||||||
chr14:65005202
|
G | A | 24 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(21): Show | 24 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.209+889G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005202 | ||||||
chr14:65005417
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.209+1104A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005417 | ||||||
chr14:65005443
|
CCTTTCTT others(6): Show |
C | 1 | a0001c0004t0001g0105 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.209+1139_209+1151d others(15): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005443 | |||||
chr14:65005449
|
T | TTTTC | 50 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0056others(47): Show | 50 | HG00323.hp1 HG00438.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.209+1198_209+1201d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
T | TTTTCTTT others(1): Show |
12 | a0001c0001t0001g0127a0001c0001t0001g0158a0001c0001t0001g0160others(9): Show | 12 | HG00544.hp2 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.209+1194_209+1201d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
T | TTTTCTTT others(5): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0001g0306others(2): Show | 5 | HG00642.hp2 HG02698.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+1190_209+1201d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
T | TTTTCTTT others(9): Show |
1 | a0001c0001t0001g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.209+1186_209+1201d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
TTTTC | T | 45 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0057others(42): Show | 45 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.209+1198_209+1201d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
TTTTCTTT others(1): Show |
T | 33 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(30): Show | 33 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.209+1194_209+1201d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
TTTTCTTT others(5): Show |
T | 18 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 19 | HG00733.hp1 HG00735.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.209+1190_209+1201d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
TTTTCTTT others(9): Show |
T | 2 | a0001c0001t0001g0118a0001c0001t0002g0184 | 2 | HG02630.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.209+1186_209+1201d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
TTTTCTTT others(13): Show |
T | 2 | a0001c0001t0001g0211a0001c0001t0001g0341 | 2 | HG02257.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.209+1182_209+1201d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005449
|
TTTTCTTT others(21): Show |
T | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.209+1174_209+1201d others(30): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | |||||
chr14:65005453
|
C | CT | 4 | a0001c0001t0001g0289a0001c0001t0001g0301a0001c0001t0002g0089others(1): Show | 4 | HG02523.hp1 HG02615.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+1143dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005453 | |||||
chr14:65005462
|
TTTCTTTC others(4): Show |
T | 1 | a0001c0005t0002g0286 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.209+1152_209+1162d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005462 | |||||
chr14:65005482
|
TTTCTTTC others(4): Show |
T | 4 | a0001c0001t0001g0243a0001c0001t0001g0255a0001c0001t0001g0291others(1): Show | 4 | NA18939.hp2 NA18981.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+1172_209+1182d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005482 | |||||
chr14:65005491
|
TTCTTTCT others(15): Show |
T | 3 | a0001c0001t0001g0106a0001c0001t0001g0315a0001c0001t0001g0347 | 3 | HG00544.hp1 NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.209+1182_209+1203d others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005491 | |||||
chr14:65005491
|
TTCTTTCT others(17): Show |
T | 1 | a0001c0001t0002g0122 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.209+1182_209+1205d others(26): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005491 | |||||
chr14:65005495
|
TTCTTTCT others(11): Show |
T | 13 | a0001c0001t0001g0038a0001c0001t0001g0107a0001c0001t0001g0133others(10): Show | 13 | HG02074.hp2 HG02083.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.209+1186_209+1203d others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005495 | |||||
chr14:65005495
|
TTCTTTCT others(13): Show |
T | 2 | a0001c0001t0002g0097a0001c0001t0002g0123 | 2 | NA18945.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.209+1186_209+1205d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005495 | |||||
chr14:65005499
|
TTCTTTCT others(7): Show |
T | 13 | a0001c0001t0001g0037a0001c0001t0001g0194a0001c0001t0001g0196others(10): Show | 13 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.209+1190_209+1203d others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005499 | |||||
chr14:65005499
|
TTCTTTCT others(9): Show |
T | 1 | a0001c0001t0002g0096 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.209+1190_209+1205d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005499 | |||||
chr14:65005503
|
TTCTTTCT others(3): Show |
T | 23 | a0001c0001t0001g0064a0001c0001t0001g0199a0001c0001t0001g0202others(20): Show | 23 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.209+1194_209+1203d others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005503 | |||||
chr14:65005503
|
TTCTTTCT others(5): Show |
T | 1 | a0001c0001t0002g0314 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.209+1194_209+1205d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005503 | |||||
chr14:65005507
|
TTCTTTC | T | 21 | a0001c0001t0001g0068a0001c0001t0001g0204a0001c0001t0001g0205others(18): Show | 21 | HG01071.hp1 HG01081.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.209+1198_209+1203d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005507 | |||||
chr14:65005511
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0002g0079a0001c0001t0002g0200others(1): Show | 4 | HG01884.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+1198T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005511 | ||||||
chr14:65005513
|
C | CTT | 12 | a0001c0001t0001g0072a0001c0001t0001g0091a0001c0001t0001g0275others(9): Show | 12 | HG01884.hp1 HG01981.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.209+1201_209+1202i others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005513 | |||||
chr14:65005515
|
C | T | 2 | a0001c0001t0002g0103a0001c0001t0002g0197 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.209+1202C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005515 | ||||||
chr14:65005519
|
CTCTT | C | 3 | a0001c0001t0002g0035a0001c0001t0002g0132a0001c0005t0002g0286 | 3 | HG02602.hp2 HG02738.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.209+1210_209+1213d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005519 | |||||
chr14:65005521
|
CTT | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(16): Show | 20 | HG00621.hp1 HG01106.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.209+1210_209+1211d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005521 | |||||
chr14:65005523
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.209+1210T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005523 | ||||||
chr14:65005528
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209+1215T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005528 | ||||||
chr14:65005639
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.209+1326C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005639 | ||||||
chr14:65005756
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(9): Show | 12 | HG02129.hp2 HG02723.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.209+1443C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005756 | ||||||
chr14:65005785
|
A | T | 20 | a0001c0001t0002g0035a0001c0001t0002g0052a0001c0001t0002g0058others(17): Show | 20 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.209+1472A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005785 | ||||||
chr14:65005905
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0348others(2): Show | 5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1592C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005905 | ||||||
chr14:65005939
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.209+1626C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005939 | ||||||
chr14:65006156
|
C | CT | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(204): Show | 209 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.209+1860dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65006156 | |||||
chr14:65006156
|
C | CTT | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(50): Show | 53 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.209+1859_209+1860d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65006156 | |||||
chr14:65006223
|
G | A | 1 | a0003c0003t0001g0350 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.209+1910G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006223 | ||||||
chr14:65006369
|
T | C | 1 | a0001c0001t0002g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.209+2056T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006369 | ||||||
chr14:65006463
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.209+2150C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006463 | ||||||
chr14:65006478
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(238): Show | 243 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.209+2165G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006478 | ||||||
chr14:65006541
|
G | C | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.209+2228G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006541 | ||||||
chr14:65006575
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.209+2262G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006575 | ||||||
chr14:65006636
|
G | T | 1 | a0001c0001t0002g0221 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.209+2323G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006636 | ||||||
chr14:65006639
|
G | C | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.209+2326G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006639 | ||||||
chr14:65006845
|
A | T | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.209+2532A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006845 | ||||||
chr14:65006921
|
G | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0078others(1): Show | 4 | HG01884.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+2608G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006921 | ||||||
chr14:65006977
|
T | A | 1 | a0001c0001t0001g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.209+2664T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006977 | ||||||
chr14:65006978
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.209+2665T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006978 | ||||||
chr14:65007028
|
A | G | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.209+2715A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007028 | ||||||
chr14:65007157
|
G | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 242 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.209+2844G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007157 | ||||||
chr14:65007177
|
A | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.209+2864A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007177 | ||||||
chr14:65007338
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.209+3025A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007338 | ||||||
chr14:65007420
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.209+3107G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007420 | ||||||
chr14:65007456
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209+3143A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007456 | ||||||
chr14:65007653
|
G | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.209+3340G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007653 | ||||||
chr14:65007735
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.209+3422C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007735 | ||||||
chr14:65007855
|
A | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.209+3542A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007855 | ||||||
chr14:65007887
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.209+3574T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007887 | ||||||
chr14:65007905
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.209+3592T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007905 | ||||||
chr14:65008110
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209+3797C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008110 | ||||||
chr14:65008180
|
G | T | 6 | a0001c0001t0002g0061a0001c0001t0002g0066a0001c0001t0002g0067others(3): Show | 6 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+3867G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008180 | ||||||
chr14:65008292
|
G | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.209+3979G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008292 | ||||||
chr14:65008631
|
T | G | 1 | a0001c0001t0001g0354 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.210-3686T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008631 | ||||||
chr14:65008649
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-3668G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008649 | ||||||
chr14:65008670
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.210-3647A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008670 | ||||||
chr14:65008693
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.210-3624A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008693 | ||||||
chr14:65008822
|
C | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(234): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.210-3495C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008822 | ||||||
chr14:65008990
|
C | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.210-3327C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008990 | ||||||
chr14:65009353
|
C | CTGGCGCT | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-2963_210-2962i others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65009353 | |||||
chr14:65009355
|
A | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-2962A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009355 | ||||||
chr14:65009378
|
C | G | 23 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(20): Show | 23 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.210-2939C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009378 | ||||||
chr14:65009411
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.210-2906C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009411 | ||||||
chr14:65009531
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-2786C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009531 | ||||||
chr14:65009841
|
C | A | 1 | a0001c0001t0001g0311 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.210-2476C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009841 | ||||||
chr14:65009857
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0133 | 2 | NA18945.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.210-2460G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009857 | ||||||
chr14:65009893
|
G | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-2424G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009893 | ||||||
chr14:65009981
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.210-2336C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009981 | ||||||
chr14:65010160
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.210-2157C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010160 | ||||||
chr14:65010204
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.210-2113C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010204 | ||||||
chr14:65010268
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-2049G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010268 | ||||||
chr14:65010277
|
C | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-2040C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010277 | ||||||
chr14:65010636
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-1681C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010636 | ||||||
chr14:65010662
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-1655C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010662 | ||||||
chr14:65010672
|
A | G | 22 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0035others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.210-1645A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010672 | ||||||
chr14:65010681
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.210-1636A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010681 | ||||||
chr14:65010783
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.210-1534C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010783 | ||||||
chr14:65010807
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.210-1510C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010807 | ||||||
chr14:65010912
|
T | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-1405T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010912 | ||||||
chr14:65010962
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.210-1355G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010962 | ||||||
chr14:65011018
|
T | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-1299T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011018 | ||||||
chr14:65011024
|
CCCTT | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 80 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.210-1292_210-1289d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011024 | ||||||
chr14:65011193
|
C | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-1124C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011193 | ||||||
chr14:65011237
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(111): Show | 115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.210-1080G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011237 | ||||||
chr14:65011312
|
C | G | 1 | a0001c0001t0001g0323 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.210-1005C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011312 | ||||||
chr14:65011426
|
C | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-891C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011426 | ||||||
chr14:65011431
|
G | GA | 98 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0026others(95): Show | 99 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.210-865dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | |||||
chr14:65011431
|
G | GAA | 29 | a0001c0001t0001g0018a0001c0001t0001g0275a0001c0001t0001g0303others(26): Show | 29 | HG00423.hp2 HG01243.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.210-866_210-865dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | |||||
chr14:65011431
|
GA | G | 23 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0056others(20): Show | 23 | HG01099.hp1 HG01175.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.210-865delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | |||||
chr14:65011431
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0002g0191 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.210-875_210-865del others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | |||||
chr14:65011453
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.210-864G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011453 | ||||||
chr14:65011457
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-860G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011457 | ||||||
chr14:65011471
|
A | C | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-846A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011471 | ||||||
chr14:65011472
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-845C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011472 | ||||||
chr14:65011637
|
A | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0348others(2): Show | 5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-680A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011637 | ||||||
chr14:65011903
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-414C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011903 | ||||||
chr14:65012059
|
C | G | 2 | a0001c0001t0002g0142a0001c0001t0002g0187 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.210-258C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012059 | ||||||
chr14:65012065
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-252C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012065 | ||||||
chr14:65012080
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.210-237G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012080 | ||||||
chr14:65012112
|
A | T | 3 | a0001c0001t0001g0072a0001c0001t0002g0101a0001c0001t0002g0108 | 3 | HG01109.hp1 HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.210-205A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012112 | ||||||
chr14:65012205
|
A | AG | 17 | a0001c0001t0002g0052a0001c0001t0002g0058a0001c0001t0002g0059others(14): Show | 17 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.210-107dupG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65012205 | |||||
chr14:65012212
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0002g0044 | 3 | HG01175.hp2 HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.210-105C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012212 | ||||||
chr14:65012230
|
T | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.210-87T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012230 | ||||||
chr14:65012247
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210-70C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012247 | ||||||
chr14:65012248
|
G | A | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-69G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012248 | ||||||
chr14:65012253
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.210-64C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012253 | ||||||
chr14:65012253
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-64C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012253 | ||||||
chr14:65012395
|
C | T | 1 | a0001c0001t0002g0008 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.282+6C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012395 | ||||||
chr14:65012397
|
C | A | 1 | a0001c0001t0002g0120 | 1 | HG03927.hp1 | splice_region_variant&intron_variant | LOW | c.282+8C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012397 | ||||||
chr14:65012583
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.282+194C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012583 | ||||||
chr14:65012628
|
A | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+239A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012628 | ||||||
chr14:65012642
|
A | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+253A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012642 | ||||||
chr14:65012733
|
C | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0086 | 2 | HG00140.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.282+344C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012733 | ||||||
chr14:65012742
|
C | T | 2 | a0001c0001t0002g0142a0001c0001t0002g0187 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.282+353C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012742 | ||||||
chr14:65012950
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+561G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012950 | ||||||
chr14:65012953
|
T | C | 1 | a0001c0001t0002g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+564T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012953 | ||||||
chr14:65013001
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+612C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013001 | ||||||
chr14:65013248
|
T | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+859T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013248 | ||||||
chr14:65013325
|
C | CT | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 240 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.282+948dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65013325 | |||||
chr14:65013365
|
G | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | NA18970.hp2 NA18990.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+976G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013365 | ||||||
chr14:65013422
|
T | C | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1033T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013422 | ||||||
chr14:65013441
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0348others(2): Show | 5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+1052C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013441 | ||||||
chr14:65013479
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(112): Show | 116 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.282+1090C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013479 | ||||||
chr14:65013490
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 110 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.282+1101T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013490 | ||||||
chr14:65013562
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282+1173A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013562 | ||||||
chr14:65013580
|
C | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.282+1191C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013580 | ||||||
chr14:65013587
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.282+1198T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013587 | ||||||
chr14:65013737
|
A | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+1348A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013737 | ||||||
chr14:65013768
|
G | A | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.282+1379G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013768 | ||||||
chr14:65013840
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0193 | 2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.282+1451G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013840 | ||||||
chr14:65013877
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.282+1488A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013877 | ||||||
chr14:65014089
|
G | T | 1 | a0001c0001t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.283-1536G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014089 | ||||||
chr14:65014122
|
C | CT | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1502dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65014122 | |||||
chr14:65014299
|
C | A | 1 | a0001c0001t0001g0164 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.283-1326C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014299 | ||||||
chr14:65014300
|
G | A | 17 | a0001c0001t0002g0052a0001c0001t0002g0058a0001c0001t0002g0059others(14): Show | 17 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.283-1325G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014300 | ||||||
chr14:65014494
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 73 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.283-1131C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014494 | ||||||
chr14:65014675
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283-950A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014675 | ||||||
chr14:65014691
|
G | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-934G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014691 | ||||||
chr14:65014738
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0002g0125a0001c0001t0002g0177others(1): Show | 4 | NA18956.hp1 NA18990.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-887C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014738 | ||||||
chr14:65014826
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(48): Show | 51 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.283-799G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014826 | ||||||
chr14:65014933
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0272 | 3 | HG00735.hp1 HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.283-692A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014933 | ||||||
chr14:65014992
|
C | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.283-633C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014992 | ||||||
chr14:65015108
|
CT | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 110 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.283-505delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015108 | |||||
chr14:65015141
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.283-484C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015141 | ||||||
chr14:65015303
|
A | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-322A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015303 | ||||||
chr14:65015392
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-233C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015392 | ||||||
chr14:65015410
|
C | CT | 9 | a0001c0001t0001g0150a0001c0001t0001g0160a0001c0001t0001g0269others(6): Show | 9 | HG01243.hp1 HG01255.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-191dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | |||||
chr14:65015410
|
C | CTT | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.283-192_283-191dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | |||||
chr14:65015410
|
CT | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 99 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.283-191delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | |||||
chr14:65015410
|
CTT | C | 10 | a0001c0001t0001g0261a0001c0001t0001g0289a0001c0001t0002g0062others(7): Show | 10 | HG01943.hp1 HG02129.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-192_283-191del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | |||||
chr14:65015410
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-204_283-191del others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | |||||
chr14:65015417
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.283-208T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015417 | ||||||
chr14:65016006
|
C | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.374+290C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016006 | ||||||
chr14:65016018
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.374+302A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016018 | ||||||
chr14:65016155
|
C | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+439C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016155 | ||||||
chr14:65016203
|
C | G | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.374+487C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016203 | ||||||
chr14:65016461
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057 | 3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.374+745C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016461 | ||||||
chr14:65016494
|
T | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+778T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016494 | ||||||
chr14:65016570
|
C | T | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+854C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016570 | ||||||
chr14:65016577
|
GC | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+863delC | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016577 | |||||
chr14:65016712
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.374+996G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016712 | ||||||
chr14:65016724
|
A | G | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.374+1008A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016724 | ||||||
chr14:65016764
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(81): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.374+1048C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016764 | ||||||
chr14:65016837
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.374+1121C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016837 | ||||||
chr14:65016920
|
G | GT | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(187): Show | 192 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.374+1224dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | |||||
chr14:65016920
|
G | GTT | 16 | a0001c0001t0001g0072a0001c0001t0001g0091a0001c0001t0001g0222others(13): Show | 16 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.374+1223_374+1224d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | |||||
chr14:65016920
|
G | GTTTTT | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.374+1220_374+1224d others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | |||||
chr14:65016920
|
G | GTTTTTT | 6 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0047others(3): Show | 6 | HG01192.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.374+1219_374+1224d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | |||||
chr14:65016920
|
GT | G | 11 | a0001c0001t0001g0179a0001c0001t0001g0316a0001c0001t0001g0321others(8): Show | 11 | HG00621.hp1 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.374+1224delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | |||||
chr14:65017002
|
T | A | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+1286T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017002 | ||||||
chr14:65017083
|
T | C | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(350): Show | 356 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(353): Show |
intron_variant | MODIFIER | c.374+1367T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017083 | ||||||
chr14:65017084
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.374+1368G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017084 | ||||||
chr14:65017088
|
A | C | 1 | a0001c0001t0002g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.374+1372A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017088 | ||||||
chr14:65017139
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.374+1423T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017139 | ||||||
chr14:65017169
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.374+1453T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017169 | ||||||
chr14:65017286
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.374+1570C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017286 | ||||||
chr14:65017449
|
G | T | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+1733G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017449 | ||||||
chr14:65017508
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+1792T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017508 | ||||||
chr14:65017680
|
T | C | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+1964T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017680 | ||||||
chr14:65017706
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0164 | 2 | HG01257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.374+1990A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017706 | ||||||
chr14:65017736
|
A | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.374+2020A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017736 | ||||||
chr14:65017757
|
A | G | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+2041A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017757 | ||||||
chr14:65017928
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.374+2212C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017928 | ||||||
chr14:65018000
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.374+2284A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018000 | ||||||
chr14:65018084
|
G | A | 1 | a0001c0001t0002g0310 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.374+2368G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018084 | ||||||
chr14:65018107
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.374+2391C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018107 | ||||||
chr14:65018109
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0068 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.374+2393C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018109 | ||||||
chr14:65018180
|
A | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+2464A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018180 | ||||||
chr14:65018242
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.374+2526G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018242 | ||||||
chr14:65018369
|
A | G | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+2653A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018369 | ||||||
chr14:65018422
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.374+2706C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018422 | ||||||
chr14:65018718
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+3002G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018718 | ||||||
chr14:65018739
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.374+3023G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018739 | ||||||
chr14:65018809
|
T | TA | 119 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 120 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.374+3112dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | |||||
chr14:65018809
|
T | TAA | 11 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0234others(8): Show | 11 | HG01106.hp1 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.374+3111_374+3112d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | |||||
chr14:65018809
|
TAA | T | 19 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(16): Show | 19 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.374+3111_374+3112d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | |||||
chr14:65018809
|
TAAAA | T | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+3109_374+3112d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | |||||
chr14:65018829
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.374+3113G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018829 | ||||||
chr14:65018843
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.374+3127G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018843 | ||||||
chr14:65018862
|
G | C | 2 | a0001c0001t0002g0344a0001c0001t0002g0351 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.374+3146G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018862 | ||||||
chr14:65018881
|
T | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(29): Show | 32 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.374+3165T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018881 | ||||||
chr14:65018900
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.374+3184C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018900 | ||||||
chr14:65018923
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.374+3207C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018923 | ||||||
chr14:65019087
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+3371C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019087 | ||||||
chr14:65019097
|
C | T | 71 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.374+3381C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019097 | ||||||
chr14:65019129
|
C | T | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+3413C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019129 | ||||||
chr14:65019236
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+3520C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019236 | ||||||
chr14:65019262
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.374+3546G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019262 | ||||||
chr14:65019312
|
C | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 111 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.374+3596C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019312 | ||||||
chr14:65019503
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0348others(2): Show | 5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.374+3787A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019503 | ||||||
chr14:65019508
|
A | AT | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(236): Show | 241 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.374+3800dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65019508 | |||||
chr14:65019572
|
A | T | 1 | a0001c0001t0001g0340 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.374+3856A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019572 | ||||||
chr14:65019630
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+3914G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019630 | ||||||
chr14:65019737
|
A | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.374+4021A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019737 | ||||||
chr14:65019758
|
G | A | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4042G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019758 | ||||||
chr14:65019792
|
G | A | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4076G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019792 | ||||||
chr14:65019869
|
A | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4153A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019869 | ||||||
chr14:65019959
|
G | A | 1 | a0001c0004t0001g0105 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.374+4243G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019959 | ||||||
chr14:65019981
|
A | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.374+4265A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019981 | ||||||
chr14:65019989
|
T | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.374+4273T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019989 | ||||||
chr14:65020072
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.374+4356C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020072 | ||||||
chr14:65020138
|
G | A | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4422G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020138 | ||||||
chr14:65020221
|
G | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0074others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4505G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020221 | ||||||
chr14:65020330
|
C | T | 1 | a0001c0001t0002g0344 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.374+4614C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020330 | ||||||
chr14:65020434
|
CCT | C | 5 | a0001c0001t0002g0029a0001c0001t0002g0031a0001c0001t0002g0036others(2): Show | 5 | HG01074.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+4721_374+4722d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65020434 | |||||
chr14:65020456
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.374+4740C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020456 | ||||||
chr14:65020472
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+4756C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020472 | ||||||
chr14:65020654
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.374+4938G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020654 | ||||||
chr14:65020733
|
C | CT | 30 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 30 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.374+5033dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65020733 | |||||
chr14:65020733
|
C | CTT | 79 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 80 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.374+5032_374+5033d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65020733 | |||||
chr14:65020976
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.374+5260T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020976 | ||||||
chr14:65021019
|
C | T | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+5303C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021019 | ||||||
chr14:65021037
|
C | T | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+5321C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021037 | ||||||
chr14:65021078
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.374+5362T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021078 | ||||||
chr14:65021113
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+5397T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021113 | ||||||
chr14:65021479
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.374+5763A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021479 | ||||||
chr14:65021739
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.375-5714G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021739 | ||||||
chr14:65021742
|
T | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0041others(23): Show | 26 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.375-5711T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021742 | ||||||
chr14:65021749
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.375-5704G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021749 | ||||||
chr14:65021873
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0340 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.375-5580T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021873 | ||||||
chr14:65021889
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375-5564G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021889 | ||||||
chr14:65021921
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.375-5532T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021921 | ||||||
chr14:65021937
|
C | T | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.375-5516C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021937 | ||||||
chr14:65021942
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.375-5511G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021942 | ||||||
chr14:65022000
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.375-5453A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022000 | ||||||
chr14:65022055
|
A | T | 1 | a0001c0001t0002g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.375-5398A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022055 | ||||||
chr14:65022116
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.375-5337C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022116 | ||||||
chr14:65022206
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(2): Show | 5 | HG01175.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.375-5247C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022206 | ||||||
chr14:65022232
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0211 | 2 | HG00673.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.375-5221G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022232 | ||||||
chr14:65022284
|
G | GT | 101 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 102 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.375-5156dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022284 | |||||
chr14:65022284
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.375-5169G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022284 | ||||||
chr14:65022284
|
GT | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0054others(28): Show | 32 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.375-5156delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022284 | |||||
chr14:65022284
|
GTT | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-5157_375-5156d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022284 | |||||
chr14:65022349
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.375-5104G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022349 | ||||||
chr14:65022647
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375-4806A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022647 | ||||||
chr14:65022674
|
T | TA | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-4766dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022674 | |||||
chr14:65022675
|
A | T | 1 | a0001c0001t0002g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.375-4778A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022675 | ||||||
chr14:65022940
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.375-4513G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022940 | ||||||
chr14:65023001
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0233others(1): Show | 4 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.375-4452T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023001 | ||||||
chr14:65023169
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-4284C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023169 | ||||||
chr14:65023300
|
C | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.375-4153C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023300 | ||||||
chr14:65023347
|
C | T | 7 | a0001c0001t0002g0061a0001c0001t0002g0065a0001c0001t0002g0066others(4): Show | 7 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-4106C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023347 | ||||||
chr14:65023435
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.375-4018G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023435 | ||||||
chr14:65023478
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-3975A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023478 | ||||||
chr14:65023590
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0275 | 2 | HG01515.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.375-3863G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023590 | ||||||
chr14:65023860
|
G | A | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.375-3593G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023860 | ||||||
chr14:65024009
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.375-3444G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024009 | ||||||
chr14:65024103
|
T | TA | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.375-3335dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65024103 | |||||
chr14:65024162
|
G | A | 1 | a0001c0001t0001g0334 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.375-3291G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024162 | ||||||
chr14:65024230
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.375-3223T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024230 | ||||||
chr14:65024240
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.375-3213G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024240 | ||||||
chr14:65024328
|
A | AT | 76 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 77 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.375-3118dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65024328 | |||||
chr14:65024328
|
AT | A | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-3118delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65024328 | |||||
chr14:65024537
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 250 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.375-2916A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024537 | ||||||
chr14:65024565
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(81): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.375-2888A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024565 | ||||||
chr14:65024574
|
G | A | 20 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.375-2879G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024574 | ||||||
chr14:65024594
|
T | G | 74 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.375-2859T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024594 | ||||||
chr14:65024768
|
C | G | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.375-2685C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024768 | ||||||
chr14:65024791
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-2662T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024791 | ||||||
chr14:65024908
|
T | C | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.375-2545T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024908 | ||||||
chr14:65024929
|
G | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0149 | 2 | HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.375-2524G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024929 | ||||||
chr14:65025022
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.375-2431A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025022 | ||||||
chr14:65025035
|
A | G | 3 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0237 | 3 | HG02615.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.375-2418A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025035 | ||||||
chr14:65025086
|
C | T | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.375-2367C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025086 | ||||||
chr14:65025197
|
G | C | 6 | a0001c0001t0002g0168a0001c0001t0002g0183a0001c0001t0002g0191others(3): Show | 6 | HG02165.hp2 NA18950.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.375-2256G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025197 | ||||||
chr14:65025226
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.375-2227A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025226 | ||||||
chr14:65025484
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.375-1969C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025484 | ||||||
chr14:65025636
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.375-1817G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025636 | ||||||
chr14:65025982
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(30): Show | 33 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.375-1471T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025982 | ||||||
chr14:65026238
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.375-1215A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026238 | ||||||
chr14:65026273
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-1180G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026273 | ||||||
chr14:65026408
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375-1045T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026408 | ||||||
chr14:65026420
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.375-1033G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026420 | ||||||
chr14:65026429
|
T | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0180 | 2 | NA18984.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.375-1024T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026429 | ||||||
chr14:65026462
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375-991G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026462 | ||||||
chr14:65026522
|
G | A | 1 | a0001c0001t0002g0339 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.375-931G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026522 | ||||||
chr14:65026568
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.375-885T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026568 | ||||||
chr14:65026608
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.375-845C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026608 | ||||||
chr14:65026617
|
G | T | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.375-836G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026617 | ||||||
chr14:65026618
|
C | G | 1 | a0001c0001t0001g0349 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.375-835C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026618 | ||||||
chr14:65026646
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.375-807G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026646 | ||||||
chr14:65026696
|
A | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-757A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026696 | ||||||
chr14:65026726
|
A | G | 3 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0237 | 3 | HG02615.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.375-727A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026726 | ||||||
chr14:65026735
|
G | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-718G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026735 | ||||||
chr14:65026873
|
C | A | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.375-580C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026873 | ||||||
chr14:65026881
|
C | A | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.375-572C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026881 | ||||||
chr14:65027205
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.375-248T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65027205 | ||||||
chr14:65027231
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.375-222G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65027231 | ||||||
chr14:65027416
|
C | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0164 | 2 | HG01257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.375-37C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65027416 | ||||||
chr14:65027856
|
AGGAACAT others(4): Show |
A | 1 | a0001c0001t0002g0168 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.605+78_605+88delAA others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65027856 | |||||
chr14:65028059
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.605+278A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028059 | ||||||
chr14:65028060
|
T | A | 1 | a0001c0001t0001g0272 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.605+279T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028060 | ||||||
chr14:65028179
|
T | C | 1 | a0001c0001t0001g0323 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.605+398T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028179 | ||||||
chr14:65028236
|
G | A | 1 | a0001c0001t0005g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.605+455G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028236 | ||||||
chr14:65028278
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.605+497C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028278 | ||||||
chr14:65028611
|
C | T | 2 | a0001c0001t0003g0039a0001c0001t0003g0040 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.605+830C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028611 | ||||||
chr14:65028907
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.605+1126A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028907 | ||||||
chr14:65028908
|
CTAAGAT | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.605+1130_605+1135d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65028908 | |||||
chr14:65029092
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.605+1311C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029092 | ||||||
chr14:65029098
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(260): Show | 266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.605+1317A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029098 | ||||||
chr14:65029255
|
A | AC | 4 | a0001c0001t0001g0263a0001c0001t0001g0309a0001c0001t0001g0354others(1): Show | 4 | HG01891.hp1 HG01934.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+1478dupC | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65029255 | |||||
chr14:65029266
|
A | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+1485A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029266 | ||||||
chr14:65029523
|
A | G | 1 | a0001c0001t0002g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.605+1742A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029523 | ||||||
chr14:65029570
|
A | G | 1 | a0001c0001t0001g0334 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.605+1789A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029570 | ||||||
chr14:65029648
|
G | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.605+1867G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029648 | ||||||
chr14:65029730
|
A | C | 4 | a0001c0001t0001g0283a0001c0001t0002g0034a0001c0001t0002g0113others(1): Show | 4 | NA18942.hp2 NA18955.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+1949A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029730 | ||||||
chr14:65030084
|
C | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+2303C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030084 | ||||||
chr14:65030091
|
C | G | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.605+2310C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030091 | ||||||
chr14:65030145
|
G | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.605+2364G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030145 | ||||||
chr14:65030207
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.606-2403G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030207 | ||||||
chr14:65030279
|
A | C | 1 | a0001c0001t0002g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.606-2331A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030279 | ||||||
chr14:65030492
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.606-2118A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030492 | ||||||
chr14:65030598
|
C | T | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.606-2012C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030598 | ||||||
chr14:65030722
|
A | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.606-1888A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030722 | ||||||
chr14:65030747
|
A | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.606-1863A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030747 | ||||||
chr14:65030793
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.606-1817C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030793 | ||||||
chr14:65030806
|
C | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 169 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.606-1804C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030806 | ||||||
chr14:65030829
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.606-1781A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030829 | ||||||
chr14:65030955
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.606-1655G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030955 | ||||||
chr14:65031004
|
C | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.606-1606C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031004 | ||||||
chr14:65031467
|
G | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0233others(3): Show | 6 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-1143G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031467 | ||||||
chr14:65031638
|
A | T | 1 | a0001c0001t0002g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.606-972A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031638 | ||||||
chr14:65031695
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.606-915T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031695 | ||||||
chr14:65031696
|
G | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.606-914G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031696 | ||||||
chr14:65031775
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.606-835G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031775 | ||||||
chr14:65031778
|
A | G | 21 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.606-832A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031778 | ||||||
chr14:65031794
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.606-816G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031794 | ||||||
chr14:65031900
|
G | A | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.606-710G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031900 | ||||||
chr14:65031979
|
C | CGT | 74 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 76 | HG00140.hp1 HG00597.hp1 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.606-592_606-591dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGT | 16 | a0001c0001t0001g0083a0001c0001t0001g0115a0001c0001t0001g0117others(13): Show | 16 | HG00609.hp1 HG00642.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.606-594_606-591dup others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGT | 8 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0074others(5): Show | 8 | HG00408.hp2 HG00642.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-596_606-591dup others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0181 | 3 | HG02056.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.606-598_606-591dup others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0284 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.606-600_606-591dup others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.606-602_606-591dup others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGTG others(13): Show |
1 | a0001c0001t0002g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.606-610_606-591dup others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGTG others(15): Show |
1 | a0001c0001t0002g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.606-612_606-591dup others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGTG others(17): Show |
1 | a0001c0001t0002g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.606-614_606-591dup others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
C | CGTGTGTG others(29): Show |
1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.606-626_606-591dup others(36): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
CGT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0030others(49): Show | 53 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.606-592_606-591del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
CGTGTGT | C | 27 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(24): Show | 27 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.606-596_606-591del others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65031979
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0111 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.606-604_606-591del others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | |||||
chr14:65032307
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.606-303C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65032307 | ||||||
chr14:65032499
|
A | G | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0065others(5): Show | 8 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-111A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65032499 | ||||||
chr14:65032573
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.606-37G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65032573 | ||||||
chr14:65032730
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.692+34G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032730 | ||||||
chr14:65032732
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 122 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.692+36G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032732 | ||||||
chr14:65032736
|
A | G | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.692+40A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032736 | ||||||
chr14:65032745
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 122 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.692+49C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032745 | ||||||
chr14:65032859
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.692+163C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032859 | ||||||
chr14:65032910
|
T | TA | 76 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 77 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.692+220dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65032910 | |||||
chr14:65033000
|
C | T | 5 | a0001c0001t0002g0110a0001c0001t0002g0131a0001c0001t0002g0135others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.692+304C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033000 | ||||||
chr14:65033038
|
C | T | 10 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0239others(7): Show | 10 | HG00140.hp1 HG01123.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.692+342C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033038 | ||||||
chr14:65033191
|
T | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(245): Show | 250 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.692+495T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033191 | ||||||
chr14:65033358
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0002g0238 | 3 | HG02145.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.692+662G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033358 | ||||||
chr14:65033431
|
G | A | 70 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(67): Show | 70 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.692+735G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033431 | ||||||
chr14:65033454
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.692+758A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033454 | ||||||
chr14:65033679
|
C | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(245): Show | 250 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.692+983C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033679 | ||||||
chr14:65033745
|
T | A | 22 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(19): Show | 22 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.692+1049T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033745 | ||||||
chr14:65033750
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.692+1054G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033750 | ||||||
chr14:65033754
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.692+1058A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033754 | ||||||
chr14:65033788
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0151 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.692+1092C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033788 | ||||||
chr14:65033887
|
A | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.692+1191A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033887 | ||||||
chr14:65034017
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(262): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.692+1321A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034017 | ||||||
chr14:65034311
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(2): Show | 5 | HG01175.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.692+1615C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034311 | ||||||
chr14:65034353
|
T | G | 1 | a0001c0001t0001g0322 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.692+1657T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034353 | ||||||
chr14:65034462
|
TTGGCAA | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.692+1770_692+1775d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65034462 | |||||
chr14:65034811
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.692+2115C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034811 | ||||||
chr14:65035222
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.692+2526G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035222 | ||||||
chr14:65035283
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.692+2587A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035283 | ||||||
chr14:65035284
|
G | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 110 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.692+2588G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035284 | ||||||
chr14:65035294
|
G | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.692+2598G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035294 | ||||||
chr14:65035363
|
C | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0348others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.692+2667C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035363 | ||||||
chr14:65035375
|
G | A | 22 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(19): Show | 22 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.692+2679G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035375 | ||||||
chr14:65035402
|
G | C | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.692+2706G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035402 | ||||||
chr14:65035521
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(261): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.692+2825G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035521 | ||||||
chr14:65035530
|
TTCTC | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.692+2838_692+2841d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65035530 | |||||
chr14:65035553
|
C | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.692+2857C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035553 | ||||||
chr14:65035634
|
A | G | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.692+2938A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035634 | ||||||
chr14:65035667
|
C | G | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.692+2971C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035667 | ||||||
chr14:65035713
|
T | A | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.692+3017T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035713 | ||||||
chr14:65035856
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.692+3160A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035856 | ||||||
chr14:65036196
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0001g0345 | 2 | HG00423.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.692+3500T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036196 | ||||||
chr14:65036211
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.692+3515G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036211 | ||||||
chr14:65036243
|
T | A | 11 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(8): Show | 11 | HG01981.hp2 HG02129.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.692+3547T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036243 | ||||||
chr14:65036429
|
G | T | 43 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(40): Show | 43 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.692+3733G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036429 | ||||||
chr14:65036590
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0291 | 2 | NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.692+3894C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036590 | ||||||
chr14:65036607
|
G | A | 8 | a0001c0001t0001g0163a0001c0001t0002g0124a0001c0001t0002g0125others(5): Show | 8 | HG01981.hp2 NA18956.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.692+3911G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036607 | ||||||
chr14:65036687
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0064a0001c0001t0001g0068others(2): Show | 5 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.692+3991C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036687 | ||||||
chr14:65036699
|
ATTC | A | 10 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0239others(7): Show | 10 | HG00140.hp1 HG01123.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.692+4006_692+4008d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65036699 | |||||
chr14:65036754
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0167 | 2 | NA18954.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.693-4036C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036754 | ||||||
chr14:65036755
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 77 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.693-4035G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036755 | ||||||
chr14:65037077
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091others(1): Show | 5 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.693-3713C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037077 | ||||||
chr14:65037261
|
G | A | 26 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0035others(23): Show | 26 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-3529G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037261 | ||||||
chr14:65037287
|
AG | A | 3 | a0001c0001t0001g0072a0001c0001t0002g0101a0001c0001t0002g0108 | 3 | HG01109.hp1 HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.693-3502delG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037287 | ||||||
chr14:65037346
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0002g0200 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-3444G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037346 | ||||||
chr14:65037395
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.693-3395G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037395 | ||||||
chr14:65037402
|
C | CT | 11 | a0001c0001t0001g0043a0001c0001t0001g0156a0001c0001t0001g0196others(8): Show | 11 | HG01515.hp2 HG02280.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.693-3388_693-3387i others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTT | 9 | a0001c0001t0001g0019a0001c0001t0001g0275a0001c0001t0002g0052others(6): Show | 9 | HG01106.hp2 HG01109.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.693-3388_693-3387i others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTCTTTT others(1): Show |
5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(2): Show | 5 | HG00735.hp2 HG01169.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.693-3388_693-3387i others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTCTTTT others(3): Show |
2 | a0001c0001t0001g0022a0001c0001t0002g0011 | 2 | HG02148.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTCTTTT others(4): Show |
1 | a0001c0001t0001g0086 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.693-3388_693-3387i others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTCTTTT others(5): Show |
1 | a0001c0001t0001g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTCTTTT others(9): Show |
1 | a0001c0001t0002g0032 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.693-3388_693-3387i others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTCTTTT others(20): Show |
1 | a0001c0001t0001g0046 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(29): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTCTTTT others(26): Show |
1 | a0001c0001t0001g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(35): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTT | 3 | a0001c0001t0001g0037a0001c0001t0001g0296a0001c0001t0002g0134 | 3 | HG02630.hp2 HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTTTT | 3 | a0001c0001t0001g0303a0001c0001t0002g0059a0001c0001t0002g0104 | 3 | HG03098.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0062a0001c0001t0002g0065a0001c0001t0002g0109 | 3 | HG03195.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(19): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCT | C | 5 | a0001c0001t0001g0144a0001c0001t0001g0189a0001c0001t0002g0125others(2): Show | 5 | HG00438.hp1 HG01361.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.693-3387_693-3386d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTT | C | 22 | a0001c0001t0001g0075a0001c0001t0001g0143a0001c0001t0001g0157others(19): Show | 22 | HG00735.hp1 HG01123.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.693-3387_693-3385d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTT | C | 50 | a0001c0001t0001g0017a0001c0001t0001g0076a0001c0001t0001g0098others(47): Show | 50 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.693-3387_693-3384d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTT | C | 43 | a0001c0001t0001g0033a0001c0001t0001g0111a0001c0001t0001g0112others(40): Show | 43 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.693-3387_693-3383d others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTT | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 37 | HG00609.hp1 HG01081.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.693-3387_693-3382d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT | C | 17 | a0001c0001t0001g0057a0001c0001t0001g0083a0001c0001t0001g0128others(14): Show | 17 | HG00140.hp1 HG00642.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.693-3387_693-3381d others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0063others(7): Show | 10 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.693-3387_693-3380d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.693-3387_693-3378d others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(4): Show |
C | 4 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0027others(1): Show | 4 | HG01081.hp2 HG01175.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-3387_693-3377d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0005a0001c0001t0002g0028a0001c0001t0002g0195 | 3 | HG01243.hp1 HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3376d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.693-3387_693-3375d others(15): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0090a0001c0001t0002g0237a0004c0002t0002g0012 | 3 | HG02615.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3374d others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(8): Show |
C | 28 | a0001c0001t0001g0001a0001c0001t0001g0091a0001c0001t0001g0199others(25): Show | 29 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.693-3387_693-3373d others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(9): Show |
C | 36 | a0001c0001t0001g0018a0001c0001t0001g0077a0001c0001t0001g0106others(33): Show | 36 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.693-3387_693-3372d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0054a0001c0001t0002g0036a0001c0001t0002g0344 | 3 | HG03453.hp1 HG03927.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3371d others(19): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.693-3387_693-3370d others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0330a0001c0001t0002g0003 | 3 | HG02015.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.693-3387_693-3369d others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(13): Show |
C | 3 | a0001c0001t0001g0041a0001c0001t0001g0133a0001c0001t0002g0081 | 3 | HG02970.hp1 HG04204.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3368d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(14): Show |
C | 7 | a0001c0001t0001g0030a0001c0001t0001g0064a0001c0001t0001g0068others(4): Show | 7 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.693-3387_693-3367d others(23): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(15): Show |
C | 23 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(20): Show | 23 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.693-3387_693-3366d others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(16): Show |
C | 2 | a0001c0001t0001g0145a0001c0001t0002g0338 | 2 | HG06807.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.693-3387_693-3365d others(25): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037402
|
CCTTTTTT others(18): Show |
C | 1 | a0001c0001t0005g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.693-3387_693-3363d others(27): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | ||||||
chr14:65037403
|
C | T | 52 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 52 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.693-3387C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037403 | ||||||
chr14:65037410
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.693-3380T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037410 | ||||||
chr14:65037413
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0047 | 2 | HG00140.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.693-3377T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037413 | ||||||
chr14:65037417
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.693-3373T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037417 | ||||||
chr14:65037606
|
G | A | 6 | a0001c0001t0002g0168a0001c0001t0002g0183a0001c0001t0002g0191others(3): Show | 6 | HG02165.hp2 NA18950.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-3184G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037606 | ||||||
chr14:65037676
|
C | T | 26 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-3114C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037676 | ||||||
chr14:65037677
|
G | A | 7 | a0001c0001t0001g0204a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG01943.hp2 HG02129.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-3113G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037677 | ||||||
chr14:65037704
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0068 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.693-3086T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037704 | ||||||
chr14:65037726
|
C | CTTAT | 10 | a0001c0001t0001g0167a0001c0001t0001g0236a0001c0001t0001g0243others(7): Show | 10 | HG01891.hp2 HG02622.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.693-3050_693-3047d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037726 | |||||
chr14:65037726
|
CTTATTTA others(8): Show |
C | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.693-3046_693-3032d others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037726 | |||||
chr14:65037726
|
CTTATTTA others(12): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.693-3046_693-3028d others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037726 | |||||
chr14:65037730
|
TTTATTTA others(4): Show |
T | 29 | a0001c0001t0001g0025a0001c0001t0001g0054a0001c0001t0001g0056others(26): Show | 29 | HG00323.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.693-3046_693-3036d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037730 | |||||
chr14:65037734
|
TTTATTTA | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(43): Show | 46 | HG00423.hp1 HG00673.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.693-3046_693-3040d others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037734 | |||||
chr14:65037737
|
ATTTATTA others(5): Show |
A | 1 | a0001c0001t0001g0334 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.693-3050_693-3039d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037737 | |||||
chr14:65037738
|
TTTA | T | 48 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0001t0001g0074others(45): Show | 49 | HG00323.hp1 HG00597.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.693-3046_693-3044d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037738 | |||||
chr14:65037741
|
A | AT | 10 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0046others(7): Show | 10 | HG00140.hp2 HG00733.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.693-3047dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | |||||
chr14:65037741
|
ATTAT | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 22 | HG00642.hp2 HG01255.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.693-2995_693-2992d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | |||||
chr14:65037741
|
ATTATTTA others(1): Show |
A | 19 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0297others(16): Show | 19 | HG00597.hp2 HG01433.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.693-2999_693-2992d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | |||||
chr14:65037741
|
ATTATTTA others(5): Show |
A | 54 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.693-3003_693-2992d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | |||||
chr14:65037741
|
ATTATTTA others(9): Show |
A | 3 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0002g0109 | 3 | HG02293.hp1 NA18522.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.693-3007_693-2992d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | |||||
chr14:65037741
|
ATTATTTA others(13): Show |
A | 8 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0001g0303others(5): Show | 8 | HG01891.hp1 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.693-3011_693-2992d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | |||||
chr14:65037744
|
A | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(107): Show | 111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.693-3046A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037744 | ||||||
chr14:65037745
|
T | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 104 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.693-3045T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037745 | ||||||
chr14:65037745
|
T | TTTA | 3 | a0001c0001t0001g0045a0001c0001t0001g0270a0001c0001t0001g0349 | 3 | HG00733.hp1 HG02300.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.693-3042_693-3040d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037745 | |||||
chr14:65037748
|
A | T | 58 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(55): Show | 59 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.693-3042A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037748 | ||||||
chr14:65037748
|
AT | A | 46 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0047others(43): Show | 47 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.693-3039delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037748 | |||||
chr14:65037751
|
TA | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0235a0001c0001t0001g0253others(3): Show | 6 | HG02055.hp2 HG02083.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-3038delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037751 | ||||||
chr14:65037752
|
A | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.693-3038A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037752 | ||||||
chr14:65037752
|
AT | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0026others(18): Show | 21 | HG00733.hp2 HG01071.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.693-3035delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037752 | |||||
chr14:65037756
|
AT | A | 52 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.693-3031delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037756 | |||||
chr14:65037760
|
AT | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0185a0001c0001t0002g0120 | 3 | HG01169.hp1 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.693-3027delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037760 | |||||
chr14:65037863
|
T | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.693-2927T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037863 | ||||||
chr14:65037875
|
G | C | 1 | a0001c0001t0002g0344 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-2915G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037875 | ||||||
chr14:65037882
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.693-2908C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037882 | ||||||
chr14:65037883
|
G | A | 15 | a0001c0001t0001g0077a0001c0001t0001g0174a0001c0001t0001g0304others(12): Show | 15 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.693-2907G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037883 | ||||||
chr14:65038055
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.693-2735G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038055 | ||||||
chr14:65038186
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0064others(3): Show | 6 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.693-2604G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038186 | ||||||
chr14:65038192
|
C | T | 1 | a0001c0001t0001g0353 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.693-2598C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038192 | ||||||
chr14:65038343
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.693-2447G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038343 | ||||||
chr14:65038359
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0053others(1): Show | 4 | NA18964.hp1 NA18978.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-2431G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038359 | ||||||
chr14:65038501
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.693-2289C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038501 | ||||||
chr14:65038605
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.693-2185G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038605 | ||||||
chr14:65038761
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.693-2029G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038761 | ||||||
chr14:65038809
|
T | C | 24 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(21): Show | 24 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.693-1981T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038809 | ||||||
chr14:65038927
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-1863T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038927 | ||||||
chr14:65038979
|
C | G | 26 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-1811C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038979 | ||||||
chr14:65039115
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.693-1675G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039115 | ||||||
chr14:65039143
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0264 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.693-1647G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039143 | ||||||
chr14:65039211
|
G | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | NA18970.hp2 NA18990.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-1579G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039211 | ||||||
chr14:65039310
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0002g0088 | 2 | HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.693-1480A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039310 | ||||||
chr14:65039336
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(82): Show | 86 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.693-1454G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039336 | ||||||
chr14:65039346
|
T | A | 26 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-1444T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039346 | ||||||
chr14:65039352
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-1438C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039352 | ||||||
chr14:65039460
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.693-1330G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039460 | ||||||
chr14:65039603
|
C | A | 1 | a0001c0001t0002g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.693-1187C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039603 | ||||||
chr14:65039791
|
T | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(5): Show | 8 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.693-999T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039791 | ||||||
chr14:65039931
|
G | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.693-859G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039931 | ||||||
chr14:65039999
|
G | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.693-791G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039999 | ||||||
chr14:65040011
|
A | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-779A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040011 | ||||||
chr14:65040016
|
C | G | 1 | a0001c0001t0002g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.693-774C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040016 | ||||||
chr14:65040043
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-747G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040043 | ||||||
chr14:65040155
|
C | T | 1 | a0001c0001t0004g0325 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.693-635C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040155 | ||||||
chr14:65040208
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-582C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040208 | ||||||
chr14:65040210
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 122 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.693-580A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040210 | ||||||
chr14:65040224
|
T | G | 26 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-566T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040224 | ||||||
chr14:65040247
|
C | A | 26 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-543C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040247 | ||||||
chr14:65040257
|
A | ATGTATAT others(17): Show |
1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.693-521_693-498dup others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040257 | |||||
chr14:65040257
|
A | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(53): Show | 56 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.693-533A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040257 | ||||||
chr14:65040271
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.693-511_693-500del others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040271 | |||||
chr14:65040283
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0004t0001g0105 | 3 | NA18979.hp2 NA18981.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.693-507G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040283 | ||||||
chr14:65040283
|
GTA | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.693-495_693-494del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040283 | |||||
chr14:65040285
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0092 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.693-494_693-493ins others(30): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040285 | |||||
chr14:65040285
|
A | ATATATAT others(21): Show |
25 | a0001c0001t0001g0080a0001c0001t0001g0118a0001c0001t0001g0127others(22): Show | 25 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.693-480_693-479ins others(28): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040285 | |||||
chr14:65040285
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.693-505A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040285 | ||||||
chr14:65040329
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0335a0001c0001t0001g0356 | 3 | HG00597.hp2 NA19001.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.693-461A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040329 | ||||||
chr14:65040400
|
T | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0296 | 3 | HG02683.hp1 HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.693-390T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040400 | ||||||
chr14:65040416
|
G | A | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-374G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040416 | ||||||
chr14:65040483
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0115others(18): Show | 22 | HG00408.hp2 HG00609.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.693-307C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040483 | ||||||
chr14:65040525
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.693-265C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040525 | ||||||
chr14:65040561
|
C | T | 1 | a0001c0001t0002g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.693-229C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040561 | ||||||
chr14:65040604
|
C | CT | 134 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(131): Show | 134 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.693-166dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040604 | |||||
chr14:65040604
|
C | CTT | 12 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0030others(9): Show | 13 | HG01496.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-167_693-166dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040604 | |||||
chr14:65040604
|
CT | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(20): Show | 23 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.693-166delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040604 | |||||
chr14:65040662
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.693-128T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040662 | ||||||
chr14:65040936
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.822+17C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65040936 | ||||||
chr14:65040958
|
G | C | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.822+39G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65040958 | ||||||
chr14:65040991
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.822+72G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65040991 | ||||||
chr14:65041137
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.822+218C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041137 | ||||||
chr14:65041173
|
A | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+254A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041173 | ||||||
chr14:65041202
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.822+283A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041202 | ||||||
chr14:65041414
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.822+495A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041414 | ||||||
chr14:65041489
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.822+570A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041489 | ||||||
chr14:65041640
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.822+721G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041640 | ||||||
chr14:65041871
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+952A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041871 | ||||||
chr14:65042268
|
C | T | 355 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(352): Show | 358 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(355): Show |
intron_variant | MODIFIER | c.822+1349C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042268 | ||||||
chr14:65042351
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.822+1432C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042351 | ||||||
chr14:65042426
|
G | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.822+1507G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042426 | ||||||
chr14:65042621
|
C | A | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.823-1690C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042621 | ||||||
chr14:65042658
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.823-1653T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042658 | ||||||
chr14:65042828
|
T | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0064a0001c0001t0001g0068others(2): Show | 5 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-1483T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042828 | ||||||
chr14:65042901
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.823-1410A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042901 | ||||||
chr14:65043002
|
T | C | 1 | a0001c0001t0001g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823-1309T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043002 | ||||||
chr14:65043160
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(247): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.823-1151C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043160 | ||||||
chr14:65043161
|
G | A | 8 | a0001c0001t0001g0075a0001c0001t0001g0165a0001c0001t0001g0167others(5): Show | 8 | HG03239.hp2 HG03831.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-1150G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043161 | ||||||
chr14:65043307
|
G | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-1004G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043307 | ||||||
chr14:65043354
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.823-957C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043354 | ||||||
chr14:65043459
|
C | G | 1 | a0001c0001t0002g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-852C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043459 | ||||||
chr14:65043618
|
C | T | 25 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0127others(22): Show | 25 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.823-693C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043618 | ||||||
chr14:65043641
|
T | C | 20 | a0001c0001t0002g0052a0001c0001t0002g0058a0001c0001t0002g0059others(17): Show | 20 | HG02280.hp2 HG02572.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.823-670T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043641 | ||||||
chr14:65043668
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(248): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.823-643A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043668 | ||||||
chr14:65043691
|
G | A | 1 | a0004c0002t0002g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.823-620G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043691 | ||||||
chr14:65043715
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.823-596G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043715 | ||||||
chr14:65043779
|
G | A | 1 | a0001c0001t0001g0326 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.823-532G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043779 | ||||||
chr14:65043802
|
C | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-509C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043802 | ||||||
chr14:65043808
|
G | A | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.823-503G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043808 | ||||||
chr14:65043815
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0185 | 2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.823-496C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043815 | ||||||
chr14:65043823
|
C | T | 1 | a0003c0003t0001g0350 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.823-488C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043823 | ||||||
chr14:65043828
|
C | CA | 43 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0111others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.823-451dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
C | CAA | 11 | a0001c0001t0001g0143a0001c0001t0001g0179a0001c0001t0001g0349others(8): Show | 11 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-452_823-451dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
C | CAAA | 7 | a0001c0001t0001g0150a0001c0001t0001g0281a0001c0001t0002g0010others(4): Show | 7 | HG01074.hp2 HG01192.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-453_823-451dup others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.823-469_823-451dup others(19): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CA | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0054a0001c0001t0001g0056others(7): Show | 10 | HG00323.hp1 HG01123.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-451delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAA | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0041others(16): Show | 19 | HG01099.hp2 HG01243.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-452_823-451del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAAA | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(51): Show | 55 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.823-453_823-451del others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAAAAAAA | C | 7 | a0001c0001t0001g0080a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG00621.hp2 HG02129.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-457_823-451del others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAAAAAAA others(1): Show |
C | 24 | a0001c0001t0001g0092a0001c0001t0001g0118a0001c0001t0001g0127others(21): Show | 24 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.823-458_823-451del others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAAAAAAA others(4): Show |
C | 11 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0072others(8): Show | 11 | HG01123.hp1 HG01884.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-461_823-451del others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAAAAAAA others(5): Show |
C | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 100 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.823-462_823-451del others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0203a0001c0001t0002g0035a0001c0001t0002g0103 | 3 | HG01169.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.823-463_823-451del others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043828
|
CAAAAAAA others(7): Show |
C | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-464_823-451del others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | |||||
chr14:65043854
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.823-457A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043854 | ||||||
chr14:65043860
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823-451A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043860 | ||||||
chr14:65043964
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.823-347T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043964 | ||||||
chr14:65044115
|
T | C | 3 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0237 | 3 | HG02615.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.823-196T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65044115 | ||||||
chr14:65044248
|
T | C | 26 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.823-63T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65044248 | ||||||
chr14:65044253
|
C | T | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-58C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65044253 | ||||||
chr14:65044457
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+14G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044457 | ||||||
chr14:65044525
|
T | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0272 | 3 | HG00735.hp1 HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.955+82T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044525 | ||||||
chr14:65044700
|
G | A | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+257G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044700 | ||||||
chr14:65044703
|
G | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0240a0001c0001t0001g0250 | 3 | HG01261.hp1 HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.955+260G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044703 | ||||||
chr14:65044711
|
G | A | 26 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.955+268G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044711 | ||||||
chr14:65044726
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.955+283G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044726 | ||||||
chr14:65045126
|
TTCTC | T | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+689_955+692del others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65045126 | |||||
chr14:65045180
|
T | C | 1 | a0001c0001t0002g0351 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.955+737T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045180 | ||||||
chr14:65045329
|
A | G | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+886A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045329 | ||||||
chr14:65045409
|
G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0020others(16): Show | 20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.955+966G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045409 | ||||||
chr14:65045424
|
C | T | 1 | a0001c0001t0001g0354 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.955+981C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045424 | ||||||
chr14:65045434
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.955+991G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045434 | ||||||
chr14:65045659
|
G | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.955+1216G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045659 | ||||||
chr14:65045711
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0132 | 3 | HG02723.hp1 HG02738.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.955+1268C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045711 | ||||||
chr14:65045777
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.955+1334C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045777 | ||||||
chr14:65045840
|
G | A | 1 | a0001c0001t0002g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.955+1397G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045840 | ||||||
chr14:65046031
|
A | C | 1 | a0001c0001t0001g0290 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.955+1588A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046031 | ||||||
chr14:65046134
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0002g0044 | 3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.955+1691G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046134 | ||||||
chr14:65046196
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.955+1753G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046196 | ||||||
chr14:65046217
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.955+1774C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046217 | ||||||
chr14:65046219
|
G | C | 1 | a0001c0001t0002g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.955+1776G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046219 | ||||||
chr14:65046470
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.955+2027G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046470 | ||||||
chr14:65046548
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.955+2105G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046548 | ||||||
chr14:65046748
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.955+2305G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046748 | ||||||
chr14:65046795
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.955+2352G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046795 | ||||||
chr14:65046852
|
G | GCTT | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(250): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.955+2412_955+2414d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65046852 | |||||
chr14:65047117
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.955+2674T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047117 | ||||||
chr14:65047378
|
C | G | 1 | a0001c0001t0001g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.955+2935C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047378 | ||||||
chr14:65047450
|
A | C | 27 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0150others(24): Show | 27 | HG00438.hp1 HG01981.hp2 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.955+3007A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047450 | ||||||
chr14:65047872
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.955+3429G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047872 | ||||||
chr14:65047978
|
A | AT | 28 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0084others(25): Show | 28 | HG00673.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.955+3562dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | |||||
chr14:65047978
|
AT | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(201): Show | 206 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.955+3562delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | |||||
chr14:65047978
|
ATT | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0056a0001c0001t0001g0064others(11): Show | 14 | HG00323.hp1 HG00408.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.955+3561_955+3562d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | |||||
chr14:65047978
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0334 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.955+3552_955+3562d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | |||||
chr14:65048082
|
A | G | 1 | a0001c0001t0001g0305 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.955+3639A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048082 | ||||||
chr14:65048127
|
G | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0053others(1): Show | 4 | NA18964.hp1 NA18978.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+3684G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048127 | ||||||
chr14:65048197
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.955+3754G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048197 | ||||||
chr14:65048325
|
T | TA | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(104): Show | 107 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.955+3895dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65048325 | |||||
chr14:65048560
|
G | A | 1 | a0001c0001t0002g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+4117G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048560 | ||||||
chr14:65048663
|
G | A | 25 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0127others(22): Show | 25 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.955+4220G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048663 | ||||||
chr14:65048678
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.955+4235G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048678 | ||||||
chr14:65048710
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.955+4267C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048710 | ||||||
chr14:65048865
|
G | T | 1 | a0001c0001t0002g0010 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.956-4373G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048865 | ||||||
chr14:65048866
|
C | G | 1 | a0001c0001t0002g0010 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.956-4372C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048866 | ||||||
chr14:65049040
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.956-4198T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049040 | ||||||
chr14:65049059
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.956-4179G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049059 | ||||||
chr14:65049084
|
G | A | 6 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(3): Show | 6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-4154G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049084 | ||||||
chr14:65049125
|
TA | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.956-4097delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65049125 | |||||
chr14:65049125
|
TAA | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0064others(4): Show | 7 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.956-4098_956-4097d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65049125 | |||||
chr14:65049146
|
T | G | 1 | a0001c0001t0002g0134 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.956-4092T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049146 | ||||||
chr14:65049207
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.956-4031A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049207 | ||||||
chr14:65049411
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.956-3827C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049411 | ||||||
chr14:65049462
|
T | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0200a0001c0001t0002g0224 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.956-3776T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049462 | ||||||
chr14:65049911
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.956-3327A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049911 | ||||||
chr14:65050081
|
A | G | 1 | a0001c0001t0001g0349 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.956-3157A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050081 | ||||||
chr14:65050148
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.956-3090T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050148 | ||||||
chr14:65050318
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.956-2920G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050318 | ||||||
chr14:65050388
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 80 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.956-2850C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050388 | ||||||
chr14:65050497
|
A | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0064others(3): Show | 6 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-2741A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050497 | ||||||
chr14:65050570
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.956-2668G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050570 | ||||||
chr14:65050711
|
G | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.956-2527G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050711 | ||||||
chr14:65050824
|
C | T | 24 | a0001c0001t0002g0035a0001c0001t0002g0052a0001c0001t0002g0058others(21): Show | 24 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.956-2414C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050824 | ||||||
chr14:65051007
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.956-2231T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051007 | ||||||
chr14:65051015
|
C | CAGGTGAG others(5): Show |
1 | a0001c0001t0001g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.956-2222_956-2211d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65051015 | |||||
chr14:65051113
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.956-2125T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051113 | ||||||
chr14:65051165
|
C | T | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-2073C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051165 | ||||||
chr14:65051338
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.956-1900G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051338 | ||||||
chr14:65051559
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.956-1679C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051559 | ||||||
chr14:65051567
|
T | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-1671T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051567 | ||||||
chr14:65051588
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.956-1650G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051588 | ||||||
chr14:65051797
|
A | AT | 21 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.956-1426dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65051797 | |||||
chr14:65051857
|
T | A | 3 | a0001c0001t0002g0035a0001c0001t0002g0103a0001c0001t0002g0197 | 3 | HG01891.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.956-1381T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051857 | ||||||
chr14:65051887
|
T | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0348others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-1351T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051887 | ||||||
chr14:65051895
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.956-1343C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051895 | ||||||
chr14:65051940
|
G | A | 5 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0132others(2): Show | 5 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-1298G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051940 | ||||||
chr14:65051949
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.956-1289C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051949 | ||||||
chr14:65051986
|
A | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0260others(2): Show | 5 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-1252A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051986 | ||||||
chr14:65052075
|
A | G | 2 | a0001c0001t0002g0238a0001c0001t0002g0338 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.956-1163A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052075 | ||||||
chr14:65052077
|
A | G | 2 | a0001c0001t0002g0238a0001c0001t0002g0338 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.956-1161A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052077 | ||||||
chr14:65052325
|
T | G | 1 | a0001c0001t0002g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.956-913T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052325 | ||||||
chr14:65052350
|
G | T | 1 | a0001c0001t0002g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.956-888G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052350 | ||||||
chr14:65052384
|
T | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0054others(9): Show | 13 | HG02129.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.956-854T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052384 | ||||||
chr14:65052385
|
A | T | 20 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0118others(17): Show | 20 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.956-853A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052385 | ||||||
chr14:65052418
|
A | C | 1 | a0001c0001t0001g0163 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.956-820A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052418 | ||||||
chr14:65052436
|
T | C | 3 | a0001c0001t0002g0044a0001c0001t0002g0238a0001c0001t0002g0338 | 3 | HG01175.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.956-802T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052436 | ||||||
chr14:65052451
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 210 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.956-787G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052451 | ||||||
chr14:65052517
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0349 | 3 | HG02647.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.956-721G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052517 | ||||||
chr14:65052703
|
A | T | 1 | a0001c0005t0002g0286 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.956-535A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052703 | ||||||
chr14:65052708
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.956-530C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052708 | ||||||
chr14:65052717
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.956-521G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052717 | ||||||
chr14:65052722
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0102 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.956-516A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052722 | ||||||
chr14:65052908
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0344a0001c0001t0002g0351 | 4 | HG02965.hp1 HG03453.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-330C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052908 | ||||||
chr14:65052971
|
T | C | 3 | a0001c0001t0002g0035a0001c0001t0002g0103a0001c0001t0002g0197 | 3 | HG01891.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.956-267T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052971 | ||||||
chr14:65053113
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.956-125A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65053113 | ||||||
chr14:65053122
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.956-116G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65053122 | ||||||
chr14:65053369
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0032a0001c0001t0002g0195 | 3 | HG01361.hp2 HG01928.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1067+20G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053369 | ||||||
chr14:65053377
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1067+28G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053377 | ||||||
chr14:65053528
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 282 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.1067+179T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053528 | ||||||
chr14:65053608
|
G | T | 1 | a0001c0001t0002g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1067+259G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053608 | ||||||
chr14:65053625
|
T | TAAAAAAA others(8): Show |
5 | a0001c0001t0002g0011a0001c0001t0002g0032a0001c0001t0002g0101others(2): Show | 5 | HG01109.hp1 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | ||||||
chr14:65053625
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0002g0044a0001c0001t0002g0109a0001c0001t0002g0294others(1): Show | 4 | HG01175.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | ||||||
chr14:65053625
|
T | TAAAAAAA others(7): Show |
8 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0120others(5): Show | 8 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | ||||||
chr14:65053625
|
T | TAAAAAAA others(8): Show |
34 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(31): Show | 34 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | ||||||
chr14:65053626
|
T | A | 130 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0037others(127): Show | 130 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1067+277T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053626 | ||||||
chr14:65053634
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1067+285A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053634 | ||||||
chr14:65053635
|
C | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(80): Show | 84 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1067+286C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053635 | ||||||
chr14:65053690
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+341T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053690 | ||||||
chr14:65053898
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(199): Show | 205 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.1067+549G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053898 | ||||||
chr14:65054001
|
A | G | 51 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(48): Show | 51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1068-574A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054001 | ||||||
chr14:65054388
|
G | A | 59 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0009others(56): Show | 60 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.1068-187G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054388 | ||||||
chr14:65054440
|
A | C | 51 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(48): Show | 51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1068-135A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054440 | ||||||
chr14:65054443
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1068-132A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054443 | ||||||
chr14:65054468
|
TG | T | 51 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(48): Show | 51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1068-99delG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 65054468 | |||||
chr14:65054832
|
C | T | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+143C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054832 | ||||||
chr14:65054833
|
G | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0032a0001c0001t0002g0120others(1): Show | 4 | HG01361.hp2 HG01928.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+144G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054833 | ||||||
chr14:65054862
|
G | A | 1 | a0001c0001t0002g0314 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1182+173G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054862 | ||||||
chr14:65054910
|
A | C | 1 | a0001c0001t0001g0315 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1182+221A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054910 | ||||||
chr14:65055020
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0348others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+331A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055020 | ||||||
chr14:65055022
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1182+333G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055022 | ||||||
chr14:65055025
|
C | T | 51 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(48): Show | 51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1182+336C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055025 | ||||||
chr14:65055160
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1182+471G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055160 | ||||||
chr14:65055194
|
ATG | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(81): Show | 85 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1182+511_1182+512d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65055194 | |||||
chr14:65055243
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1182+554G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055243 | ||||||
chr14:65055497
|
T | C | 2 | a0001c0001t0002g0095a0001c0001t0002g0126 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1182+808T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055497 | ||||||
chr14:65055504
|
A | T | 9 | a0001c0001t0001g0118a0001c0001t0001g0133a0001c0001t0001g0297others(6): Show | 9 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182+815A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055504 | ||||||
chr14:65055505
|
T | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(201): Show | 207 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.1182+816T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055505 | ||||||
chr14:65055506
|
T | A | 3 | a0001c0001t0002g0035a0001c0001t0002g0103a0001c0001t0002g0197 | 3 | HG01891.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1182+817T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055506 | ||||||
chr14:65055588
|
C | G | 1 | a0001c0001t0002g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1182+899C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055588 | ||||||
chr14:65055696
|
T | C | 72 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0037others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1182+1007T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055696 | ||||||
chr14:65055841
|
A | C | 5 | a0001c0001t0002g0110a0001c0001t0002g0131a0001c0001t0002g0135others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+1152A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055841 | ||||||
chr14:65055944
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1182+1255A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055944 | ||||||
chr14:65055985
|
GT | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1304delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65055985 | |||||
chr14:65056046
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1182+1357C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056046 | ||||||
chr14:65056228
|
CAT | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091others(3): Show | 7 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1540_1182+154 others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056228 | ||||||
chr14:65056269
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+1580A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056269 | ||||||
chr14:65056277
|
A | G | 51 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(48): Show | 51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1182+1588A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056277 | ||||||
chr14:65056297
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(198): Show | 204 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1182+1608G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056297 | ||||||
chr14:65056523
|
A | G | 20 | a0001c0001t0002g0052a0001c0001t0002g0058a0001c0001t0002g0059others(17): Show | 20 | HG02280.hp2 HG02572.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.1182+1834A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056523 | ||||||
chr14:65056544
|
A | G | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1855A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056544 | ||||||
chr14:65056577
|
T | C | 111 | a0001c0001t0001g0072a0001c0001t0002g0003a0001c0001t0002g0006others(108): Show | 112 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(109): Show |
intron_variant | MODIFIER | c.1182+1888T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056577 | ||||||
chr14:65056619
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1182+1930T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056619 | ||||||
chr14:65056635
|
TCTGCCAG others(16): Show |
T | 1 | a0001c0001t0001g0319 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1182+1947_1182+196 others(27): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056635 | ||||||
chr14:65056674
|
G | A | 70 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0010others(67): Show | 71 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1182+1985G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056674 | ||||||
chr14:65056703
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0281 | 2 | NA18969.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1182+2014T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056703 | ||||||
chr14:65056859
|
T | C | 1 | a0001c0001t0002g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1182+2170T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056859 | ||||||
chr14:65057282
|
G | A | 110 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(107): Show | 111 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(108): Show |
intron_variant | MODIFIER | c.1182+2593G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057282 | ||||||
chr14:65057614
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1182+2925G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057614 | ||||||
chr14:65057752
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0348others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3063A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057752 | ||||||
chr14:65057776
|
T | TA | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3089dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65057776 | |||||
chr14:65057782
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1182+3093A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057782 | ||||||
chr14:65057809
|
A | G | 4 | a0001c0001t0002g0029a0001c0001t0002g0031a0001c0001t0002g0036others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3120A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057809 | ||||||
chr14:65057866
|
T | TG | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3178dupG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65057866 | |||||
chr14:65057936
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1183-3245G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057936 | ||||||
chr14:65058110
|
CT | C | 50 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0001t0001g0074others(47): Show | 50 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.1183-3059delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65058110 | |||||
chr14:65058146
|
A | G | 40 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(37): Show | 40 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1183-3035A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058146 | ||||||
chr14:65058201
|
TTTTC | T | 60 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0010others(57): Show | 61 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.1183-2976_1183-297 others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65058201 | |||||
chr14:65058230
|
T | A | 1 | a0001c0001t0001g0220 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1183-2951T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058230 | ||||||
chr14:65058268
|
T | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0238others(1): Show | 4 | HG01081.hp2 HG02109.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-2913T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058268 | ||||||
chr14:65058268
|
T | TC | 36 | a0001c0001t0002g0008a0001c0001t0002g0027a0001c0001t0002g0028others(33): Show | 36 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1183-2912dupC | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65058268 | |||||
chr14:65058270
|
G | A | 68 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0010others(65): Show | 69 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.1183-2911G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058270 | ||||||
chr14:65058270
|
G | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0227 | 2 | HG02165.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1183-2911G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058270 | ||||||
chr14:65058325
|
C | A | 1 | a0001c0001t0001g0336 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1183-2856C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058325 | ||||||
chr14:65058448
|
C | T | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(4): Show | 7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-2733C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058448 | ||||||
chr14:65058523
|
G | C | 110 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(107): Show | 111 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(108): Show |
intron_variant | MODIFIER | c.1183-2658G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058523 | ||||||
chr14:65058540
|
A | G | 112 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(109): Show | 113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-2641A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058540 | ||||||
chr14:65058546
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1183-2635G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058546 | ||||||
chr14:65058612
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1183-2569A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058612 | ||||||
chr14:65058892
|
T | C | 40 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(37): Show | 40 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1183-2289T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058892 | ||||||
chr14:65058895
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1183-2286T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058895 | ||||||
chr14:65059076
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(199): Show | 205 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.1183-2105A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059076 | ||||||
chr14:65059302
|
G | A | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0010others(59): Show | 63 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.1183-1879G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059302 | ||||||
chr14:65059304
|
G | A | 112 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(109): Show | 113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-1877G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059304 | ||||||
chr14:65059334
|
T | C | 112 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(109): Show | 113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-1847T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059334 | ||||||
chr14:65059495
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-1686G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059495 | ||||||
chr14:65059662
|
G | A | 8 | a0001c0001t0002g0079a0001c0001t0002g0101a0001c0001t0002g0108others(5): Show | 8 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1183-1519G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059662 | ||||||
chr14:65059738
|
A | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 6 | HG00408.hp2 HG00609.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183-1443A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059738 | ||||||
chr14:65059810
|
T | TACATATT others(3): Show |
1 | a0001c0001t0001g0319 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1183-1370_1183-136 others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059810 | |||||
chr14:65059837
|
C | CT | 57 | a0001c0001t0001g0072a0001c0001t0001g0145a0001c0001t0001g0161others(54): Show | 57 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.1183-1328dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059837 | |||||
chr14:65059837
|
C | CTT | 59 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0010others(56): Show | 60 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.1183-1329_1183-132 others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059837 | |||||
chr14:65059837
|
CT | C | 68 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1183-1328delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059837 | |||||
chr14:65059855
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1183-1326A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059855 | ||||||
chr14:65059919
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1183-1262C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059919 | ||||||
chr14:65059958
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1183-1223C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059958 | ||||||
chr14:65060056
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1183-1125C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060056 | ||||||
chr14:65060230
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-951A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060230 | ||||||
chr14:65060231
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-950T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060231 | ||||||
chr14:65060233
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-948A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060233 | ||||||
chr14:65060234
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-947A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060234 | ||||||
chr14:65060236
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-945A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060236 | ||||||
chr14:65060241
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-940G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060241 | ||||||
chr14:65060242
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-939G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060242 | ||||||
chr14:65060250
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-931A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060250 | ||||||
chr14:65060251
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-930C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060251 | ||||||
chr14:65060253
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-928A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060253 | ||||||
chr14:65060254
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-927T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060254 | ||||||
chr14:65060256
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-925T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060256 | ||||||
chr14:65060258
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-923T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060258 | ||||||
chr14:65060259
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-922G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060259 | ||||||
chr14:65060261
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-920T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060261 | ||||||
chr14:65060269
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-912T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060269 | ||||||
chr14:65060273
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-908T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060273 | ||||||
chr14:65060274
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-907C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060274 | ||||||
chr14:65060276
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-905C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060276 | ||||||
chr14:65060278
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-903G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060278 | ||||||
chr14:65060279
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-902G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060279 | ||||||
chr14:65060279
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-902G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060279 | ||||||
chr14:65060281
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-900A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060281 | ||||||
chr14:65060282
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-899C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060282 | ||||||
chr14:65060284
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-897A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060284 | ||||||
chr14:65060348
|
G | C | 1 | a0001c0001t0002g0277 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1183-833G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060348 | ||||||
chr14:65060359
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1183-822C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060359 | ||||||
chr14:65060404
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 89 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1183-777C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060404 | ||||||
chr14:65060417
|
T | C | 1 | a0001c0001t0002g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1183-764T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060417 | ||||||
chr14:65060426
|
TAAAAATA others(277): Show |
T | 112 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(109): Show | 113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-740_1183-457d others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060426 | |||||
chr14:65060559
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1183-622A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060559 | ||||||
chr14:65060560
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1183-621G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060560 | ||||||
chr14:65060564
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1183-617C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060564 | ||||||
chr14:65060565
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1183-616G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060565 | ||||||
chr14:65060697
|
C | CAAAAAAA others(1): Show |
66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 67 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1183-473_1183-466d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060697 | |||||
chr14:65060697
|
C | CAAAAAAA others(2): Show |
21 | a0001c0001t0001g0016a0001c0001t0001g0053a0001c0001t0001g0063others(18): Show | 21 | HG00609.hp1 HG01256.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1183-474_1183-466d others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060697 | |||||
chr14:65060697
|
CA | C | 69 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0037others(66): Show | 69 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1183-466delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060697 | |||||
chr14:65060718
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091others(1): Show | 5 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183-463C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060718 | ||||||
chr14:65060766
|
A | G | 1 | a0001c0001t0002g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1183-415A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060766 | ||||||
chr14:65060810
|
T | G | 1 | a0001c0001t0001g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1183-371T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060810 | ||||||
chr14:65060870
|
C | CA | 11 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0080others(8): Show | 11 | HG00621.hp2 HG00735.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-286dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CA | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0033others(8): Show | 11 | HG00438.hp2 HG01106.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.1183-286delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CAA | C | 63 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0041others(60): Show | 63 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1183-287_1183-286d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CAAA | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0057others(10): Show | 13 | HG00408.hp2 HG00609.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1183-288_1183-286d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CAAAA | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(88): Show | 93 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(90): Show |
intron_variant | MODIFIER | c.1183-289_1183-286d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CAAAAA | C | 48 | a0001c0001t0001g0139a0001c0001t0001g0300a0001c0001t0002g0003others(45): Show | 49 | HG00438.hp1 HG00733.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1183-290_1183-286d others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CAAAAAAA | C | 25 | a0001c0001t0002g0007a0001c0001t0002g0044a0001c0001t0002g0058others(22): Show | 25 | HG01175.hp2 HG02109.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1183-292_1183-286d others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0011others(12): Show | 15 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1183-293_1183-286d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060870
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0002g0079a0001c0001t0002g0101a0001c0001t0002g0108others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1183-294_1183-286d others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | |||||
chr14:65060889
|
A | C | 3 | a0001c0001t0001g0304a0001c0001t0001g0319a0001c0001t0001g0346 | 3 | NA18969.hp2 NA19004.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1183-292A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060889 | ||||||
chr14:65060891
|
A | C | 67 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(64): Show | 67 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1183-290A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060891 | ||||||
chr14:65060942
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0091 | 4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-239G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060942 | ||||||
chr14:65060956
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1183-225G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060956 |